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+in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE118336" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE118336.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE118336.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE118336.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# Step 1: Determine if gene expression data is available +# Based on the series description (HTA2.0 array - a gene expression microarray), we assume it contains gene expression data. +is_gene_available = True + +# Step 2: Identify availability of trait, age, and gender, and set row indices accordingly +# From the sample characteristics dictionary: +# { +# 0: ['cell type: iPSC-MN'], +# 1: ['genotype: FUSWT/WT', 'genotype: FUSWT/H517D', 'genotype: FUSH517D/H517D'], +# 2: ['time (differentiation from motor neuron precursor): 2 weeks', 'time (differentiation from motor neuron precursor): 4 weeks'] +# } +# We interpret row=1 as the ALS status (presence/absence of mutation) => trait +trait_row = 1 + +# There's no clear row for age or gender +age_row = None +gender_row = None + +# Step 2.2: Define conversion functions for trait, age, and gender + +def convert_trait(value: str): + # Typically "genotype: something" + parts = value.split(':', 1) + if len(parts) < 2: + return None + val = parts[1].strip() + # Map genotype to binary: "FUSWT/WT" -> 0 (control), else -> 1 (ALS) + if val == "FUSWT/WT": + return 0 + elif "H517D" in val: + return 1 + else: + return None + +def convert_age(value: str): + # Not applicable here, return None + return None + +def convert_gender(value: str): + # Not applicable here, return None + return None + +# Step 3: Initial filtering for dataset usability +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# Step 4: Clinical Feature Extraction (only if trait data is available) +if trait_row is not None: + # Here we assume 'clinical_data' is already loaded as a pandas DataFrame + selected_clinical_df = geo_select_clinical_features( + clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + + # Preview the extracted clinical data + preview = preview_df(selected_clinical_df, n=5) + print("Clinical Data Preview:", preview) + + # Save clinical data to CSV + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on biomedical knowledge, these "xxx_st" identifiers appear to be probe set IDs (likely from an Affymetrix array), +# not human gene symbols. Therefore, they require mapping to gene symbols. + +# Conclusion: +requires_gene_mapping = True +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP 6: Gene Identifier Mapping (Revised) + +# We will attempt to map the probe identifiers in gene_data (e.g. "2824546_st") to those in the +# gene_annotation DataFrame (e.g. "TC01000001.hg.1"). The original attempt concluded there +# was no match and skipped the mapping entirely. Here, we'll demonstrate a more thorough check: +# 1) Direct match +# 2) Partial match by stripping "_st" +# If no matches are found, we conclude that no mapping can be performed and retain the original data. + +# Copy the annotation so we can manipulate it safely +annot_df = gene_annotation.copy() + +# Identify columns to use for probe ID and gene assignment (gene symbol or similar). +probe_col = 'ID' +gene_col = 'gene_assignment' + +# Create the mapping DataFrame +mapping_df = get_gene_mapping( + annotation=annot_df, + prob_col=probe_col, + gene_col=gene_col +) + +# 1) Direct match between expression index and annotation ID: +expr_ids = set(gene_data.index) +annot_ids = set(mapping_df['ID']) +common_ids = expr_ids.intersection(annot_ids) + +if len(common_ids) > 0: + # Some probes match directly; proceed with standard mapping + print("Direct matches found. Proceeding with gene symbol mapping using apply_gene_mapping...") + gene_data = apply_gene_mapping(gene_data, mapping_df) +else: + # 2) Attempt partial match: removing '_st' from expression IDs before checking + print("No direct matches found. Attempting partial match by stripping '_st'...") + # Create a dictionary to map stripped IDs -> original IDs + stripped_to_orig = {} + for idx in gene_data.index: + stripped = idx.replace('_st', '').strip() + stripped_to_orig[stripped] = idx + + # Re-check intersection + new_expr_ids = set(stripped_to_orig.keys()) + common_stripped = new_expr_ids.intersection(annot_ids) + + if len(common_stripped) > 0: + print("Partial matches found. Proceeding with gene symbol mapping...") + # Temporarily rename expression DataFrame index to the stripped version + gene_data_tmp = gene_data.copy() + gene_data_tmp.index = gene_data_tmp.index.map(lambda x: x.replace('_st', '').strip()) + + # Perform mapping with apply_gene_mapping + gene_data_mapped = apply_gene_mapping(gene_data_tmp, mapping_df) + + # We revert the index to some user-friendly format (e.g., the gene symbols returned) + # but "apply_gene_mapping" already sets the new DataFrame's index to gene symbols. + gene_data = gene_data_mapped + else: + # 3) Confirm no mapping possible + print("No direct or partial matches found. No reliable way to map these probe IDs.") + print("Retaining the original gene_data DataFrame without mapping.") + +# Display final shape and top rows +print("Final gene_data shape:", gene_data.shape) +print(gene_data.head(5)) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE26927.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE26927.py new file mode 100644 index 0000000000000000000000000000000000000000..39499a31d2c0049bd4cd983d83def7620186942e --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE26927.py @@ -0,0 +1,207 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" +cohort = "GSE26927" + +# Input paths +in_trait_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis" +in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE26927" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE26927.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE26927.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE26927.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # Based on the series summary, this dataset uses Illumina whole genome array. + +# 2. Variable Availability +# Checking the sample characteristics dictionary, we found: +# - trait_row = 0, because row 0 has "disease: ..." entries including "Amyotrophic lateral sclerosis". +# - age_row = 2, because row 2 has "age at death (in years): ..." entries. +# - gender_row = 1, because row 1 has "gender: M" or "gender: F". +trait_row = 0 +age_row = 2 +gender_row = 1 + +# 2.2 Data Type Conversions +def convert_trait(value: str) -> int: + """ + Convert disease field to binary indicating ALS (1) vs non-ALS (0). + Unknown values are converted to None. + Example input: "disease: Amyotrophic lateral sclerosis" + """ + parts = value.split(":") + if len(parts) < 2: + return None + disease_str = parts[1].strip().lower() + if "amyotrophic lateral sclerosis" in disease_str: + return 1 + else: + return 0 + +def convert_age(value: str) -> Optional[float]: + """ + Convert age field to continuous (float). + Unknown values are converted to None. + Example input: "age at death (in years): 70" + """ + parts = value.split(":") + if len(parts) < 2: + return None + age_str = parts[1].strip() + try: + return float(age_str) + except ValueError: + return None + +def convert_gender(value: str) -> Optional[int]: + """ + Convert gender field to binary: female -> 0, male -> 1. + Unknown values are converted to None. + Example input: "gender: M" + """ + parts = value.split(":") + if len(parts) < 2: + return None + gender_str = parts[1].strip().lower() + if gender_str == 'f': + return 0 + elif gender_str == 'm': + return 1 + else: + return None + +# 3. Save Metadata (initial filtering) +is_trait_available = (trait_row is not None) +is_final = False # initial filtering +validate_and_save_cohort_info( + is_final=is_final, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction (only if trait_row is not None) +if trait_row is not None: + # Assume 'clinical_data' is the DataFrame with sample characteristics loaded from a previous step. + selected_clinical_df = geo_select_clinical_features( + clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + # Preview and save + print("Preview of Selected Clinical Features:", preview_df(selected_clinical_df)) + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These identifiers, such as 'ILMN_10000', are Illumina microarray probe IDs rather than standard gene symbols. +# Hence, they require mapping to gene symbols. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify the corresponding columns for probe ID and gene symbol in 'gene_annotation'. +# From the previews, 'ID' matches the probe identifiers used in the gene expression data (e.g., 'ILMN_10000'), +# and 'SYMBOL' stores the gene symbols. +probe_col = 'ID' +symbol_col = 'SYMBOL' + +# 2. Get a mapping dataframe from 'gene_annotation'. +mapping_df = get_gene_mapping(gene_annotation, prob_col=probe_col, gene_col=symbol_col) + +# 3. Convert probe-level measurements to gene-level expression data using 'apply_gene_mapping'. +# This handles the many-to-many relationships by dividing expression across genes and summing contributions per gene. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# For verification, let's output a small preview of the resulting gene_data: shape and first few gene indices. +print("Mapped gene_data shape:", gene_data.shape) +print("First 10 genes after mapping:", gene_data.index[:10].to_list()) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Read the previously saved clinical data and correctly restore the row/column structure +# After step 2, the CSV has 3 rows (trait, Age, Gender) and columns = sample IDs (header=0). +# We can directly set the new index labels because we know row 0 = trait, row 1 = Age, row 2 = Gender. +selected_clinical_df = pd.read_csv(out_clinical_data_file, header=0) +if selected_clinical_df.shape[0] == 3: + selected_clinical_df.index = [trait, 'Age', 'Gender'] +else: + print("Warning: The clinical data does not have 3 rows as expected. Check the saved CSV format.") + +# 3. Link clinical and gene expression data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 4. Handle missing values (drop samples missing trait, drop high-missing genes/samples, impute remaining) +linked_data = handle_missing_values(linked_data, trait_col=trait) + +# 5. Check for biased features (trait, age, gender) and remove biased demographic features +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 6. Final quality validation and metadata saving +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Final data pipeline completed." +) + +# 7. Save final linked data if usable +if is_usable: + linked_data.to_csv(out_data_file) + print(f"Saved final linked data to {out_data_file}") +else: + print("Dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE52937.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE52937.py new file mode 100644 index 0000000000000000000000000000000000000000..b0b787fdf8786788b227915c9925e386e430044c --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE52937.py @@ -0,0 +1,141 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" +cohort = "GSE52937" + +# Input paths +in_trait_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis" +in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE52937" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE52937.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE52937.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE52937.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # Based on background ("transcriptional response", etc.), we assume gene expression data is present + +# 2. Variable Availability and Data Type Conversion + +# From the sample characteristics dictionary, no rows contain explicit or implicit ALS trait, age, or gender data. +trait_row = None +age_row = None +gender_row = None + +# Define data conversion functions (they won't be used if the rows are None, but we define them as requested). + +def convert_trait(value: str) -> int: + # Example logic for binary classification of the trait + # If the trait is unavailable, return None + return None + +def convert_age(value: str) -> float: + # Example logic for continuous age value + return None + +def convert_gender(value: str) -> int: + # Example logic for binary gender classification + return None + +# 3. Save Metadata (Initial Filtering) +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# We only do this if trait_row is not None. Here trait_row is None, so we skip this step. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1 & 2. Identify the corresponding columns in the gene annotation dataframe for +# (a) the probe IDs, which match those in the gene expression data +# (b) the gene symbols +# We use "ID" for the probe identifier and "Symbol" for the gene symbol. +mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Symbol") + +# 3. Convert probe-level data in gene_data to gene-level data using the mapping. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# For confirmation, let's print out the shape of the resulting gene_data +print("Mapped gene_data shape:", gene_data.shape) +# STEP 7: Data Normalization and Linking + +# Since we concluded in previous steps that there is no trait data (trait_row = None), +# we cannot link clinical data or perform trait-based analyses. We'll still normalize +# the gene data and then perform a final validation indicating that the dataset does +# not have trait information. + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. No trait data is available, so we skip linking genetic and clinical data. +# We also skip handling missing trait values or checking trait bias. + +# 3. Final Quality Validation +# Since there's no trait, is_trait_available=False, so the dataset won't be deemed usable for trait-based analysis. +# However, we still record the metadata. We must provide 'df' and 'is_biased' as the function requires. +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, + is_biased=False, # Arbitrarily False because trait doesn't exist + df=normalized_gene_data, # We'll pass the gene data as the 'df' + note="No trait data available, so cohort is not usable for association study." +) + +# 4. If the dataset were usable, we'd save the final linked data. In this case, it's not usable for trait-based association. +if is_usable: + # This branch will not execute because there's no trait + linked_data.to_csv(out_data_file) + print(f"Saved final linked data to {out_data_file}") +else: + print("Trait data not available. Skipping final output for association analysis.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE61322.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE61322.py new file mode 100644 index 0000000000000000000000000000000000000000..7f055a8882cc9c754fe132e605a06e70176f205d --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE61322.py @@ -0,0 +1,150 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" +cohort = "GSE61322" + +# Input paths +in_trait_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis" +in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE61322" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE61322.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE61322.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE61322.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +# From the background info ("microarray", "RNA-sequencing"), this dataset likely contains gene expression data. +is_gene_available = True + +# 2. Variable Availability and Conversion +# Checking the sample characteristics dictionary: +# {0: ['diagnosis: carrier', 'diagnosis: affected'], +# 1: ['disease: AOA2'], +# 2: ['definite analysis: definite', 'definite analysis: presumed']} +# None of these keys mention "Amyotrophic_Lateral_Sclerosis" or an "ALS" variant. +# Also, no keys show age or gender data. Hence, all are considered unavailable. +trait_row = None +age_row = None +gender_row = None + +def convert_trait(value: str) -> Optional[float]: + # Not used as trait_row is None, but we provide a stub. + # Typically would parse the string after ':', then map to 0./1. or None appropriately. + return None + +def convert_age(value: str) -> Optional[float]: + # Not used as age_row is None, but we provide a stub. + return None + +def convert_gender(value: str) -> Optional[int]: + # Not used as gender_row is None, but we provide a stub. + return None + +# 3. Save Metadata with initial filtering +# If trait_row is None => is_trait_available = False +is_trait_available = (trait_row is not None) + +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, we skip this step (no clinical data for the trait). +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the above identifiers (e.g., ILMN_1343291, ILMN_1651209, etc.), +# they are Illumina probe IDs rather than standard human gene symbols. +# Therefore, they require mapping to gene symbols. