| |
| from tools.preprocess import * |
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| |
| trait = "Epilepsy" |
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| |
| tcga_root_dir = "../DATA/TCGA" |
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| |
| out_data_file = "./output/z3/preprocess/Epilepsy/TCGA.csv" |
| out_gene_data_file = "./output/z3/preprocess/Epilepsy/gene_data/TCGA.csv" |
| out_clinical_data_file = "./output/z3/preprocess/Epilepsy/clinical_data/TCGA.csv" |
| json_path = "./output/z3/preprocess/Epilepsy/cohort_info.json" |
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| |
| import os |
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| |
| synonyms = ["epilepsy", "seizure", "seizures", "ictal", "epileptic"] |
| all_dirs = [d for d in os.listdir(tcga_root_dir) if os.path.isdir(os.path.join(tcga_root_dir, d))] |
| matched_dirs = [d for d in all_dirs if any(s in d.lower() for s in synonyms)] |
|
|
| selected_cohort_dirname = None |
| if matched_dirs: |
| |
| prioritized = sorted(matched_dirs, key=lambda d: (0 if "epilepsy" in d.lower() else 1, d.lower())) |
| selected_cohort_dirname = prioritized[0] |
|
|
| if selected_cohort_dirname is None: |
| print("No suitable TCGA cohort found for the trait 'Epilepsy'. Skipping this trait.") |
| |
| _ = validate_and_save_cohort_info( |
| is_final=False, |
| cohort="TCGA", |
| info_path=json_path, |
| is_gene_available=False, |
| is_trait_available=False |
| ) |
| clinical_df = None |
| gene_df = None |
| else: |
| |
| cohort_dir = os.path.join(tcga_root_dir, selected_cohort_dirname) |
| clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir) |
|
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| |
| clinical_df = pd.read_csv(clinical_file_path, sep='\t', index_col=0, low_memory=False, compression='infer') |
| gene_df = pd.read_csv(genetic_file_path, sep='\t', index_col=0, low_memory=False, compression='infer') |
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| |
| print(list(clinical_df.columns)) |