# Path Configuration from tools.preprocess import * # Processing context trait = "Bipolar_disorder" # Input paths tcga_root_dir = "../DATA/TCGA" # Output paths out_data_file = "./output/z1/preprocess/Bipolar_disorder/TCGA.csv" out_gene_data_file = "./output/z1/preprocess/Bipolar_disorder/gene_data/TCGA.csv" out_clinical_data_file = "./output/z1/preprocess/Bipolar_disorder/clinical_data/TCGA.csv" json_path = "./output/z1/preprocess/Bipolar_disorder/cohort_info.json" # Step 1: Initial Data Loading import os import pandas as pd # Initialize placeholders for downstream steps selected_subdir = None clinical_df = None genetic_df = None # Discover subdirectories try: subdirs = [d for d in os.listdir(tcga_root_dir) if os.path.isdir(os.path.join(tcga_root_dir, d))] except Exception as e: subdirs = [] print(f"ERROR: Unable to list TCGA root directory '{tcga_root_dir}': {e}") # Attempt to find a TCGA cohort relevant to Bipolar disorder (unlikely within TCGA cancer cohorts) trait_keywords = { "bipolar", "bipolar_disorder", "bipolar disorder", "mania", "manic" } candidates = [] for d in subdirs: name_l = d.lower() if any(k in name_l for k in trait_keywords): candidates.append(d) # Select the most specific match if any (longest name heuristic) if candidates: selected_subdir = sorted(candidates, key=len, reverse=True)[0] if selected_subdir is None: print(f"No suitable TCGA cohort found for trait '{trait}'. Skipping this trait.") # Record that this trait is not applicable for TCGA validate_and_save_cohort_info( is_final=False, cohort="TCGA", info_path=json_path, is_gene_available=False, is_trait_available=False ) else: cohort_dir = os.path.join(tcga_root_dir, selected_subdir) clinical_path, genetic_path = tcga_get_relevant_filepaths(cohort_dir) # Load dataframes 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 clinical column names for inspection print(list(clinical_df.columns))