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. From the annotation preview and the gene expression row IDs, we see that +# the "ID" column in gene_annotation matches probe IDs like "ILMN_1343291", +# and the "Symbol" column stores the gene symbols. +prob_col = "ID" +gene_col = "Symbol" + +# 2. Extract the mapping dataframe with these two columns +mapping_df = get_gene_mapping(gene_annotation, prob_col, gene_col) + +# 3. Apply the mapping to convert probe-level data into gene-level expression +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +# Since we concluded in previous steps that there is no trait data (trait_row = None), +# we cannot link clinical data or perform trait-based analyses. We'll still normalize +# the gene data and then perform a final validation indicating that the dataset does +# not have trait information. + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. No trait data is available, so we skip linking genetic and clinical data. +# We also skip handling missing trait values or checking trait bias. + +# 3. Final Quality Validation +# Since there's no trait, is_trait_available=False, so the dataset won't be deemed usable for trait-based analysis. +# However, we still record the metadata. We must provide 'df' and 'is_biased' as the function requires. +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, + is_biased=False, # Arbitrarily False because trait doesn't exist + df=normalized_gene_data, # We'll pass the gene data as the 'df' + note="No trait data available, so cohort is not usable for association study." +) + +# 4. If the dataset were usable, we'd save the final linked data. In this case, it's not usable for trait-based association. +if is_usable: + # This branch will not execute because there's no trait + linked_data.to_csv(out_data_file) + print(f"Saved final linked data to {out_data_file}") +else: + print("Trait data not available. Skipping final output for association analysis.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE68608.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE68608.py new file mode 100644 index 0000000000000000000000000000000000000000..0df1526530a9602703cb4698d48d8da3403c91d5 --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE68608.py @@ -0,0 +1,157 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" +cohort = "GSE68608" + +# Input paths +in_trait_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis" +in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE68608" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE68608.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68608.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE68608.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1) Gene Expression Data Availability +is_gene_available = True # Based on the background, it's likely gene expression data. + +# 2) Variable Availability and Data Type Conversion +trait_row = 1 # Key 1 contains ALS vs Control information. +age_row = None # No age information found in the dictionary. +gender_row = None # No gender information found in the dictionary. + +def convert_trait(value: str): + # Extract the part after the colon (if any) and convert to lowercase + if ':' in value: + _, val = value.split(':', 1) + val = val.strip().lower() + else: + val = value.strip().lower() + + # Map to binary + if 'als' in val: + return 1 + elif 'control' in val or 'healthy' in val: + return 0 + else: + return None + +def convert_age(value: str): + # No age data is available; return None + return None + +def convert_gender(value: str): + # No gender data is available; return None + return None + +# 3) Save Metadata (Initial filtering) +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4) Clinical Feature Extraction (only if trait data is available) +if trait_row is not None: + selected_clinical_df = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + print("Preview of selected clinical features:") + print(preview_df(selected_clinical_df)) + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the provided identifiers (e.g., '1007_s_at', '1053_at'), they appear to be Affymetrix probe set IDs. +# These are not standard human gene symbols and thus require mapping to gene symbols. +print("They appear to be Affymetrix probe set IDs.") +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1) The 'ID' column in 'gene_annotation' corresponds to the probe IDs in the gene expression data. +# The 'Gene Symbol' column contains the gene symbols. +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Gene Symbol') + +# 2) Convert probe-level measurements to gene-level measurements by applying the many-to-many mapping. +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Systematically handle missing values +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and demographic features) are severely biased +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Trait data is ALS vs. control; age and gender are not available." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file) + print(f"Saved final linked data to {out_data_file}") +else: + print("Data not usable for association; skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE95810.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE95810.py new file mode 100644 index 0000000000000000000000000000000000000000..92a504bcefe256ed38b16c815f09118674f5c8fb --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/GSE95810.py @@ -0,0 +1,105 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" +cohort = "GSE95810" + +# Input paths +in_trait_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis" +in_cohort_dir = "../DATA/GEO/Amyotrophic_Lateral_Sclerosis/GSE95810" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/GSE95810.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/GSE95810.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/GSE95810.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1) Determine if gene expression data is available +is_gene_available = True # Based on series title indicating "Gene expression..." + +# 2) Identify the availability of trait, age, and gender data +trait_row = None # No ALS-specific indicator in the sample characteristics +age_row = None # No age data found +gender_row = None # No gender data found + +# 2) Create conversion functions (though they won't be used since rows are None) +def convert_trait(value: str): + return None + +def convert_age(value: str): + return None + +def convert_gender(value: str): + return None + +# 3) Initial metadata saving and validation +is_trait_available = (trait_row is not None) +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4) Skip clinical feature extraction because 'trait_row' is None +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the provided gene identifiers (e.g., A1BG, A1CF, A2M, etc.), they appear to be standard human gene symbols. +# Consequently, a separate mapping step does not seem to be required. + +print("requires_gene_mapping = False") +# STEP 5: Data Normalization and Linking + +# Since trait data is not available based on the previous steps (trait_row=None), +# we cannot perform clinical-gene linking or meaningful trait-based analyses. + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2-6. Since there's no trait data, we skip linking and final output for association. +# Perform final validation indicating the dataset is not usable for trait association. +is_trait_available = False +validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=is_trait_available, + is_biased=False, # Provide a valid Boolean so it doesn't raise ValueError + df=pd.DataFrame(), # Empty since we can't link without trait + note="No trait data found; skipping linking and final output." +) + +print("Trait data is unavailable; no further steps for linking or final output can be performed.") \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/TCGA.py b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..a7d1dc055dda34f5ced91a2f940522884077f937 --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Amyotrophic_Lateral_Sclerosis" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Amyotrophic_Lateral_Sclerosis/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE118336.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE118336.csv new file mode 100644 index 0000000000000000000000000000000000000000..b467f55a3faf394e64204c43920fbdb0790762ae --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE118336.csv @@ -0,0 +1 @@ +Gene,GSM3325490,GSM3325491,GSM3325492,GSM3325493,GSM3325494,GSM3325495,GSM3325496,GSM3325497,GSM3325498,GSM3325499,GSM3325500,GSM3325501,GSM3325502,GSM3325503,GSM3325504,GSM3325505,GSM3325506,GSM3325507,GSM3325508,GSM3325509,GSM3325510,GSM3325511,GSM3325512,GSM3325513,GSM3325514,GSM3325515,GSM3325516,GSM3325517,GSM3325518,GSM3325519,GSM3325520,GSM3325521,GSM3325522,GSM3325523,GSM3325524,GSM3325525,GSM3325526,GSM3325527,GSM3325528,GSM3325529,GSM3325530,GSM3325531,GSM3325532,GSM3325533,GSM3325534,GSM3325535,GSM3325536,GSM3325537,GSM3325538,GSM3325539,GSM3325540,GSM3325541,GSM3325542,GSM3325543,GSM3325544,GSM3325545,GSM3325546,GSM3325547,GSM3325548,GSM3325549 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE139384.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE139384.csv new file mode 100644 index 0000000000000000000000000000000000000000..60ba15b60076d9b3d13c09c4ee1c941ca23bfcac --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE139384.csv @@ -0,0 +1 @@ +Gene,GSM4140293,GSM4140294,GSM4140295,GSM4140296,GSM4140297,GSM4140298,GSM4140299,GSM4140300,GSM4140301,GSM4140302,GSM4140303,GSM4140304,GSM4140305,GSM4140306,GSM4140307,GSM4140308,GSM4140309,GSM4140310,GSM4140311,GSM4140312,GSM4140313,GSM4140314,GSM4140315,GSM4140316,GSM4140317,GSM4140318,GSM4140319,GSM4140320,GSM4140321,GSM4140322,GSM4140323,GSM4140324,GSM4140325 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE212134.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE212134.csv new file mode 100644 index 0000000000000000000000000000000000000000..2ef4e2968c51949fe26dc2fb9c16e74b0ea446f0 --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE212134.csv @@ -0,0 +1 @@ +Gene,GSM6509811,GSM6509812,GSM6509813,GSM6509814,GSM6509815,GSM6509816,GSM6509817,GSM6509818,GSM6509819,GSM6509820,GSM6509821,GSM6509822,GSM6509823,GSM6509824,GSM6509825,GSM6509826,GSM6509827,GSM6509828,GSM6509829,GSM6509830,GSM6509831,GSM6509832,GSM6509833,GSM6509834,GSM6509835,GSM6509836,GSM6509837,GSM6509838,GSM6509839,GSM6509840,GSM6509841,GSM6509842,GSM6509843,GSM6509844,GSM6509845,GSM6509846,GSM6509847,GSM6509848,GSM6509849,GSM6509850,GSM6509851,GSM6509852 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE26927.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE26927.csv new file mode 100644 index 0000000000000000000000000000000000000000..11d46559547b25539c091edc7b40e6bf3659f36f --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE26927.csv @@ -0,0 +1 @@ +Gene,GSM663008,GSM663009,GSM663010,GSM663011,GSM663012,GSM663013,GSM663014,GSM663015,GSM663016,GSM663017,GSM663018,GSM663019,GSM663020,GSM663021,GSM663022,GSM663023,GSM663024,GSM663025,GSM663026,GSM663027,GSM663028,GSM663029,GSM663030,GSM663031,GSM663032,GSM663033,GSM663034,GSM663035,GSM663036,GSM663037,GSM663038,GSM663039,GSM663040,GSM663041,GSM663042,GSM663043,GSM663044,GSM663045,GSM663046,GSM663047,GSM663048,GSM663049,GSM663050,GSM663051,GSM663052,GSM663053,GSM663054,GSM663055,GSM663056,GSM663057,GSM663058,GSM663059,GSM663060,GSM663061,GSM663062,GSM663063,GSM663064,GSM663065,GSM663066,GSM663067,GSM663068,GSM663069,GSM663070,GSM663071,GSM663072,GSM663073,GSM663074,GSM663075,GSM663076,GSM663077,GSM663078,GSM663079,GSM663080,GSM663081,GSM663082,GSM663083,GSM663084,GSM663085,GSM663086,GSM663087,GSM663088,GSM663089,GSM663090,GSM663091,GSM663092,GSM663093,GSM663094,GSM663095,GSM663096,GSM663097,GSM663098,GSM663099,GSM663100,GSM663101,GSM663102,GSM663103,GSM663104,GSM663105,GSM663106,GSM663107,GSM663108,GSM663109,GSM663110,GSM663111,GSM663112,GSM663113,GSM663114,GSM663115,GSM663116,GSM663117,GSM663118,GSM663119,GSM663120,GSM663121,GSM663122,GSM663123,GSM663124,GSM663125 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE52937.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE52937.csv new file mode 100644 index 0000000000000000000000000000000000000000..9b167f5f628a2808143d4d598ad36f02a0fc03ce --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE52937.csv @@ -0,0 +1 @@ +Gene,GSM1278303,GSM1278304,GSM1278305,GSM1278306,GSM1278307,GSM1278308,GSM1278309,GSM1278310,GSM1278311,GSM1278312,GSM1278313,GSM1278314,GSM1278315,GSM1278316,GSM1278317,GSM1278318,GSM1278319,GSM1278320,GSM1278321,GSM1278322,GSM1278323,GSM1278324,GSM1278325,GSM1278326,GSM1278327,GSM1278328,GSM1278329,GSM1627269,GSM1627270,GSM1627271,GSM1627272,GSM1627273,GSM1627274,GSM1627275,GSM1627276,GSM1627277,GSM1627278,GSM1627279,GSM1627280,GSM1627281,GSM1627282,GSM1627283,GSM1627284,GSM1627285,GSM1627286,GSM1627287,GSM1627288,GSM1627289,GSM1627290,GSM1627291,GSM1627292,GSM1627293,GSM1627294,GSM1627295 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE61322.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE61322.csv new file mode 100644 index 0000000000000000000000000000000000000000..359accbeb9cf4e8727672f9e18ff991b9742d83d --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE61322.csv @@ -0,0 +1 @@ +Gene,GSM1502059,GSM1502060,GSM1502061,GSM1502062,GSM1502063,GSM1502064,GSM1502065,GSM1502066,GSM1502067,GSM1502068,GSM1502069,GSM1502070,GSM1502071,GSM1502072,GSM1502073,GSM1502074,GSM1502075,GSM1502076,GSM1502077,GSM1502078,GSM1502079,GSM1502080,GSM1502081,GSM1502082,GSM1502083,GSM1502084,GSM1502085,GSM1502086,GSM1502087,GSM1502088,GSM1502089,GSM1502090,GSM1502091 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68607.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68607.csv new file mode 100644 index 0000000000000000000000000000000000000000..33002a819e5cd4c23438ac3170b890fe2487c144 --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68607.csv @@ -0,0 +1 @@ +Gene,GSM1677001,GSM1677002,GSM1677003,GSM1677004,GSM1677005,GSM1677006,GSM1677007,GSM1677008,GSM1677009,GSM1677010,GSM1677011,GSM1677012,GSM1677013,GSM1677014,GSM1677015,GSM1677016,GSM1677017,GSM1677018,GSM1677019,GSM1677020,GSM1677021,GSM1677022,GSM1677023,GSM1677024,GSM1677025,GSM1677026,GSM1677027,GSM1677028,GSM1677029,GSM1677030,GSM1677031,GSM1677032,GSM1677033,GSM1677034,GSM1677035,GSM1677036,GSM1677037,GSM1677038,GSM1677039,GSM1677040,GSM1677041,GSM1677042,GSM1677043,GSM1677044,GSM1677045,GSM1677046,GSM1677047,GSM1677048,GSM1677049,GSM1677050,GSM1677051,GSM1677052,GSM1677053,GSM1677054,GSM1677055,GSM1677056,GSM1677057,GSM1677058,GSM1677059,GSM1677060,GSM1677061,GSM1677062,GSM1677063,GSM1677064,GSM1677065,GSM1677066,GSM1677067,GSM1677068,GSM1677069 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68608.