Download output/preprocess/Depression/code/TCGA.py from Liu-Hy/GenoTEX: direct link, hf CLI and curl.
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| # Path Configuration | |
| from tools.preprocess import * | |
| # Processing context | |
| trait = "Depression" | |
| # Input paths | |
| tcga_root_dir = "../DATA/TCGA" | |
| # Output paths | |
| out_data_file = "./output/z2/preprocess/Depression/TCGA.csv" | |
| out_gene_data_file = "./output/z2/preprocess/Depression/gene_data/TCGA.csv" | |
| out_clinical_data_file = "./output/z2/preprocess/Depression/clinical_data/TCGA.csv" | |
| json_path = "./output/z2/preprocess/Depression/cohort_info.json" | |
| # Step 1: Initial Data Loading | |
| import os | |
| import pandas as pd | |
| # Step 1: Select TCGA subdirectory relevant to the trait "Depression" | |
| keywords = [ | |
| 'depress', 'mdd', 'major_depress', 'depressive', 'mood', | |
| 'psychi', 'mental', 'affective', 'sadness' | |
| ] | |
| subdirs = [d for d in os.listdir(tcga_root_dir) if os.path.isdir(os.path.join(tcga_root_dir, d))] | |
| matches = [] | |
| for d in subdirs: | |
| name_l = d.lower() | |
| if any(k in name_l for k in keywords): | |
| matches.append(d) | |
| selected_tcga_dir = None | |
| if len(matches) > 0: | |
| # Choose the most specific match by the longest directory name (heuristic for specificity) | |
| selected_tcga_dir = max(matches, key=len) | |
| else: | |
| # No suitable cohort for depression in TCGA cancer cohorts; record and skip this trait | |
| print("No suitable TCGA cohort found for trait 'Depression'. Skipping preprocessing for this trait.") | |
| _ = validate_and_save_cohort_info( | |
| is_final=False, | |
| cohort="TCGA", | |
| info_path=json_path, | |
| is_gene_available=False, | |
| is_trait_available=False | |
| ) | |
| # Step 2-4: If a directory was selected, identify files, load data, and print clinical column names | |
| clinical_df, genetic_df = None, None | |
| if selected_tcga_dir is not None: | |
| cohort_dir = os.path.join(tcga_root_dir, selected_tcga_dir) | |
| clinical_path, genetic_path = tcga_get_relevant_filepaths(cohort_dir) | |
| clinical_df = pd.read_csv(clinical_path, sep="\t", index_col=0, low_memory=False) | |
| genetic_df = pd.read_csv(genetic_path, sep="\t", index_col=0, low_memory=False) | |
| print(list(clinical_df.columns)) |