# Path Configuration
from tools.preprocess import *

# Processing context
trait = "Bipolar_disorder"

# Input paths
tcga_root_dir = "../DATA/TCGA"

# Output paths
out_data_file = "./output/preprocess/1/Bipolar_disorder/TCGA.csv"
out_gene_data_file = "./output/preprocess/1/Bipolar_disorder/gene_data/TCGA.csv"
out_clinical_data_file = "./output/preprocess/1/Bipolar_disorder/clinical_data/TCGA.csv"
json_path = "./output/preprocess/1/Bipolar_disorder/cohort_info.json"

import os
import pandas as pd

# Step 1: Check directories in tcga_root_dir for anything relevant to "Bipolar_disorder"
search_terms = ["bipolar", "bipolar_disorder", "mania"]
dir_list = os.listdir(tcga_root_dir)
matching_dir = None

for d in dir_list:
    d_lower = d.lower()
    if any(term in d_lower for term in search_terms):
        # Found a match, select this directory
        matching_dir = d
        break

if matching_dir is None:
    # No matching directory found. Mark the dataset as skipped.
    validate_and_save_cohort_info(
        is_final=False,
        cohort="TCGA",
        info_path=json_path,
        is_gene_available=False,
        is_trait_available=False
    )
else:
    # 2. Identify the clinicalMatrix and PANCAN files
    cohort_dir = os.path.join(tcga_root_dir, matching_dir)
    clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir)

    # 3. Load both data files
    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 the column names of the clinical data
    print("Clinical Data Columns:")
    print(clinical_df.columns.tolist())