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68608.csv new file mode 100644 index 0000000000000000000000000000000000000000..55d7bf31fab22d56317f895c1cc8ea409ca6ae9b --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE68608.csv @@ -0,0 +1 @@ +Gene,GSM1676853,GSM1676854,GSM1676855,GSM1676856,GSM1676857,GSM1676858,GSM1676859,GSM1676860,GSM1676861,GSM1676862,GSM1676863 diff --git a/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE95810.csv b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE95810.csv new file mode 100644 index 0000000000000000000000000000000000000000..31e5584e3f019cef6e6ccb4b44bbd2dc0821de79 --- /dev/null +++ b/p1/preprocess/Amyotrophic_Lateral_Sclerosis/gene_data/GSE95810.csv @@ -0,0 +1 @@ +ID,GSM2526327,GSM2526328,GSM2526329,GSM2526330,GSM2526331,GSM2526332,GSM2526333,GSM2526334,GSM2526335,GSM2526336,GSM2526337,GSM2526338,GSM2526339,GSM2526340,GSM2526341,GSM2526342,GSM2526343,GSM2526344,GSM2526345,GSM2526346,GSM2526347,GSM2526348,GSM2526349,GSM2526350,GSM2526351,GSM2526352,GSM2526353,GSM2526354,GSM2526355,GSM2526356,GSM2526357,GSM2526358,GSM2526359,GSM2526360,GSM2526361,GSM2526362,GSM2526363,GSM2526364,GSM2526365,GSM2526366,GSM2526367,GSM2526368,GSM2526369,GSM2526370,GSM2526371,GSM2526372,GSM2526373,GSM2526374,GSM2526375,GSM2526376,GSM2526377,GSM2526378,GSM2526379,GSM2526380,GSM2526381,GSM2526382,GSM2526383,GSM2526384 diff --git a/p1/preprocess/Angelman_Syndrome/code/GSE43900.py b/p1/preprocess/Angelman_Syndrome/code/GSE43900.py new file mode 100644 index 0000000000000000000000000000000000000000..9dc3661b9c4d6575bd5094d247fbdaed1f5a3258 --- /dev/null +++ b/p1/preprocess/Angelman_Syndrome/code/GSE43900.py @@ -0,0 +1,169 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Angelman_Syndrome" +cohort = "GSE43900" + +# Input paths +in_trait_dir = "../DATA/GEO/Angelman_Syndrome" +in_cohort_dir = "../DATA/GEO/Angelman_Syndrome/GSE43900" + +# Output paths +out_data_file = "./output/preprocess/1/Angelman_Syndrome/GSE43900.csv" +out_gene_data_file = "./output/preprocess/1/Angelman_Syndrome/gene_data/GSE43900.csv" +out_clinical_data_file = "./output/preprocess/1/Angelman_Syndrome/clinical_data/GSE43900.csv" +json_path = "./output/preprocess/1/Angelman_Syndrome/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Determine if the dataset likely contains gene expression data +is_gene_available = True # From background info, it appears to focus on gene regulation, so we assume gene expression data + +# 2. Variable Availability and Data Type Conversion + +# According to the sample characteristics dictionary, we only have: +# 0: treatment information, +# 1: cell type, and +# 2: strain. +# None indicates that the dataset does not provide suitable human trait, age, or gender info. +trait_row = None +age_row = None +gender_row = None + +# Define the conversion functions (though they won't be used if rows are None). + +def convert_trait(x: str) -> int: + # No actual data available, placeholder implementation + return None + +def convert_age(x: str) -> float: + # No actual data available, placeholder implementation + return None + +def convert_gender(x: str) -> int: + # No actual data available, placeholder implementation + return None + +# 3. Save Metadata (initial filtering) +is_trait_available = (trait_row is not None) +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction (skip because trait_row is None) +# No action needed as trait_row is None +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on observation, the identifiers are numeric probe IDs and do not appear to be standard human gene symbols. +# Therefore, gene mapping is required. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Decide the columns for gene identifier (probe) and gene symbol based on the preview. +probe_col = "ID" +gene_symbol_col = "Gene Symbol" + +# 2. Get the mapping dataframe from the annotation. +mapping_df = get_gene_mapping(gene_annotation, probe_col, gene_symbol_col) + +# 3. Convert probe-level measurements to gene-level expression data. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# Display the first few gene symbols to confirm the result. +print(gene_data.index[:20]) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Check if the trait is available in this dataset +if trait_row is None: + # If the trait does not exist, we do not finalize; we do an initial validation + # so that the library won't require 'df' and 'is_biased'. + validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=True, # Genetic data is present + is_trait_available=False # Trait data is not available + ) + print("Trait data not available. Only gene expression data was processed. No final data to save.") + +else: + # 3. Since trait is available, link the clinical and genetic data on sample IDs + selected_clinical_df = geo_select_clinical_features( + clinical_data, + trait, + trait_row, + convert_trait, + age_row, + convert_age, + gender_row, + convert_gender + ) + linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + + # 4. Handle missing values as instructed + linked_data = handle_missing_values(linked_data, trait) + + # 5. Determine whether the trait is severely biased + trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + + # 6. Conduct final quality validation and save metadata + is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." + ) + + # 7. If the dataset is usable, save the final linked data + if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") + else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Angelman_Syndrome/code/TCGA.py b/p1/preprocess/Angelman_Syndrome/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..a3256b3990c4e07b508270df5301a5e47225516f --- /dev/null +++ b/p1/preprocess/Angelman_Syndrome/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Angelman_Syndrome" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Angelman_Syndrome/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Angelman_Syndrome/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Angelman_Syndrome/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Angelman_Syndrome/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Angelman_Syndrome/cohort_info.json b/p1/preprocess/Angelman_Syndrome/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..0a5023522d9ffefba33d85c60fb8fa9ccdd0714c --- /dev/null +++ b/p1/preprocess/Angelman_Syndrome/cohort_info.json @@ -0,0 +1 @@ +{"GSE43900": {"is_usable": false, "is_gene_available": true, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}} \ No newline at end of file diff --git a/p1/preprocess/Angelman_Syndrome/gene_data/GSE43900.csv b/p1/preprocess/Angelman_Syndrome/gene_data/GSE43900.csv new file mode 100644 index 0000000000000000000000000000000000000000..b0e0856dacf91d400f285bd579adfc9cbb904783 --- /dev/null +++ b/p1/preprocess/Angelman_Syndrome/gene_data/GSE43900.csv @@ -0,0 +1 @@ +Gene,GSM1179395,GSM1179396,GSM1179397,GSM1179398,GSM1179399,GSM1179400,GSM1179401,GSM1179402,GSM1179409,GSM1179410,GSM1179411,GSM1179412,GSM1179413,GSM1179414,GSM1179415,GSM1179416,GSM1179417,GSM1179418,GSM1179419,GSM1179420,GSM1179421,GSM1179422,GSM1179423,GSM1179424,GSM1179425,GSM1179426,GSM1179427,GSM1179428,GSM1179429,GSM1179430,GSM1179431,GSM1179432,GSM1179433,GSM1179434 diff --git a/p1/preprocess/Aniridia/clinical_data/GSE137996.csv b/p1/preprocess/Aniridia/clinical_data/GSE137996.csv new file mode 100644 index 0000000000000000000000000000000000000000..f859b3fc09d15da2181e0af82cf4107962359144 --- /dev/null +++ b/p1/preprocess/Aniridia/clinical_data/GSE137996.csv @@ -0,0 +1,4 @@ +GSM4096389,GSM4096390,GSM4096391,GSM4096392,GSM4096393,GSM4096394,GSM4096395,GSM4096396,GSM4096397,GSM4096398,GSM4096399,GSM4096400,GSM4096401,GSM4096402,GSM4096403,GSM4096404,GSM4096405,GSM4096406,GSM4096407,GSM4096408,GSM4096409,GSM4096410,GSM4096411,GSM4096412,GSM4096413,GSM4096414,GSM4096415,GSM4096416,GSM4096417,GSM4096418,GSM4096419,GSM4096420,GSM4096421,GSM4096422,GSM4096423,GSM4096424,GSM4096425,GSM4096426,GSM4096427,GSM4096428 +1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0 +20.0,20.0,28.0,20.0,38.0,57.0,26.0,18.0,36.0,42.0,18.0,42.0,36.0,28.0,55.0,54.0,34.0,51.0,46.0,52.0,53.0,54.0,40.0,55.0,57.0,28.0,39.0,59.0,20.0,32.0,37.0,34.0,28.0,28.0,29.0,19.0,25.0,25.0,34.0,22.0 +0.0,0.0,0.0,0.0,0.0,1.0,0.0,1.0,0.0,0.0,0.0,0.0,1.0,0.0,0.0,1.0,1.0,0.0,0.0,0.0,0.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,0.0,0.0,0.0,1.0,0.0,0.0,1.0,0.0,0.0 diff --git a/p1/preprocess/Aniridia/clinical_data/GSE137997.csv b/p1/preprocess/Aniridia/clinical_data/GSE137997.csv new file mode 100644 index 0000000000000000000000000000000000000000..c265871ba0382239ba1f653d4e4740af3880aa57 --- /dev/null +++ b/p1/preprocess/Aniridia/clinical_data/GSE137997.csv @@ -0,0 +1,4 @@ +GSM4096349,GSM4096350,GSM4096351,GSM4096352,GSM4096353,GSM4096354,GSM4096355,GSM4096356,GSM4096357,GSM4096358,GSM4096359,GSM4096360,GSM4096361,GSM4096362,GSM4096363,GSM4096364,GSM4096365,GSM4096366,GSM4096367,GSM4096368,GSM4096369,GSM4096370,GSM4096371,GSM4096372,GSM4096373,GSM4096374,GSM4096375,GSM4096376,GSM4096377,GSM4096378,GSM4096379,GSM4096380,GSM4096381,GSM4096382,GSM4096383,GSM4096384,GSM4096385,GSM4096386,GSM4096387,GSM4096388 +1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0 +20.0,20.0,28.0,20.0,38.0,57.0,26.0,18.0,36.0,42.0,18.0,42.0,36.0,28.0,55.0,54.0,34.0,51.0,46.0,52.0,53.0,54.0,40.0,55.0,57.0,28.0,39.0,59.0,20.0,32.0,37.0,34.0,28.0,28.0,29.0,19.0,25.0,25.0,34.0,22.0 +0.0,0.0,0.0,0.0,0.0,1.0,0.0,1.0,0.0,0.0,0.0,0.0,1.0,0.0,0.0,1.0,1.0,0.0,0.0,0.0,0.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,0.0,0.0,0.0,1.0,0.0,0.0,1.0,0.0,0.0 diff --git a/p1/preprocess/Aniridia/code/GSE137996.py b/p1/preprocess/Aniridia/code/GSE137996.py new file mode 100644 index 0000000000000000000000000000000000000000..88b4547a9fadd85ce3e3f65be5505297cb01cfce --- /dev/null +++ b/p1/preprocess/Aniridia/code/GSE137996.py @@ -0,0 +1,170 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Aniridia" +cohort = "GSE137996" + +# Input paths +in_trait_dir = "../DATA/GEO/Aniridia" +in_cohort_dir = "../DATA/GEO/Aniridia/GSE137996" + +# Output paths +out_data_file = "./output/preprocess/1/Aniridia/GSE137996.csv" +out_gene_data_file = "./output/preprocess/1/Aniridia/gene_data/GSE137996.csv" +out_clinical_data_file = "./output/preprocess/1/Aniridia/clinical_data/GSE137996.csv" +json_path = "./output/preprocess/1/Aniridia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# Step 1: Determine if gene expression data is available +# Based on the background info (mRNA expression and microRNA data), we consider this dataset to have gene expression data. +is_gene_available = True + +# Step 2: Identify availability for trait, age, and gender, and define conversion functions. + +# From the sample characteristics: +# row 0 => age +# row 1 => gender +# row 2 => disease (AAK / healthy control) +# +# We treat 'disease' as the trait variable, 'age' as continuous, and 'gender' as binary. + +trait_row = 2 +age_row = 0 +gender_row = 1 + +def convert_trait(x: str) -> int: + # Extract the raw value after the colon + val = x.split(':')[-1].strip().lower() + # Convert to binary: 1 for aniridia (AAK), 0 for control, None otherwise + if val == 'aak': + return 1 + elif val == 'healthy control': + return 0 + return None + +def convert_age(x: str) -> float: + # Extract the raw value after the colon + val = x.split(':')[-1].strip() + # Convert to float if possible + try: + return float(val) + except ValueError: + return None + +def convert_gender(x: str) -> int: + # Extract the raw value after the colon + val = x.split(':')[-1].strip().lower() + # Convert F/M/W to binary: female => 0, male => 1 + if val in ['f', 'w']: + return 0 + elif val == 'm': + return 1 + return None + +# Step 3: Initial filtering and saving metadata +is_trait_available = (trait_row is not None) + +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# Step 4: Clinical feature extraction (only if trait_row is not None) +if trait_row is not None: + selected_clinical_df = geo_select_clinical_features( + clinical_data, + trait=trait, # "Aniridia" + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + + # Preview extracted clinical features + previewed_data = preview_df(selected_clinical_df) + print("Preview of selected clinical data:", previewed_data) + + # Save clinical features to CSV + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# After reviewing the identifiers such as "A_19_P00315452", they appear to be array probe IDs and not standard gene symbols. +# Therefore, gene symbol mapping is required. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# Gene Identifier Mapping +mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="GENE_SYMBOL") +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Aniridia/code/GSE137997.py b/p1/preprocess/Aniridia/code/GSE137997.py new file mode 100644 index 0000000000000000000000000000000000000000..971e35f23888adaa1b609c6ff1d0eec471f18094 --- /dev/null +++ b/p1/preprocess/Aniridia/code/GSE137997.py @@ -0,0 +1,167 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Aniridia" +cohort = "GSE137997" + +# Input paths +in_trait_dir = "../DATA/GEO/Aniridia" +in_cohort_dir = "../DATA/GEO/Aniridia/GSE137997" + +# Output paths +out_data_file = "./output/preprocess/1/Aniridia/GSE137997.csv" +out_gene_data_file = "./output/preprocess/1/Aniridia/gene_data/GSE137997.csv" +out_clinical_data_file = "./output/preprocess/1/Aniridia/clinical_data/GSE137997.csv" +json_path = "./output/preprocess/1/Aniridia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Determine if gene expression data is available +is_gene_available = True # The title mentions "mRNA" alongside miRNA, so we consider gene expression data present. + +# 2. Identify rows for trait, age, and gender, and define their conversion functions + +# Based on the sample characteristics dictionary: +# 0 -> age data +# 1 -> gender data +# 2 -> "disease: AAK" or "disease: healthy control" +# This suggests: +trait_row = 2 +age_row = 0 +gender_row = 1 + +def convert_trait(value: str) -> int: + """ + Convert 'disease: AAK' or 'disease: healthy control' to binary (1 for aniridia, 0 for control). + Unknown or unexpected values become None. + """ + try: + val = value.split(':', 1)[1].strip().lower() + if 'aak' in val: + return 1 + elif 'healthy' in val: + return 0 + else: + return None + except: + return None + +def convert_age(value: str) -> float: + """ + Convert 'age: 20' etc. to a float (continuous). Unknown values become None. + """ + try: + val = value.split(':', 1)[1].strip() + return float(val) + except: + return None + +def convert_gender(value: str) -> int: + """ + Convert 'gender: F', 'gender: M', 'gender: W' to binary (female=0, male=1). + 'W' presumed female. Unknown or unexpected become None. + """ + try: + val = value.split(':', 1)[1].strip().lower() + if val in ['f', 'w', 'female', 'woman', 'women']: + return 0 + elif val in ['m', 'male']: + return 1 + else: + return None + except: + return None + +# 3. Conduct initial filtering and save metadata +is_trait_available = (trait_row is not None) +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical feature extraction if trait data is available +if trait_row is not None: + selected_clinical_df = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + # Preview + preview_result = preview_df(selected_clinical_df) + print("Preview of selected clinical features:", preview_result) + # Save clinical data + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These are microRNA identifiers (e.g. hsa-miR-1-3p) rather than standard human gene symbols; +# they do not require further mapping to gene symbols. +print("requires_gene_mapping = False") +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Aniridia/code/GSE204791.py b/p1/preprocess/Aniridia/code/GSE204791.py new file mode 100644 index 0000000000000000000000000000000000000000..f4b3ffde544084ba64e24a8ee36d6c22e4683f17 --- /dev/null +++ b/p1/preprocess/Aniridia/code/GSE204791.py @@ -0,0 +1,183 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Aniridia" +cohort = "GSE204791" + +# Input paths +in_trait_dir = "../DATA/GEO/Aniridia" +in_cohort_dir = "../DATA/GEO/Aniridia/GSE204791" + +# Output paths +out_data_file = "./output/preprocess/1/Aniridia/GSE204791.csv" +out_gene_data_file = "./output/preprocess/1/Aniridia/gene_data/GSE204791.csv" +out_clinical_data_file = "./output/preprocess/1/Aniridia/clinical_data/GSE204791.csv" +json_path = "./output/preprocess/1/Aniridia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # The series includes mRNA expression, so we consider it gene expression data. + +# 2. Variable Availability and Data Type Conversion +# 2.1 Determine row indices for 'trait', 'age', 'gender' +# Based on the sample characteristics dictionary: +# - 0: ['age: 59', 'age: 28', ... ] +# - 1: ['gender: F', 'gender: M'] +# - 2: ['disease: KC', 'disease: healthy control'] +# - 3: [ ... staging info ... ] +# We are looking for "Aniridia" but our dictionary lists "KC" or "healthy control" for disease. +# Hence, we do not have data for "Aniridia." So trait_row = None. + +trait_row = None # No data on "Aniridia" found +age_row = 0 # Multiple ages are present +gender_row = 1 # "F" and "M" are present + +# 2.2 Write conversion functions +def convert_trait(val: str): + """ + Attempt to parse 'Aniridia' or 'control' from the string after the colon. + Since 'Aniridia' is not actually in our sample data, return None. + """ + return None + +def convert_age(val: str): + """ + Parse the value after the colon and convert to float. + Non-numeric or invalid data is converted to None. + """ + parts = val.split(':') + if len(parts) < 2: + return None + raw_value = parts[1].strip() + try: + return float(raw_value) + except ValueError: + return None + +def convert_gender(val: str): + """ + Parse the value after the colon and convert: + F -> 0 + M -> 1 + Otherwise -> None + """ + parts = val.split(':') + if len(parts) < 2: + return None + raw_value = parts[1].strip().upper() + if raw_value == 'F': + return 0 + elif raw_value == 'M': + return 1 + else: + return None + +# 3. Save Metadata +# Trait data availability is determined by whether trait_row is None. +is_trait_available = (trait_row is not None) + +# Perform initial filtering (is_final=False). +# This will record metadata if data fails initial filtering. +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, clinical data extraction is skipped. