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from tools.preprocess import * |
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trait = "Endometriosis" |
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cohort = "GSE138297" |
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in_trait_dir = "../DATA/GEO/Endometriosis" |
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in_cohort_dir = "../DATA/GEO/Endometriosis/GSE138297" |
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out_data_file = "./output/preprocess/3/Endometriosis/GSE138297.csv" |
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out_gene_data_file = "./output/preprocess/3/Endometriosis/gene_data/GSE138297.csv" |
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out_clinical_data_file = "./output/preprocess/3/Endometriosis/clinical_data/GSE138297.csv" |
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json_path = "./output/preprocess/3/Endometriosis/cohort_info.json" |
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soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) |
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background_info, clinical_data = get_background_and_clinical_data(matrix_file) |
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sample_characteristics = get_unique_values_by_row(clinical_data) |
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print("Dataset Background Information:") |
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print(f"{background_info}\n") |
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print("Sample Characteristics:") |
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for feature, values in sample_characteristics.items(): |
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print(f"Feature: {feature}") |
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print(f"Values: {values}\n") |
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is_gene_available = False |
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trait_row = None |
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age_row = 3 |
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gender_row = 1 |
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def convert_trait(value): |
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return None |
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def convert_age(value): |
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if value is None: |
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return None |
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try: |
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return float(value.split(': ')[-1].strip()) |
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except: |
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return None |
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def convert_gender(value): |
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if value is None: |
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return None |
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try: |
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return int(value.split(': ')[-1].strip()) |
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except: |
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return None |
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validate_and_save_cohort_info(is_final=False, |
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cohort=cohort, |
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info_path=json_path, |
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is_gene_available=is_gene_available, |
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is_trait_available=trait_row is not None) |
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soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) |
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gene_data = get_genetic_data(matrix_file) |
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print("Shape of gene expression data:", gene_data.shape) |
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print("\nFirst few rows of data:") |
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print(gene_data.head()) |
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print("\nFirst 20 gene/probe identifiers:") |
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print(gene_data.index[:20]) |
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import gzip |
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with gzip.open(matrix_file, 'rt', encoding='utf-8') as f: |
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lines = [] |
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for i, line in enumerate(f): |
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if "!series_matrix_table_begin" in line: |
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for _ in range(5): |
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lines.append(next(f).strip()) |
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break |
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print("\nFirst few lines after matrix marker in raw file:") |
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for line in lines: |
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print(line) |
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requires_gene_mapping = True |
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gene_metadata = get_gene_annotation(soft_file) |
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print("Column names:", gene_metadata.columns.tolist()) |
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print("\nFirst few rows preview:") |
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print(preview_df(gene_metadata)) |
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soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) |
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gene_data = get_genetic_data(matrix_file) |
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mapping_data = get_gene_mapping(gene_metadata, 'ID', 'gene_assignment') |
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gene_data = apply_gene_mapping(gene_data, mapping_data) |
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gene_data = normalize_gene_symbols_in_index(gene_data) |
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gene_data = normalize_gene_symbols_in_index(gene_data) |
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gene_data.to_csv(out_gene_data_file) |
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is_usable = validate_and_save_cohort_info( |
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is_final=True, |
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cohort=cohort, |
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info_path=json_path, |
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is_gene_available=True, |
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is_trait_available=False, |
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is_biased=None, |
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df=None, |
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note="Dataset contains gene expression data but lacks endometriosis trait information." |
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) |