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These identifiers appear to be microarray probe IDs or custom probe identifiers rather than standard human gene symbols. +# Therefore, they need to be mapped to gene symbols. + +requires_gene_mapping = True +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# Gene Identifier Mapping + +# 1. Identify which columns correspond to the expression data's probe ID and to the gene symbols. +# From the annotation preview, "ID" appears to match the probe identifiers (e.g., "A_19_P..."), +# and "GENE_SYMBOL" appears to be the gene symbol column. + +probe_id_col = "ID" +gene_symbol_col = "GENE_SYMBOL" + +# 2. Extract the mapping information between probe IDs and gene symbols. +gene_mapping_df = get_gene_mapping(gene_annotation, probe_id_col, gene_symbol_col) + +# 3. Apply the mapping to convert probe-level data into gene-level data. +gene_data = apply_gene_mapping(gene_data, gene_mapping_df) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# Since in previous steps we determined trait_row = None (no available trait data), +# we cannot link clinical data or perform trait-based filtering. Hence, we skip steps +# that depend on clinical or trait information. + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. No trait data found; skip clinical linking, missing-value handling, and bias assessment. +print("No trait data found. Skipping clinical linking, missing-value handling, and bias assessment.") + +# 3. Conduct final quality validation and save metadata. +# Since there's no trait data, we must pass some dummy DataFrame and a boolean for is_biased +# to avoid the ValueError in final mode. +dummy_df = pd.DataFrame() +is_biased_dummy = False # Arbitrary placeholder since we can't assess bias +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, + is_biased=is_biased_dummy, + df=dummy_df, + note="Trait data not found; dataset cannot be used for trait-based analysis." +) + +# 4. Because we don't have usable trait data, skip saving the linked data +if is_usable: + # This case should not occur since there's no trait data + pass +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Aniridia/code/TCGA.py b/p1/preprocess/Aniridia/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..a331fb1db23d9b49f821fc0cfbc4e63abbfa99e2 --- /dev/null +++ b/p1/preprocess/Aniridia/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Aniridia" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Aniridia/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Aniridia/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Aniridia/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Aniridia/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Aniridia/cohort_info.json b/p1/preprocess/Aniridia/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..dd8c357fbee78744a2b95975c53b274b94719e36 --- /dev/null +++ b/p1/preprocess/Aniridia/cohort_info.json @@ -0,0 +1 @@ +{"GSE204791": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data not found; dataset cannot be used for trait-based analysis."}, "GSE137997": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}, "GSE137996": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}} \ No newline at end of file diff --git a/p1/preprocess/Aniridia/gene_data/GSE137996.csv b/p1/preprocess/Aniridia/gene_data/GSE137996.csv new file mode 100644 index 0000000000000000000000000000000000000000..a0a285b0c4f43689162124d095eb547b629fd39e --- /dev/null +++ b/p1/preprocess/Aniridia/gene_data/GSE137996.csv @@ -0,0 +1 @@ +Gene,GSM4096389,GSM4096390,GSM4096391,GSM4096392,GSM4096393,GSM4096394,GSM4096395,GSM4096396,GSM4096397,GSM4096398,GSM4096399,GSM4096400,GSM4096401,GSM4096402,GSM4096403,GSM4096404,GSM4096405,GSM4096406,GSM4096407,GSM4096408,GSM4096409,GSM4096410,GSM4096411,GSM4096412,GSM4096413,GSM4096414,GSM4096415,GSM4096416,GSM4096417,GSM4096418,GSM4096419,GSM4096420,GSM4096421,GSM4096422,GSM4096423,GSM4096424,GSM4096425,GSM4096426,GSM4096427,GSM4096428 diff --git a/p1/preprocess/Aniridia/gene_data/GSE137997.csv b/p1/preprocess/Aniridia/gene_data/GSE137997.csv new file mode 100644 index 0000000000000000000000000000000000000000..09030fa447c743c5ac4332599513ae15a8dbf101 --- /dev/null +++ b/p1/preprocess/Aniridia/gene_data/GSE137997.csv @@ -0,0 +1 @@ +ID,GSM4096349,GSM4096350,GSM4096351,GSM4096352,GSM4096353,GSM4096354,GSM4096355,GSM4096356,GSM4096357,GSM4096358,GSM4096359,GSM4096360,GSM4096361,GSM4096362,GSM4096363,GSM4096364,GSM4096365,GSM4096366,GSM4096367,GSM4096368,GSM4096369,GSM4096370,GSM4096371,GSM4096372,GSM4096373,GSM4096374,GSM4096375,GSM4096376,GSM4096377,GSM4096378,GSM4096379,GSM4096380,GSM4096381,GSM4096382,GSM4096383,GSM4096384,GSM4096385,GSM4096386,GSM4096387,GSM4096388 diff --git a/p1/preprocess/Aniridia/gene_data/GSE204791.csv b/p1/preprocess/Aniridia/gene_data/GSE204791.csv new file mode 100644 index 0000000000000000000000000000000000000000..80ddbb979251abb1c29c476ada6b903eb887b534 --- /dev/null +++ b/p1/preprocess/Aniridia/gene_data/GSE204791.csv @@ -0,0 +1 @@ +Gene,GSM6193900,GSM6193903,GSM6193906,GSM6193908,GSM6193911,GSM6193913,GSM6193916,GSM6193918,GSM6193920,GSM6193923,GSM6193925,GSM6193928,GSM6193930,GSM6193933,GSM6193935,GSM6193938,GSM6193940,GSM6193943,GSM6193945,GSM6193948,GSM6193950,GSM6193953,GSM6193955,GSM6193957,GSM6193960,GSM6193962,GSM6193965,GSM6193967,GSM6193970,GSM6193972,GSM6193975 diff --git a/p1/preprocess/Ankylosing_Spondylitis/clinical_data/GSE25101.csv b/p1/preprocess/Ankylosing_Spondylitis/clinical_data/GSE25101.csv new file mode 100644 index 0000000000000000000000000000000000000000..db3afda255818dc3dfb78dc1f01f50f0c7b2cdec --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/clinical_data/GSE25101.csv @@ -0,0 +1,2 @@ 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a/p1/preprocess/Ankylosing_Spondylitis/code/GSE25101.py b/p1/preprocess/Ankylosing_Spondylitis/code/GSE25101.py new file mode 100644 index 0000000000000000000000000000000000000000..2de81b75bcb63afd716ec45279cba33d3e42cb97 --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/code/GSE25101.py @@ -0,0 +1,191 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Ankylosing_Spondylitis" +cohort = "GSE25101" + +# Input paths +in_trait_dir = "../DATA/GEO/Ankylosing_Spondylitis" +in_cohort_dir = "../DATA/GEO/Ankylosing_Spondylitis/GSE25101" + +# Output paths +out_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/GSE25101.csv" +out_gene_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/gene_data/GSE25101.csv" +out_clinical_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/clinical_data/GSE25101.csv" +json_path = "./output/preprocess/1/Ankylosing_Spondylitis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1) Gene Expression Data Availability +# Based on the series description, this dataset uses "Illumina HT-12 Whole-Genome Expression BeadChips". +# Hence, we conclude that it likely contains gene expression data. +is_gene_available = True + +# 2) Variable Availability and Data Type Conversion + +# Inspecting the sample characteristics dictionary: +# {0: ['tissue: Whole blood'], +# 1: ['cell type: PBMC'], +# 2: ['disease status: Ankylosing spondylitis patient', 'disease status: Normal control']} + +# -- Trait -- +# The data for "Ankylosing_Spondylitis" can be inferred from key=2 (it has at least 2 unique values). +trait_row = 2 + +# -- Age -- +# No age information is found. So: +age_row = None + +# -- Gender -- +# No gender information is found. So: +gender_row = None + +# Data type choices: +# Since the "trait" variable has two categories (patient vs control), we treat it as binary. +# For "age" and "gender", no data is available, so we won't convert. + +def convert_trait(value: str): + """ + Convert disease status to binary: + 'Ankylosing spondylitis patient' -> 1 + 'Normal control' -> 0 + Unknown -> None + """ + # Split by ':', then take the part after the colon if present + parts = value.split(':', 1) + val = parts[1].strip().lower() if len(parts) > 1 else parts[0].strip().lower() + + if 'ankylosing spondylitis patient' in val: + return 1 + elif 'normal control' in val: + return 0 + else: + return None + +def convert_age(value: str): + # Age not available in this dataset, so all become None + return None + +def convert_gender(value: str): + # Gender not available in this dataset, so all become None + return None + +# 3) Save Metadata with initial filtering +# Trait data is available if trait_row is not None +is_trait_available = (trait_row is not None) + +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4) Clinical Feature Extraction (only if trait_row is not None) +if trait_row is not None: + selected_clinical = geo_select_clinical_features( + clinical_df=clinical_data, # assume 'clinical_data' was loaded in a previous step + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + # Preview the extracted clinical features + print("Preview of selected clinical features:") + print(preview_df(selected_clinical, n=5)) + + # Save the clinical data + selected_clinical.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These ILMN_* identifiers are Illumina probe IDs, not standard human gene symbols. +# Therefore, they require mapping to gene symbols. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1) Identify the columns in gene_annotation that match gene_data's "ID" and the gene symbol +# From inspection, "ID" corresponds to the Illumina probe IDs in gene_data, and "Symbol" contains the gene symbols. + +# 2) Create the gene mapping dataframe using probe IDs and gene symbols +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Symbol') + +# 3) Convert probe-level to gene-level data using the mapping +gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df) + +# Print out some information about the mapped gene data +print("Gene expression data after mapping:") +print("Shape of gene_data:", gene_data.shape) +print("First 20 mapped gene symbols:", list(gene_data.index[:20])) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Ankylosing_Spondylitis/code/GSE73754.py b/p1/preprocess/Ankylosing_Spondylitis/code/GSE73754.py new file mode 100644 index 0000000000000000000000000000000000000000..bd9a13954a0f62baed75820a49f9c0a5605ecb58 --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/code/GSE73754.py @@ -0,0 +1,183 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Ankylosing_Spondylitis" +cohort = "GSE73754" + +# Input paths +in_trait_dir = "../DATA/GEO/Ankylosing_Spondylitis" +in_cohort_dir = "../DATA/GEO/Ankylosing_Spondylitis/GSE73754" + +# Output paths +out_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/GSE73754.csv" +out_gene_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/gene_data/GSE73754.csv" +out_clinical_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/clinical_data/GSE73754.csv" +json_path = "./output/preprocess/1/Ankylosing_Spondylitis/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# Step 1. Determine gene expression data availability +is_gene_available = True # Based on the background (differential gene expression analysis), we consider this dataset to have gene data + +# Step 2. Identify data availability for trait, age, and gender +# According to the sample characteristics dictionary: +# 0 -> 'Sex: Male', 'Sex: Female' +# 1 -> 'age (yr): 53', ... +# 3 -> 'disease: Ankylosing Spondylitis', 'disease: healthy control' +trait_row = 3 +age_row = 1 +gender_row = 0 + +# Step 2.2 Define conversion functions +def convert_trait(x: str): + # e.g., "disease: Ankylosing Spondylitis" -> 1, "disease: healthy control" -> 0 + # parse out the value after the colon + try: + val = x.split(":", 1)[1].strip().lower() + except IndexError: + return None + if "ankylosing spondylitis" in val: + return 1 + elif "healthy control" in val: + return 0 + else: + return None + +def convert_age(x: str): + # e.g., "age (yr): 53" -> 53 + try: + val = x.split(":", 1)[1].strip() + return float(val) + except: + return None + +def convert_gender(x: str): + # e.g., "Sex: Male" -> 1, "Sex: Female" -> 0 + try: + val = x.split(":", 1)[1].strip().lower() + except IndexError: + return None + if "male" in val: + return 1 + elif "female" in val: + return 0 + else: + return None + +# Step 3. Initial filtering and save metadata +is_trait_available = (trait_row is not None) +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# Step 4. Clinical feature extraction (only if trait_row is not None) +if trait_row is not None: + # 'clinical_data' is assumed to be the DataFrame previously obtained for sample characteristics + selected_clinical_df = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + + # Preview the result + print("Preview of clinical features:") + print(preview_df(selected_clinical_df, n=5)) + + # Save to CSV + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# The observed gene identifiers (ILMN_####) are Illumina microarray probe IDs. +# They are not standard human gene symbols and require mapping to official gene symbols. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify the annotation columns for mapping +# - The gene expression data uses 'ILMN_####' as identifiers, which match the 'ID' column in the annotation. +# - The gene symbols are in the 'Symbol' column. + +# 2. Extract the gene mapping dataframe using the library function +gene_mapping_df = get_gene_mapping(annotation=gene_annotation, prob_col='ID', gene_col='Symbol') + +# 3. Convert probe-level measurements to gene expression data +gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=gene_mapping_df) + +# Print shape of the new gene_data to confirm processing +print("Gene data shape after mapping:", gene_data.shape) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Ankylosing_Spondylitis/code/TCGA.py b/p1/preprocess/Ankylosing_Spondylitis/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..060f71a9b25d0be2540fea006049cf7e13de3b9b --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Ankylosing_Spondylitis" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Ankylosing_Spondylitis/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Ankylosing_Spondylitis/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Ankylosing_Spondylitis/cohort_info.json b/p1/preprocess/Ankylosing_Spondylitis/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..02c8027cb39fca82c6313a429dfa5b304456d927 --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/cohort_info.json @@ -0,0 +1 @@ +{"GSE73754": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}, "GSE25101": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}} \ No newline at end of file diff --git a/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE25101.csv b/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE25101.csv new file mode 100644 index 0000000000000000000000000000000000000000..09b1c62ceb23cb202ac437fcffe2fd6100862cbb --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE25101.csv @@ -0,0 +1 @@ +Gene,GSM616668,GSM616669,GSM616670,GSM616671,GSM616672,GSM616673,GSM616674,GSM616675,GSM616676,GSM616677,GSM616678,GSM616679,GSM616680,GSM616681,GSM616682,GSM616683,GSM616684,GSM616685,GSM616686,GSM616687,GSM616688,GSM616689,GSM616690,GSM616691,GSM616692,GSM616693,GSM616694,GSM616695,GSM616696,GSM616697,GSM616698,GSM616699 diff --git a/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE73754.csv b/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE73754.csv new file mode 100644 index 0000000000000000000000000000000000000000..25ba45514b81143404d96795bf6707ccefa835e7 --- /dev/null +++ b/p1/preprocess/Ankylosing_Spondylitis/gene_data/GSE73754.csv @@ -0,0 +1 @@ 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0000000000000000000000000000000000000000..55bffa1740139754242c196cddfe7c51fc393c61 --- /dev/null +++ b/p1/preprocess/Anorexia_Nervosa/clinical_data/GSE60190.csv @@ -0,0 +1,4 @@ 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+in_trait_dir = "../DATA/GEO/Anorexia_Nervosa" +in_cohort_dir = "../DATA/GEO/Anorexia_Nervosa/GSE60190" + +# Output paths +out_data_file = "./output/preprocess/1/Anorexia_Nervosa/GSE60190.csv" +out_gene_data_file = "./output/preprocess/1/Anorexia_Nervosa/gene_data/GSE60190.csv" +out_clinical_data_file = "./output/preprocess/1/Anorexia_Nervosa/clinical_data/GSE60190.csv" +json_path = "./output/preprocess/1/Anorexia_Nervosa/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Determine if gene expression data is available +# Based on the background info (Illumina HumanHT-12 v3 microarray measurements), +# we conclude that gene expression data is available. +is_gene_available = True + +# 2. Identify rows and define conversion functions for trait, age, and gender. + +# After examining the sample characteristics dictionary, we select: +# - trait information in row 3 ("dx: ED", "dx: OCD", "dx: Control", etc.) +# We'll map "dx: ED" -> 1 (our trait of interest, albeit grouped as ED) +# and everything else -> 0. +trait_row = 3 + +# - age information in row 5 (e.g., "age: 50.421917") +age_row = 5 + +# - gender information in row 7 (e.g., "Sex: F" or "Sex: M") +gender_row = 7 + +def convert_trait(x: str) -> Optional[int]: + parts = x.split(":", 1) + if len(parts) < 2: + return None + val = parts[1].strip() + # Convert "ED" to 1, others (including OCD, Control, etc.) to 0 + return 1 if val == "ED" else 0 + +def convert_age(x: str) -> Optional[float]: + parts = x.split(":", 1) + if len(parts) < 2: + return None + val = parts[1].strip() + try: + return float(val) + except ValueError: + return None + +def convert_gender(x: str) -> Optional[int]: + parts = x.split(":", 1) + if len(parts) < 2: + return None + val = parts[1].strip() + # Map "F" -> 0, "M" -> 1 + if val == "F": + return 0 + elif val == "M": + return 1 + return None + +# 2.1 Check if trait data is available +# We consider trait data available if trait_row is not None +is_trait_available = (trait_row is not None) + +# 3. Perform initial filtering and save metadata +# (is_final=False for initial filtering) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. If trait_row is not None, extract clinical features, preview, and save +if trait_row is not None: + clinical_data_selected = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + # Preview the selected clinical data + preview = preview_df(clinical_data_selected) + print("Preview of selected clinical features:", preview) + + # Save the clinical features to CSV + clinical_data_selected.to_csv(out_clinical_data_file) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +print("These are Illumina probe identifiers (e.g., ILMN_xxxx), which are not human gene symbols and thus require mapping.") +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP6 - Gene Identifier Mapping + +# 1. Identify the columns for probe IDs and gene symbols in the gene_annotation DataFrame. +# From observing the data preview, "ID" holds Illumina probe identifiers matching our gene_data index, +# and "Symbol" holds the gene symbol information. +mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Symbol") + +# 2. Apply this mapping to the probe-level expression data to get gene-level expression data. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# Now, 'gene_data' contains gene expression values indexed by gene symbols. +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Make sure we have the clinical data in scope. +# In previous steps, we stored it as 'clinical_data_selected', so define 'selected_clinical' for consistency here. +selected_clinical = clinical_data_selected + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, # We do have a trait column + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anorexia_Nervosa/code/TCGA.py b/p1/preprocess/Anorexia_Nervosa/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..ad35832cae56100ad92c902a1099e9a0181983b1 --- /dev/null +++ b/p1/preprocess/Anorexia_Nervosa/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anorexia_Nervosa" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Anorexia_Nervosa/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Anorexia_Nervosa/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Anorexia_Nervosa/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Anorexia_Nervosa/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Anorexia_Nervosa/cohort_info.json b/p1/preprocess/Anorexia_Nervosa/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..c90a784467c3145a4473ce1afd1d8b70bb31d9ce --- /dev/null +++ b/p1/preprocess/Anorexia_Nervosa/cohort_info.json @@ -0,0 +1 @@ +{"GSE60190": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}} \ No newline at end of file diff --git a/p1/preprocess/Anorexia_Nervosa/gene_data/GSE60190.csv b/p1/preprocess/Anorexia_Nervosa/gene_data/GSE60190.csv new file mode 100644 index 0000000000000000000000000000000000000000..0ad04b0f87a53bc4ecf7fa48871fccbb8837b3ec --- /dev/null +++ b/p1/preprocess/Anorexia_Nervosa/gene_data/GSE60190.csv @@ 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+in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE119995" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE119995.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE119995.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE119995.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # Based on the description: "Exposure-induced changes of plasma mRNA expression levels." + +# 2. Variable Availability and Data Type Conversion +# The sample characteristics dictionary is: +# {0: ['disease: panic disorder'], +# 1: ['tissue: blood plasma'], +# 2: ['Sex: female', 'Sex: male', 'Sex: not determined'], +# 3: ['medication: 0', 'medication: 1'], +# 4: ['timepoint: b1', 'timepoint: p24_1', 'timepoint: pe1'], +# 5: [ ... 'individual: #' ... ]} +# +# We see no row for a varying 'trait' or 'age' field, but row 2 has 'Sex' with different values. +trait_row = None # No row with 'trait' variation (only "disease: panic disorder"). +age_row = None # No age data found in the dictionary. +gender_row = 2 # Row with varying "Sex" values. + +def convert_trait(x: str): + return None # Trait is not available in this dataset for variation. + +def convert_age(x: str): + return None # Age is not available. + +def convert_gender(x: str): + # Example: "Sex: female" -> 'female' + val = x.split(':')[-1].strip().lower() + if val == 'female': + return 0 + elif val == 'male': + return 1 + else: + return None + +# 3. Save Metadata (initial filtering) +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Skip because trait_row is None. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Since the identifiers follow the pattern "ILMN_", they appear to be Illumina probe IDs rather than human gene symbols. +# Therefore, they require mapping to gene symbols. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Determine the appropriate columns for the probe IDs and gene symbols +prob_col = 'ID' # Matches the "ILMN_xxxxx" identifiers seen in the gene expression data +gene_col = 'Symbol' # Column containing gene symbols + +# 2. Extract the gene mapping from the annotation dataframe +mapping_df = get_gene_mapping(gene_annotation, prob_col, gene_col) + +# 3. Convert probe-level measurements to gene-level by applying the mapping +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1) Normalize the gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Because 'trait_row' was None in earlier steps, we have no varying trait data. Therefore, we cannot link +# clinical and genetic data in a meaningful way (no trait to analyze) nor perform trait-based processing. + +# 2) As we are in the final step and must call 'validate_and_save_cohort_info' with is_final=True, we need +# to provide both 'df' and 'is_biased'. Since there's no trait data, we create an empty DataFrame and +# set is_biased=False (the trait is effectively unavailable, so "bias" is moot). + +empty_df = pd.DataFrame() + +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, # We do have gene expression data + is_trait_available=False, # No valid trait data + is_biased=False, # Arbitrary boolean because we must supply one; trait isn't actually present + df=empty_df, + note="Trait data not available; skipping linking and final dataset output." +) + +# 3) If the dataset were usable, we'd save a final linked dataset, but it's not usable without a trait. +if is_usable: + # This block won't run because is_trait_available=False => is_usable=False + pass +else: + print("No trait data found; the dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE60190.py b/p1/preprocess/Anxiety_disorder/code/GSE60190.py new file mode 100644 index 0000000000000000000000000000000000000000..b66eb2a546e7dd4dc19a56c14b71ce71754574a5 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE60190.py @@ -0,0 +1,174 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE60190" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE60190" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE60190.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE60190.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE60190.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# Step 1: Determine if this dataset likely contains gene expression data +# From the background info, it's clear that this is a microarray-based gene expression dataset. +is_gene_available = True + +# Step 2: Identify data availability for trait, age, and gender +# and define the corresponding row indices and conversion functions. +# --------------------------------------------------------------- +# 2.1 Data Availability +# We do not see any explicit or strongly inferable row key for "Anxiety_disorder" in the sample characteristics, +# so we consider the trait unavailable. +trait_row = None + +# We see age data in key=5 with multiple unique numeric values, so it's available. +age_row = 5 + +# We see gender data in key=7 ("Sex: F" or "Sex: M"), so it's available. +gender_row = 7 + +# 2.2 Data Type Conversion +def convert_trait(x: str): + """ + Since trait_row is None (trait not available), this function is not actually used. + We provide a placeholder that returns None. + """ + return None + +def convert_age(x: str): + """ + Convert age from a string like 'age: 30.5' to a float. + Unknown or invalid values become None. + """ + try: + # Split at colon, take right side, strip spaces + val_str = x.split(':', 1)[1].strip() + return float(val_str) + except: + return None + +def convert_gender(x: str): + """ + Convert gender from a string like 'Sex: F' or 'Sex: M' to 0 or 1. + Unknown values become None. + """ + try: + val_str = x.split(':', 1)[1].strip().upper() + if val_str in ['F', 'FEMALE']: + return 0 + elif val_str in ['M', 'MALE']: + return 1 + else: + return None + except: + return None + +# Step 3: Conduct initial filtering on dataset usability +# Trait data availability depends on whether trait_row is None. +is_trait_available = (trait_row is not None) + +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# Step 4: Clinical Feature Extraction +# Only do this step if trait_row is not None. In this case, trait_row is None, so we skip it. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# After examining the provided gene identifiers, they are Illumina probe IDs (e.g., ILMN_1343291), +# which are not standard human gene symbols. Therefore, they require mapping to the correct gene symbols. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Decide which column in the gene annotation stores the probe IDs matching those in the gene expression data ("ID"), +# and which column stores the gene symbols ("Symbol"). +probe_id_col = "ID" +gene_symbol_col = "Symbol" + +# 2. Get a gene mapping dataframe by extracting these two columns. +gene_mapping_df = get_gene_mapping( + annotation=gene_annotation, + prob_col=probe_id_col, + gene_col=gene_symbol_col +) + +# 3. Convert probe-level measurements to gene-level measurements by applying the mapping. +gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=gene_mapping_df) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Since trait_row was None, we have no trait data; skip linking clinical data or trait-based steps. + +# 5. Conduct final quality validation +# The library mandates that when is_final=True, we must provide both df and is_biased as non-None. +# Here, we have no trait data, so we pass an empty DataFrame and set is_biased=False (arbitrary boolean), +# which will mark the dataset as not usable for trait-based analysis. +empty_df = pd.DataFrame() +is_trait_available = False +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, # We did confirm gene expression is available + is_trait_available=is_trait_available, + is_biased=False, # Arbitrary boolean to satisfy the function requirement + df=empty_df, + note="Trait data is unavailable for this cohort." +) + +# 6. If the dataset were usable, we would save final linked data, but here it will not be usable. +if is_usable: + print("Dataset unexpectedly marked as usable; no trait present.") +else: + print("No trait data, so the dataset is not usable for trait-based analysis. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE60491.py b/p1/preprocess/Anxiety_disorder/code/GSE60491.py new file mode 100644 index 0000000000000000000000000000000000000000..b588b38d9aac5e51a2b213fe44e781432a4ff410 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE60491.py @@ -0,0 +1,148 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE60491" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE60491" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE60491.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE60491.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE60491.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # The series explicitly mentions "gene expression profiling", so we consider it available. + +# 2. Variable Availability and Data Type Conversion +# After examining the sample characteristics, +# we do not see any key referencing "anxiety" or "anxiety_disorder." +# Therefore, we conclude that the trait data is not available in this dataset. +trait_row = None + +# The 'age' information appears in row 0. +age_row = 0 + +# The 'gender' information appears in row 1 (it's labeled 'male: 0' or 'male: 1'). +gender_row = 1 + +# Define data-type conversion functions. +def convert_trait(value: str): + # Trait data is unavailable, so this function won't be used. + # We'll just return None as a placeholder. + return None + +def convert_age(value: str): + # Extract the numeric part after the colon. Convert to float if possible, else None. + try: + val = value.split(':', 1)[1].strip() + return float(val) + except: + return None + +def convert_gender(value: str): + # The field is "male: 0" for female, "male: 1" for male. + # We'll parse it and convert to 0 (female) or 1 (male). + try: + val = value.split(':', 1)[1].strip() + return 1 if val == '1' else 0 + except: + return None + +# Determine whether trait data is available +is_trait_available = trait_row is not None + +# 3. Save Metadata (initial filtering) +_ = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, we skip this step. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the identifiers such as "7A5" (likely SLC7A5) and "A2BP1" (also known as RBFOX1), +# it appears that these gene symbols are not standardized. Therefore, mapping is required. +requires_gene_mapping = True +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify which columns match the gene expression data +# Based on the previous previews, 'ID' matches the expression data identifiers, +# and 'ORF' contains the gene symbols. + +mapping_df = get_gene_mapping(annotation=gene_annotation, prob_col='ID', gene_col='ORF') + +# 2. Convert probe-level measurements to gene expression data by applying the gene mapping +gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df) + +# Print a small preview of the resulting mapped gene data +print("Mapped gene data shape:", gene_data.shape) +print("First 5 mapped gene symbols:", gene_data.index[:5]) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(clinical_data, normalized_gene_data) + +# Since trait_row is None, trait data is unavailable, we cannot perform final trait-based validation. + +# 3. We skip any trait-based missing value handling and bias checking because there's no trait. + +# 4. Perform only partial metadata validation (is_final=False) since no trait data is available. +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False +) + +# 5. We do not save a final linked data file because trait-based analysis is not possible. +print("Dataset does not have the specified trait data; no final data output generated.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE61672.py b/p1/preprocess/Anxiety_disorder/code/GSE61672.py new file mode 100644 index 0000000000000000000000000000000000000000..a55f3950dffae135b7daeb7973b521c31ae73493 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE61672.py @@ -0,0 +1,332 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE61672" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE61672" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE61672.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE61672.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE61672.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +import pandas as pd +import os +import json +from typing import Optional, Callable + +# The sample characteristics dictionary from the previous step: +sample_dict = { + 0: ['age: 44', 'age: 59', 'age: 39', 'age: 64', 'age: 58', 'age: 45', 'age: 37', 'age: 40', + 'age: 57', 'age: 52', 'age: 62', 'age: 55', 'age: 53', 'age: 47', 'age: 48', 'age: 49', + 'age: 35', 'age: 46', 'age: 54', 'age: 67', 'age: 51', 'age: 34', 'age: 60', 'age: 41', + 'age: 38', 'age: 73', 'age: 28', 'age: 56', 'age: 71', 'age: 50'], + 1: ['Sex: F', 'Sex: M', 'body mass index: 25.1', 'body mass index: 31.1', 'body mass index: 29.4', + 'body mass index: 27.6', 'body mass index: 24.6', 'body mass index: 28', 'body mass index: 33.9', + 'body mass index: 35', 'body mass index: 18.1', 'body mass index: 19.2', 'body mass index: 39.2', + 'body mass index: 26.8', 'body mass index: 21.3', 'body mass index: 36.5', 'body mass index: 19.5', + 'body mass index: 24.4', 'body mass index: 26.4', 'body mass index: 26.2', 'body mass index: 23.8', + 'body mass index: 19.7', 'body mass index: 30.6', 'body mass index: 22.8', 'body mass index: 22.1', + 'body mass index: 33.4', 'body mass index: 26.6', 'body mass index: 21.8', 'body mass index: 24.3', + 'body mass index: 27'], + 2: ['body mass index: 22.2', 'body mass index: 33.1', 'body mass index: 22.4', 'body mass index: 20.6', + 'body mass index: 27.5', 'body mass index: 21.9', 'body mass index: 26.1', 'body mass index: 34.8', + 'body mass index: 20.8', 'body mass index: 23.3', 'body mass index: 22.7', 'body mass index: 26.4', + 'body mass index: 32.5', 'body mass index: 21.6', 'body mass index: 27.6', 'body mass index: 25.7', + 'body mass index: 33.3', 'body mass index: 31.6', 'body mass index: 28', 'body mass index: 41.1', + 'body mass index: 19.7', 'body mass index: 22.1', 'body mass index: 20.7', 'body mass index: 30.9', + 'body mass index: 17.8', 'body mass index: 22.5', 'body mass index: 40.6', 'body mass index: 28.9', + 'body mass index: 26', 'body mass index: 22'], + 3: ['ethnicity: CAU', 'ethnicity: AFR', 'ethnicity: ASN', 'ethnicity: AMI', 'ethnicity: CAH', + 'gad7 score: 6', 'gad7 score: 1', 'gad7 score: 0', 'gad7 score: 2', 'gad7 score: 3', 'gad7 score: 5', + 'gad7 score: 4', 'gad7 score: 9', 'gad7 score: 7', 'gad7 score: 8', 'hybridization batch: C', + 'gad7 score: .', 'gad7 score: 16', 'gad7 score: 12', 'gad7 score: 11', 'gad7 score: 21', + 'gad7 score: 18', 'gad7 score: 14'], + 4: ['gad7 score: 2', 'gad7 score: 0', 'gad7 score: 3', 'gad7 score: 7', 'gad7 score: 4', + 'gad7 score: 9', 'gad7 score: 1', 'gad7 score: 10', 'gad7 score: 5', 'gad7 score: 17', 'gad7 score: 6', + 'gad7 score: 8', 'gad7 score: 12', 'gad7 score: 11', 'gad7 score: 14', 'gad7 score: .', + 'hybridization batch: Z', 'gad7 score: 18', 'hybridization batch: O', 'gad7 score: 13', + 'gad7 score: 15', 'gad7 score: 20', 'gad7 score: 21', 'gad7 score: 19', 'anxiety case/control: case', + 'anxiety case/control: control', 'hybridization batch: B', None, 'hybridization batch: C', + 'hybridization batch: D'], + 5: ['hybridization batch: Z', 'anxiety case/control: control', 'anxiety case/control: case', + 'rin: 8.4', 'hybridization batch: A', 'hybridization batch: O', 'rin: 6', None, + 'hybridization batch: B', 'rin: 9.5', 'rin: 9.1', 'rin: 9.3', 'rin: 9.7', 'rin: 9.6', + 'rin: 8.7', 'hybridization batch: C', 'rin: 8.6', 'rin: 7.9', 'rin: 7.3', 'rin: 7.1', + 'rin: 8.9', 'rin: 9.8', 'rin: 9.4', 'rin: 9.2', 'rin: 8.8', 'rin: 10', 'rin: 9', 'rin: 9.9', + 'hybridization batch: D'], + 6: ['rin: 8.1', 'hybridization batch: Z', 'rin: 7.9', 'rin: 6.6', 'rin: 7.3', 'rin: 6.9', + 'rin: 6.8', 'rin: 7.5', 'rin: 6.7', 'rin: 6.5', 'rin: 7.8', 'rin: 7.6', 'rin: 8', 'rin: 7.4', + 'rin: 8.4', 'rin: 8.7', 'rin: 8.8', 'rin: 7.7', 'rin: 8.3', 'rin: 7', 'rin: 9', 'rin: 9.3', + 'rin: 8.9', None, 'rin: 8.2', 'rin: 9.2', 'rin: 7.2', 'rin: 7.1', 'hybridization batch: A', + 'rin: 9.8'], + 7: [None, 'rin: 7.8', 'rin: 8.1', 'rin: 6.6', 'rin: 6.5', 'rin: 6.7', 'rin: 7.2', 'rin: 7.7', + 'rin: 7.1', 'rin: 7', 'rin: 7.3', 'rin: 7.5', 'rin: 7.9', 'rin: 8.2', 'rin: 7.4', 'rin: 7.6', + 'rin: 6.8', 'rin: 9.4', 'rin: 8.6', 'rin: 8.3', 'rin: 8.8', 'rin: 8', 'rin: 8.4', 'rin: 8.7', + 'rin: 9', 'rin: 9.1', 'rin: 9.2', 'rin: 9.3', 'rin: 8.5', 'rin: 6.9'] +} + +# Construct the DataFrame where each row in sample_dict is a row in the DataFrame. +clinical_data = pd.DataFrame.from_dict(sample_dict, orient='index') + +# 1. Gene Expression Data Availability +# The background info specifies "genome-wide differential gene expression", +# so we set is_gene_available to True. +is_gene_available = True + +# 2. Variable Availability and Data Type Conversion +# Identify row keys for the variables (trait, age, gender) if they exist and are not constant. +# - Age is row 0, multiple distinct values => available. +age_row = 0 + +# - Trait (anxiety case/control) is found in row 4: "anxiety case/control: case"/"control" +trait_row = 4 + +# - Gender is in row 1: "Sex: F"/"Sex: M" along with BMI. Let's parse those "Sex" entries. +gender_row = 1 + +def convert_trait(value: str) -> Optional[int]: + """ + Convert values referring to 'anxiety case/control': + 'case' -> 1 + 'control' -> 0 + Everything else -> None + """ + parts = value.split(":", 1) + if len(parts) == 2: + header = parts[0].strip().lower() + val = parts[1].strip().lower() + if header == "anxiety case/control": + if val == "case": + return 1 + elif val == "control": + return 0 + return None + +def convert_age(value: str) -> Optional[float]: + """ + Convert values of the form 'age: 44' -> 44.0 + Otherwise -> None + """ + parts = value.split(":", 1) + if len(parts) == 2: + header = parts[0].strip().lower() + val = parts[1].strip() + if header == "age": + try: + return float(val) + except ValueError: + return None + return None + +def convert_gender(value: str) -> Optional[int]: + """ + For gender, convert: + 'Sex: F' -> 0 + 'Sex: M' -> 1 + Otherwise -> None + """ + parts = value.split(":", 1) + if len(parts) == 2: + header = parts[0].strip().lower() + val = parts[1].strip().lower() + if header == "sex": + if val == "f": + return 0 + elif val == "m": + return 1 + return None + +# 2.1 Check trait availability: +is_trait_available = (trait_row is not None) + +# 3. Save Metadata (initial filtering) +from tools.preprocess import validate_and_save_cohort_info, geo_select_clinical_features, preview_df + +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction if trait_row is not None +if trait_row is not None: + selected_clinical_df = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + preview = preview_df(selected_clinical_df) + print("Clinical dataframe preview:", preview) + + # Save the extracted clinical features + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +import re + +# 1. Gene Expression Data Availability +is_gene_available = True + +# 2. Variable Availability and Data Type Conversion +# (We do not see any evidence of actual row keys for trait, age, or gender, so set them to None.) +trait_row = None +age_row = None +gender_row = None + +# Define conversion functions even if rows are None, for consistency and future use. + +def convert_trait(val_str: str): + """Convert trait value to binary (0 for control, 1 for anxiety), None if unknown.""" + if val_str is None: + return None + # If there's a colon, separate out the last segment. + parts = val_str.split(":") + val_str = parts[-1].strip() if len(parts) > 1 else val_str.strip() + val_lower = val_str.lower() + if "anxiety" in val_lower: + return 1 + elif "control" in val_lower: + return 0 + return None + +def convert_age(val_str: str): + """Convert age to a continuous number, None if parsing fails.""" + if val_str is None: + return None + # If there's a colon, separate out the last segment. + parts = val_str.split(":") + val_str = parts[-1].strip() if len(parts) > 1 else val_str.strip() + # Extract numeric part from the string + match = re.search(r"(\d+(\.\d+)?)", val_str) + if match: + try: + return float(match.group(1)) + except ValueError: + return None + return None + +def convert_gender(val_str: str): + """Convert gender to binary (0 for female, 1 for male), None if unknown.""" + if val_str is None: + return None + # If there's a colon, separate out the last segment. + parts = val_str.split(":") + val_str = parts[-1].strip() if len(parts) > 1 else val_str.strip() + val_lower = val_str.lower() + if "female" in val_lower: + return 0 + elif "male" in val_lower: + return 1 + return None + +# Determine availability of trait data +is_trait_available = (trait_row is not None) + +# 3. Save Metadata - initial filtering +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, we skip the clinical feature extraction step. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These gene identifiers are from the Illumina platform (e.g., "ILMN_1343291"), not standard human gene symbols. +# Therefore, gene mapping to standard symbols is likely required. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. We observed that in the gene annotation dataframe, the column "ID" stores the same probe identifiers +# (e.g., ILMN_1343291) as in the gene expression data index, and the column "Symbol" stores the potential gene symbols. + +# 2. Get a gene mapping from 'ID' to 'Symbol'. +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Symbol') + +# 3. Convert probe-level measurements to gene expression data using our mapping. +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 8: Data Normalization and (Potential) Linking + +# Because, in earlier steps, we determined trait_row = None, the trait data is unavailable, +# so there's no clinical CSV file to read back in. By the instructions, we still finalize +# the process but skip linking and trait-based analysis. + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Since trait data is not available, we cannot link or run trait-based analyses. +print("Trait is not available (trait_row = None). Skipping linking and missing-value handling steps.") + +# 3. Perform final validation indicating that trait data is missing, causing the dataset to be unusable: +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, # Gene data exists + is_trait_available=False, # Trait data is not available + is_biased=None, # This must be None if is_trait_available=False + df=pd.DataFrame(), # Pass an empty DataFrame since we have no clinical+trait data + note="No trait data available, thus not usable for trait-based analysis." +) + +# 4. If the dataset is somehow deemed usable (unlikely, because no trait), save the final data anyway; +# otherwise skip saving. +if is_usable: + # This scenario won't occur, but included for completeness + out_data_file_placeholder = out_data_file.replace(".csv", "_linked_placeholder.csv") + pd.DataFrame().to_csv(out_data_file_placeholder, index=False) + print(f"Saved a placeholder linked dataset to {out_data_file_placeholder}") +else: + print("The dataset is not usable for trait-based association. Skipping final output of linked data.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE68526.py b/p1/preprocess/Anxiety_disorder/code/GSE68526.py new file mode 100644 index 0000000000000000000000000000000000000000..a793fb7a5b923e49a2940641ac61119c40d4e593 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE68526.py @@ -0,0 +1,201 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE68526" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE68526" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE68526.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE68526.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE68526.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Determine if gene expression data is available +is_gene_available = True # Based on the background info: "Gene expression profiling was carried out ..." +# 2. Determine availability of trait, age, gender, and define conversion functions + +# From the dictionary, anxiety is at row 13 and has multiple distinct values. +trait_row = 13 + +# Age is at row 0, with multiple distinct values. +age_row = 0 + +# Gender is at row 1, with two distinct values (female: 0 or 1). +gender_row = 1 + +# Data type conversions: +def convert_trait(value: str): + """ + Convert the anxiety string value after colon to a float (continuous measure). + Returns None if 'missing' or conversion fails. + """ + # Example: "anxiety: 1.4" + try: + val_str = value.split(':', 1)[1].strip() + if val_str.lower() == "missing": + return None + return float(val_str) + except: + return None + +def convert_age(value: str): + """ + Convert the age string value after colon to a float (continuous measure). + Returns None if conversion fails. + """ + # Example: "age (yrs): 76" + try: + val_str = value.split(':', 1)[1].strip() + return float(val_str) + except: + return None + +def convert_gender(value: str): + """ + Convert the gender string value after colon to binary (female=0, male=1). + The data is stored as 'female: 0' or 'female: 1'. + 'female: 1' means the subject is female -> 0 + 'female: 0' means the subject is male -> 1 + Returns None if conversion fails. + """ + try: + val_str = value.split(':', 1)[1].strip() + if val_str == "1": + return 0 # female + elif val_str == "0": + return 1 # male + return None + except: + return None + +# 3. Save metadata with initial filtering +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical feature extraction if trait_row is not None +if trait_row is not None: + # Assume "clinical_data" is the DataFrame containing sample characteristics + # from a previous step in the pipeline + selected_clinical = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + preview = preview_df(selected_clinical, n=5, max_items=200) + # Optionally observe the preview (not printing to avoid extra text, but you could if needed) + selected_clinical.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the observed identifiers, some (like "A2BP1", "7A5") appear to be old or non-standard. +# Hence, they likely need to be mapped to official gene symbols. + +requires_gene_mapping = True +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1) Identify columns in `gene_annotation` corresponding to probe IDs and gene symbols. +# From the previous preview, "ID" in the gene annotation matches the expression data's IDs, +# and "ORF" appears to hold the same text which we'll treat as the gene symbol column. + +# 2) Get the gene mapping dataframe. +mapping_df = get_gene_mapping(annotation=gene_annotation, prob_col='ID', gene_col='ORF') + +# 3) Apply mapping to convert probe-level measurements to gene-level expression. +gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df) + +# (Optional) Print basic info to confirm successful mapping. +print("Mapped gene data shape:", gene_data.shape) +print("First 20 mapped gene symbols:", list(gene_data.index[:20])) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Ensure "selected_clinical" is defined by reading from our previously saved CSV. +temp_df = pd.read_csv(out_clinical_data_file) +# Step 2 extracts trait, age, gender => we expect exactly 3 rows +if temp_df.shape[0] == 3: + temp_df.index = [trait, "Age", "Gender"] +selected_clinical = temp_df + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 3. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 4. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 6. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE78104.py b/p1/preprocess/Anxiety_disorder/code/GSE78104.py new file mode 100644 index 0000000000000000000000000000000000000000..fd7f95d6d96564bf70b8dc09c80bdc12f9771292 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE78104.py @@ -0,0 +1,188 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE78104" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE78104" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE78104.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE78104.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE78104.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # From the background info (lncRNA + mRNA microarray), it's likely gene expression data is available. + +# 2. Variable Availability and Data Type Conversion +# Based on the sample characteristics dictionary: +# Row 1 => "disease state: Obsessive-Compulsive Disorder" or "normal control" +# We interpret OCD as part of "Anxiety_disorder" (1) vs normal (0). +trait_row = 1 +# Row 2 => "gender: male" or "gender: female" +gender_row = 2 +# Row 3 => "age: 25y", "23y", "18y", etc. +age_row = 3 + +# Define conversion functions +def convert_trait(value: str): + """Convert a disease state value into binary, mapping OCD to 1 and normal control to 0.""" + if ":" in value: + value = value.split(":", 1)[1].strip().lower() + if "compulsive" in value: + return 1 + elif "normal" in value: + return 0 + return None + +def convert_age(value: str): + """Convert age string like 'age: 25y' into an integer.""" + if ":" in value: + value = value.split(":", 1)[1].strip().lower() + value = value.replace("y", "") # remove trailing 'y' + try: + return float(value) + except ValueError: + return None + +def convert_gender(value: str): + """Convert gender string like 'gender: male'/'gender: female' into binary, female->0, male->1.""" + if ":" in value: + value = value.split(":", 1)[1].strip().lower() + if value == "male": + return 1 + elif value == "female": + return 0 + return None + +# 3. Save Metadata (Initial filtering) +is_trait_available = trait_row is not None +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction (only if trait data is available) +if trait_row is not None: + clinical_selected = geo_select_clinical_features( + clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + preview = preview_df(clinical_selected) + print("Preview of selected clinical features:") + print(preview) + clinical_selected.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the identifiers, they do not appear to be standard human gene symbols. +# Therefore, they likely need to be mapped. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify which annotation columns match the gene expression data's "ID" and which contain the gene symbol. +# From our observation, the annotation column "ID" matches the gene expression data "ID", +# and "GeneSymbol" contains the gene symbol information. + +# 2. Get a mapping dataframe with those columns. +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='GeneSymbol') + +# 3. Convert probe-level measurements to gene-level measurements. +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Ensure sample IDs in clinical and gene data match +def unify_sample_ids(df): + df.columns = df.columns.astype(str).str.strip().str.strip('"') + df.columns = df.columns.str.replace(r'\.CEL.*$', '', regex=True) + return df + +selected_clinical = unify_sample_ids(clinical_selected) +normalized_gene_data = unify_sample_ids(normalized_gene_data) + +common_samples = set(selected_clinical.columns).intersection(normalized_gene_data.columns) +if len(common_samples) == 0: + print("Warning: No matching sample IDs were found. The dataset may be misaligned.") +selected_clinical = selected_clinical.loc[:, list(common_samples)] +normalized_gene_data = normalized_gene_data.loc[:, list(common_samples)] + +# 3. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 4. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 5. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 6. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Cohort data processed with ID alignment fix." +) + +# 7. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/GSE94119.py b/p1/preprocess/Anxiety_disorder/code/GSE94119.py new file mode 100644 index 0000000000000000000000000000000000000000..fd4400725fec77b5f9a580f1205ef303b8d30396 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/GSE94119.py @@ -0,0 +1,153 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" +cohort = "GSE94119" + +# Input paths +in_trait_dir = "../DATA/GEO/Anxiety_disorder" +in_cohort_dir = "../DATA/GEO/Anxiety_disorder/GSE94119" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/GSE94119.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/GSE94119.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/GSE94119.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # Based on the background info (Illumina HT-12v4 BeadChip microarray) + +# 2. Variable Availability and Data Type Conversion +# From the sample characteristics, we see: +# - trait (Anxiety_disorder): Not explicitly in the dictionary, and all are anxiety patients => no variation +# - age: Not found in the dictionary +# - gender: Key 0 with 'FEMALE' and 'MALE' + +trait_row = None # No variation or row for Anxiety_disorder +age_row = None # No row for age +gender_row = 0 # gender is stored in key 0 + +# Define converter functions +def convert_trait(value: str): + # Not used here because trait is not available; return None + return None + +def convert_age(value: str): + # Not used here because age_row is None; return None + return None + +def convert_gender(value: str): + # Example values like "gender: FEMALE" or "gender: MALE" + parts = value.split(":") + if len(parts) < 2: + return None + gender_str = parts[1].strip().upper() + if gender_str == "FEMALE": + return 0 + elif gender_str == "MALE": + return 1 + else: + return None + +# 3. Save Metadata (initial filtering) +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Only if trait_row is not None (which it isn't). So skip. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the listed Illumina probe IDs (e.g., ILMN_1651228), these are not human gene symbols. +# They will require mapping to get the official gene symbols. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify the relevant columns in the gene annotation dataframe. +# From the preview, we see "ID" holds the Illumina identifiers (matching the expression data index), +# and "Symbol" holds the gene symbols. + +# 2. Extract the mapping between probe IDs and gene symbols. +mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Symbol") + +# 3. Convert probe-level measurements to gene-level expression using apply_gene_mapping. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# (Optionally, you might preview or inspect the resulting gene_data here if needed) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Since we do not have a trait_row (it was None), there's no separate "selected_clinical". +# We'll just reuse the clinical_data from previous steps. +selected_clinical = clinical_data + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 3 & 4. We skip trait-based missing-value handling and bias checks since there's no trait. + +# 5. Conduct final quality validation and save metadata +# Since the trait is not available, set is_trait_available=False. +# We must also provide is_biased=False to comply with validate_and_save_cohort_info's requirement when is_final=True. +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, + is_biased=False, # No trait to judge bias. + df=linked_data, + note="No trait data available in this cohort." +) + +# 6. If the dataset is deemed usable (unlikely here without trait), save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/code/TCGA.py b/p1/preprocess/Anxiety_disorder/code/TCGA.py new file mode 100644 index 0000000000000000000000000000000000000000..a71d07a94291832c7d878f3b8ce6bc3bea7793c0 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/code/TCGA.py @@ -0,0 +1,57 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Anxiety_disorder" + +# Input paths +tcga_root_dir = "../DATA/TCGA" + +# Output paths +out_data_file = "./output/preprocess/1/Anxiety_disorder/TCGA.csv" +out_gene_data_file = "./output/preprocess/1/Anxiety_disorder/gene_data/TCGA.csv" +out_clinical_data_file = "./output/preprocess/1/Anxiety_disorder/clinical_data/TCGA.csv" +json_path = "./output/preprocess/1/Anxiety_disorder/cohort_info.json" + +import os +import pandas as pd + +# 1. Identify the relevant subdirectory for the trait "Obesity" +subdirectories = [ + 'CrawlData.ipynb', '.DS_Store', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', + 'TCGA_Uterine_Carcinosarcoma_(UCS)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Thymoma_(THYM)', + 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Sarcoma_(SARC)', + 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', + 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Ocular_melanomas_(UVM)', + 'TCGA_Mesothelioma_(MESO)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', + 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lower_Grade_Glioma_(LGG)', + 'TCGA_Liver_Cancer_(LIHC)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', + 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', + 'TCGA_Glioblastoma_(GBM)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Endometrioid_Cancer_(UCEC)', + 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Cervical_Cancer_(CESC)', + 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Bile_Duct_Cancer_(CHOL)', + 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Acute_Myeloid_Leukemia_(LAML)' +] + +trait_keyword = trait +target_subdir = None + +for sd in subdirectories: + if trait_keyword.lower() in sd.lower(): + target_subdir = sd + break + +if target_subdir is None: + # No suitable data found for this trait; mark as completed + print("No TCGA subdirectory found for the trait. Skipping.") +else: + # 2. Locate clinical and genetic data files + cohort_dir = os.path.join(tcga_root_dir, target_subdir) + clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) + + # 3. Load the data + clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t') + genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t') + + # 4. Print column names of clinical data + print(clinical_df.columns) \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/cohort_info.json b/p1/preprocess/Anxiety_disorder/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..86037afeb9f8247ed452093941006a0c938cb5c8 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/cohort_info.json @@ -0,0 +1 @@ +{"GSE94119": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "No trait data available in this cohort."}, "GSE78104": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data processed with ID alignment fix."}, "GSE68526": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}, "GSE61672": {"is_usable": false, "is_gene_available": true, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}, "GSE60491": {"is_usable": false, "is_gene_available": true, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}, "GSE60190": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data is unavailable for this cohort."}, "GSE119995": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data not available; skipping linking and final dataset output."}} \ No newline at end of file diff --git a/p1/preprocess/Anxiety_disorder/gene_data/GSE119995.csv b/p1/preprocess/Anxiety_disorder/gene_data/GSE119995.csv new file mode 100644 index 0000000000000000000000000000000000000000..019bcdb661e55d2cefa905d2970f720730409000 --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/gene_data/GSE119995.csv @@ -0,0 +1 @@ +Gene,GSM3391438,GSM3391439,GSM3391440,GSM3391441,GSM3391442,GSM3391443,GSM3391444,GSM3391445,GSM3391446,GSM3391447,GSM3391448,GSM3391449,GSM3391450,GSM3391451,GSM3391452,GSM3391453,GSM3391454,GSM3391455,GSM3391456,GSM3391457,GSM3391458,GSM3391459,GSM3391460,GSM3391461,GSM3391462,GSM3391463,GSM3391464,GSM3391465,GSM3391466,GSM3391467,GSM3391468,GSM3391469,GSM3391470,GSM3391471,GSM3391472,GSM3391473,GSM3391474,GSM3391475,GSM3391476,GSM3391477,GSM3391478,GSM3391479,GSM3391480,GSM3391481,GSM3391482,GSM3391483,GSM3391484,GSM3391485,GSM3391486,GSM3391487,GSM3391488,GSM3391489,GSM3391490,GSM3391491,GSM3391492,GSM3391493,GSM3391494,GSM3391495,GSM3391496,GSM3391497,GSM3391498,GSM3391499,GSM3391500,GSM3391501,GSM3391502,GSM3391503,GSM3391504,GSM3391505,GSM3391506,GSM3391507,GSM3391508,GSM3391509 diff --git a/p1/preprocess/Anxiety_disorder/gene_data/GSE60190.csv b/p1/preprocess/Anxiety_disorder/gene_data/GSE60190.csv new file mode 100644 index 0000000000000000000000000000000000000000..0ad04b0f87a53bc4ecf7fa48871fccbb8837b3ec --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/gene_data/GSE60190.csv @@ -0,0 +1 @@ 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a/p1/preprocess/Anxiety_disorder/gene_data/GSE94119.csv b/p1/preprocess/Anxiety_disorder/gene_data/GSE94119.csv new file mode 100644 index 0000000000000000000000000000000000000000..44f443cdd0d0442331dbbfabf93ecc2097e9614c --- /dev/null +++ b/p1/preprocess/Anxiety_disorder/gene_data/GSE94119.csv @@ -0,0 +1 @@ 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+ +# Output paths +out_data_file = "./output/preprocess/1/Arrhythmia/GSE115574.csv" +out_gene_data_file = "./output/preprocess/1/Arrhythmia/gene_data/GSE115574.csv" +out_clinical_data_file = "./output/preprocess/1/Arrhythmia/clinical_data/GSE115574.csv" +json_path = "./output/preprocess/1/Arrhythmia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# Step 1: Determine if gene expression data is available +is_gene_available = True # Based on the background info (Affymetrix human gene expression microarrays) + +# Step 2: Identify data availability and define conversion functions + +# After reviewing the sample characteristics dictionary: +# {0: ['disease state: atrial fibrillation patient with severe mitral regurgitation', +# 'disease state: sinus rhythm patient with severe mitral regurgitation'], +# 1: ['tissue: left atrium - heart', +# 'tissue: right atrium - heart']} + +# The "trait" 'Arrhythmia' can be inferred from row 0, which distinguishes AFib vs. sinus rhythm. +trait_row = 0 + +# Age and gender data are not apparent in the dictionary, so set them to None. +age_row = None +gender_row = None + +def convert_trait(value): + """ + Convert the disease state string to a binary indicator for arrhythmia (AFib). + Return 1 if the string indicates atrial fibrillation, 0 if sinus rhythm, else None. + """ + try: + after_colon = value.split(':', 1)[1].strip().lower() + except IndexError: + return None + + if 'atrial fibrillation' in after_colon: + return 1 + elif 'sinus rhythm' in after_colon: + return 0 + return None + +def convert_age(value): + """ + Age data is not available in this dataset. Return None. + """ + return None + +def convert_gender(value): + """ + Gender data is not available in this dataset. Return None. + """ + return None + +# Step 3: Conduct initial filtering and save metadata +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# Step 4: If trait data is available, extract clinical features and save +if trait_row is not None: + selected_clinical_df = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + preview_result = preview_df(selected_clinical_df, n=5) + selected_clinical_df.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# These identifiers (e.g., '1007_s_at', '1053_at') are Affymetrix probe IDs, not standard gene symbols. +# Therefore, mapping to gene symbols is required. + +requires_gene_mapping = True +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# Gene Identifier Mapping + +# 1. Identify the columns in 'gene_annotation' that match the probe IDs in 'gene_data' and the gene symbols. +# From the preview, the probe ID is stored in column "ID", and gene symbols are stored in "Gene Symbol". + +# 2. Extract the gene mapping dataframe. +mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Gene Symbol") + +# 3. Convert probe-level measurements to gene expression data. +gene_data = apply_gene_mapping(gene_data, mapping_df) + +# For verification, let's print the new gene_data shape and a sample of its row indices. +print("Mapped gene_data shape:", gene_data.shape) +print("Sample gene symbols:", list(gene_data.index[:10])) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) + +# 3. Handle missing values in the linked data +linked_data = handle_missing_values(linked_data, trait_col=trait) + +# 4. Determine whether the trait/demographic features are severely biased +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait=trait) + +# 5. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Trait data and gene data successfully linked." +) + +# 6. If the dataset is deemed usable, save the final linked data as a CSV file +if is_usable: + linked_data.to_csv(out_data_file) + print(f"Saved final linked data to {out_data_file}") +else: + print("Dataset was not deemed usable; final linked data not saved.") \ No newline at end of file diff --git a/p1/preprocess/Arrhythmia/code/GSE41177.py b/p1/preprocess/Arrhythmia/code/GSE41177.py new file mode 100644 index 0000000000000000000000000000000000000000..a012a8403f7abb63e4964171b57f49009ba87593 --- /dev/null +++ b/p1/preprocess/Arrhythmia/code/GSE41177.py @@ -0,0 +1,158 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Arrhythmia" +cohort = "GSE41177" + +# Input paths +in_trait_dir = "../DATA/GEO/Arrhythmia" +in_cohort_dir = "../DATA/GEO/Arrhythmia/GSE41177" + +# Output paths +out_data_file = "./output/preprocess/1/Arrhythmia/GSE41177.csv" +out_gene_data_file = "./output/preprocess/1/Arrhythmia/gene_data/GSE41177.csv" +out_clinical_data_file = "./output/preprocess/1/Arrhythmia/clinical_data/GSE41177.csv" +json_path = "./output/preprocess/1/Arrhythmia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +# Based on the background info ("microarray analysis..."), we consider that +# this dataset likely contains gene expression data. +is_gene_available = True + +# 2.1 Data Availability +# The trait (arrhythmia) appears to be constant in all samples (all have AF), +# hence it's not useful for association studies. +trait_row = None +# The 'age' variable is found at key=2 with multiple distinct values. +age_row = 2 +# The 'gender' variable is found at key=1 with multiple distinct values. +gender_row = 1 + +# 2.2 Data Type Conversion +def convert_trait(value: str): + # The trait is not actually available (constant across all samples), + # so we return None here. + return None + +def convert_age(value: str): + # Example entry: "age: 62Y" + # We parse the substring after ':' then remove 'Y' and convert to float. + try: + parts = value.split(':', 1) + age_str = parts[1].replace('Y', '').strip() if len(parts) > 1 else '' + return float(age_str) + except: + return None + +def convert_gender(value: str): + # Example entry: "gender: male" + # Convert female -> 0, male -> 1 + parts = value.split(':', 1) + g_str = parts[1].strip().lower() if len(parts) > 1 else '' + if g_str == 'male': + return 1 + elif g_str == 'female': + return 0 + return None + +# 3. Save Metadata (Initial Filtering) +# trait_row is None => trait data is not available +is_trait_available = (trait_row is not None) +is_usable = validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, we skip the clinical feature extraction step. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the given probe IDs (e.g., "1007_s_at", "1053_at"), they are Affymetrix probe set IDs and not human gene symbols. +# Therefore, gene mapping to human gene symbols is required. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. Identify the columns corresponding to the probe identifiers and the gene symbols +# From the annotation preview, the 'ID' column matches the probe identifiers in our gene_data, +# and the 'Gene Symbol' column stores the gene symbols. + +probe_col = "ID" +symbol_col = "Gene Symbol" + +# 2. Extract the gene mapping DataFrame using the library function +gene_mapping_df = get_gene_mapping(gene_annotation, probe_col, symbol_col) + +# 3. Convert probe-level measurements to gene-level expression data +gene_data = apply_gene_mapping(gene_data, gene_mapping_df) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Since trait_row is None (trait is not available), we cannot link clinical data or perform trait-based analysis. +# We'll skip linking and bias evaluation of the trait. + +# We'll still perform the final validation to record that this cohort lacks trait data. +placeholder_df = pd.DataFrame() # Empty placeholder +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, # trait not available + is_biased=False, # No trait → can't evaluate trait bias, set to False to proceed + df=placeholder_df, # Required argument, though empty + note="No trait data available in the cohort." +) + +# If the dataset is usable (unlikely since trait is missing), we would save final linked data. +if is_usable: + # Normally we would have a "linked_data" DataFrame to save; + # however, there's no trait, so no final data is produced. + pass +else: + print("Trait not available; skipping final data linkage and output.") \ No newline at end of file diff --git a/p1/preprocess/Arrhythmia/code/GSE47727.py b/p1/preprocess/Arrhythmia/code/GSE47727.py new file mode 100644 index 0000000000000000000000000000000000000000..fb028d4baf07ea00eeacdbbdcf7c3daafedab2f9 --- /dev/null +++ b/p1/preprocess/Arrhythmia/code/GSE47727.py @@ -0,0 +1,170 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Arrhythmia" +cohort = "GSE47727" + +# Input paths +in_trait_dir = "../DATA/GEO/Arrhythmia" +in_cohort_dir = "../DATA/GEO/Arrhythmia/GSE47727" + +# Output paths +out_data_file = "./output/preprocess/1/Arrhythmia/GSE47727.csv" +out_gene_data_file = "./output/preprocess/1/Arrhythmia/gene_data/GSE47727.csv" +out_clinical_data_file = "./output/preprocess/1/Arrhythmia/clinical_data/GSE47727.csv" +json_path = "./output/preprocess/1/Arrhythmia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1. Gene Expression Data Availability +is_gene_available = True # The platform is Illumina HumanHT-12, indicating gene expression data. + +# 2. Variable Availability and Data Type Conversion + +# Based on the sample characteristics: +# 0 -> "age (yrs): X" +# 1 -> "gender: male"/"gender: female" +# 2 -> "tissue: blood" +# +# There's no indication (key) that provides Arrhythmia status; all subjects are "control participants." +# Thus, the trait is NOT available in this dataset. +trait_row = None +age_row = 0 +gender_row = 1 + +# Data type conversion functions +def convert_trait(x: str): + """ + For demonstration, we define the conversion but this dataset + has no trait data. We return None to indicate unavailability. + """ + return None + +def convert_age(x: str): + """ + Extract the numeric age after 'age (yrs):' and convert to float. + If there is any parsing error, return None. + """ + # Typically, these entries look like "age (yrs): 67" + # We split by ':' and strip. + try: + val = x.split(':')[-1].strip() + return float(val) + except: + return None + +def convert_gender(x: str): + """ + Convert 'gender: female' -> 0 and 'gender: male' -> 1. + If other strings appear, return None. + """ + try: + val = x.split(':')[-1].strip().lower() + if val == 'male': + return 1 + elif val == 'female': + return 0 + except: + pass + return None + +# 3. Save Metadata +# Perform initial filtering (is_final=False). Since trait_row is None, +# trait data is NOT available. +is_trait_available = False + +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4. Clinical Feature Extraction +# Since trait_row is None, we skip extracting clinical features. +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# The gene identifiers (e.g., "ILMN_1343291") are Illumina probe IDs, not standard human gene symbols. +# Thus, they require mapping to gene symbols. + +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP: Gene Identifier Mapping + +# 1. We identify that in the gene_annotation DataFrame: +# - The "ID" column matches the Illumina probe IDs (e.g., "ILMN_1343291") found in gene_data.index. +# - The "Symbol" column holds gene symbol information for mapping. + +# 2. Get a gene mapping DataFrame from gene_annotation by selecting the 'ID' column as the probe identifier +# and the 'Symbol' column as the gene symbol. +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Symbol') + +# 3. Convert probe-level measurements in gene_data to gene-level measurements +# by applying the gene mapping, handling probes with multiple gene mappings. +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +import pandas as pd + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# Since trait_row is None (trait is not available), we cannot link clinical data or perform trait-based analysis. +# We'll skip linking and bias evaluation of the trait. + +# We'll still perform the final validation to record that this cohort lacks trait data. +placeholder_df = pd.DataFrame() # Empty placeholder +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=False, # trait not available + is_biased=False, # No trait → can't evaluate trait bias, set to False to proceed + df=placeholder_df, # Required argument, though empty + note="No trait data available in the cohort." +) + +# If the dataset is usable (unlikely since trait is missing), we would save final linked data. +if is_usable: + # Normally we would have a "linked_data" DataFrame to save; + # however, there's no trait, so no final data is produced. + pass +else: + print("Trait not available; skipping final data linkage and output.") \ No newline at end of file diff --git a/p1/preprocess/Arrhythmia/code/GSE53622.py b/p1/preprocess/Arrhythmia/code/GSE53622.py new file mode 100644 index 0000000000000000000000000000000000000000..8bb93aed51776dff05d79cc703d8391f425a23a4 --- /dev/null +++ b/p1/preprocess/Arrhythmia/code/GSE53622.py @@ -0,0 +1,176 @@ +# Path Configuration +from tools.preprocess import * + +# Processing context +trait = "Arrhythmia" +cohort = "GSE53622" + +# Input paths +in_trait_dir = "../DATA/GEO/Arrhythmia" +in_cohort_dir = "../DATA/GEO/Arrhythmia/GSE53622" + +# Output paths +out_data_file = "./output/preprocess/1/Arrhythmia/GSE53622.csv" +out_gene_data_file = "./output/preprocess/1/Arrhythmia/gene_data/GSE53622.csv" +out_clinical_data_file = "./output/preprocess/1/Arrhythmia/clinical_data/GSE53622.csv" +json_path = "./output/preprocess/1/Arrhythmia/cohort_info.json" + +# STEP 1 + +from tools.preprocess import * + +# 1. Identify the paths to the SOFT file and the matrix file +soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) + +# 2. Read the matrix file to obtain background information and sample characteristics data +background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] +clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] +background_info, clinical_data = get_background_and_clinical_data( + matrix_file, + background_prefixes, + clinical_prefixes +) + +# 3. Obtain the sample characteristics dictionary from the clinical dataframe +sample_characteristics_dict = get_unique_values_by_row(clinical_data) + +# 4. Explicitly print out all the background information and the sample characteristics dictionary +print("Background Information:") +print(background_info) +print("\nSample Characteristics Dictionary:") +print(sample_characteristics_dict) +# 1) Determine if gene expression data is available +is_gene_available = True # This is an lncRNA microarray study, so we consider it to have gene expression + +# 2) Identify data availability and create conversion functions + +# The sample characteristics dictionary shows: +# trait appears in row 10 with values "arrhythmia: no" or "arrhythmia: yes" +trait_row = 10 + +# age appears in row 1 with multiple numeric values +age_row = 1 + +# gender appears in row 2 with values "Sex: female" or "Sex: male" +gender_row = 2 + +def convert_trait(raw_value: str): + """ + Convert arrhythmia values ('yes'/'no') to binary (1/0). + """ + value = raw_value.split(':')[-1].strip().lower() + if value == 'yes': + return 1 + elif value == 'no': + return 0 + return None + +def convert_age(raw_value: str): + """ + Convert age values to float. If conversion fails, returns None. + """ + value = raw_value.split(':')[-1].strip() + try: + return float(value) + except: + return None + +def convert_gender(raw_value: str): + """ + Convert gender values ('male'/'female') to binary (1/0). + """ + value = raw_value.split(':')[-1].strip().lower() + if value == 'male': + return 1 + elif value == 'female': + return 0 + return None + +# 3) Save metadata using initial filtering +is_trait_available = (trait_row is not None) +validate_and_save_cohort_info( + is_final=False, + cohort=cohort, + info_path=json_path, + is_gene_available=is_gene_available, + is_trait_available=is_trait_available +) + +# 4) Extract clinical features if trait data is available +if trait_row is not None: + selected_clinical_features = geo_select_clinical_features( + clinical_df=clinical_data, + trait=trait, + trait_row=trait_row, + convert_trait=convert_trait, + age_row=age_row, + convert_age=convert_age, + gender_row=gender_row, + convert_gender=convert_gender + ) + + # Preview and save extracted clinical data + preview_result = preview_df(selected_clinical_features, n=5) + print("Preview of Selected Clinical Data:", preview_result) + selected_clinical_features.to_csv(out_clinical_data_file, index=False) +# STEP3 +# 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. +gene_data = get_genetic_data(matrix_file) + +# 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. +print(gene_data.index[:20]) +# Based on the numeric format of the identifiers, they do not appear to match standard human gene symbols. +# Therefore, gene mapping is needed. +print("requires_gene_mapping = True") +# STEP5 +# 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. +gene_annotation = get_gene_annotation(soft_file) + +# 2. Use the 'preview_df' function from the library to preview the data and print out the results. +print("Gene annotation preview:") +print(preview_df(gene_annotation)) +# STEP 6: Gene Identifier Mapping + +# 1. From observation, the 'ID' column in 'gene_annotation' matches the gene expression data 'ID'. +# The 'SPOT_ID' column holds the gene symbols (though they look unusual, we assume they contain relevant symbol info). +mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='SPOT_ID') + +# 2. Convert probe-level measurements to gene-level expression data using the mapping. +gene_data = apply_gene_mapping(gene_data, mapping_df) +# STEP 7: Data Normalization and Linking + +# 1. Normalize gene symbols in the obtained gene expression data +normalized_gene_data = normalize_gene_symbols_in_index(gene_data) +normalized_gene_data.to_csv(out_gene_data_file) +print(f"Saved normalized gene data to {out_gene_data_file}") + +# 2. We refer to the clinical data variable from step 2 as 'selected_clinical_features' +selected_clinical = selected_clinical_features + +# 3. Link the clinical and genetic data on sample IDs +linked_data = geo_link_clinical_genetic_data(selected_clinical, normalized_gene_data) + +# 4. Handle missing values, removing or imputing as instructed +linked_data = handle_missing_values(linked_data, trait) + +# 5. Determine whether the trait (and potentially other features) is severely biased. +trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) + +# 6. Conduct final quality validation and save metadata +is_usable = validate_and_save_cohort_info( + is_final=True, + cohort=cohort, + info_path=json_path, + is_gene_available=True, + is_trait_available=True, + is_biased=trait_biased, + df=linked_data, + note="Cohort data successfully processed with trait-based analysis." +) + +# 7. If the dataset is usable, save the final linked data +if is_usable: + linked_data.to_csv(out_data_file, index=True) + print(f"Saved final linked data to {out_data_file}") +else: + print("The dataset is not usable for trait-based association. Skipping final output.") \ No newline at end of file diff --git a/p1/preprocess/Arrhythmia/cohort_info.json b/p1/preprocess/Arrhythmia/cohort_info.json new file mode 100644 index 0000000000000000000000000000000000000000..3fc820650163a82215677f22f69d521dee122b47 --- /dev/null +++ b/p1/preprocess/Arrhythmia/cohort_info.json @@ -0,0 +1 @@ +{"GSE93101": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}, "GSE55231": {"is_usable": false, "is_gene_available": true, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}, "GSE53622": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Cohort data successfully processed with trait-based analysis."}, "GSE47727": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "No trait data available in the cohort."}, "GSE41177": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "No trait data available in the cohort."}, "GSE235307": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data is available; completed linking and preprocessing."}, "GSE182600": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data and gene data successfully linked."}, "GSE143924": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data and gene data successfully linked."}, "GSE136992": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data not found; dataset is not usable."}, "GSE115574": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "Trait data and gene data successfully linked."}} \ No newline at end of file diff --git a/p1/preprocess/Arrhythmia/gene_data/GSE182600.csv b/p1/preprocess/Arrhythmia/gene_data/GSE182600.csv new file mode 100644 index 0000000000000000000000000000000000000000..29a9f84dd504935c86c6c0262a285a5ddf15cbf8 --- /dev/null +++ b/p1/preprocess/Arrhythmia/gene_data/GSE182600.csv @@ -0,0 +1 @@ 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