{ "cells": [ { "cell_type": "code", "execution_count": 1, "id": "708581c4", "metadata": { "execution": { "iopub.execute_input": "2025-03-25T04:12:07.451679Z", "iopub.status.busy": "2025-03-25T04:12:07.451181Z", "iopub.status.idle": "2025-03-25T04:12:07.620868Z", "shell.execute_reply": "2025-03-25T04:12:07.620223Z" } }, "outputs": [], "source": [ "import sys\n", "import os\n", "sys.path.append(os.path.abspath(os.path.join(os.getcwd(), '../..')))\n", "\n", "# Path Configuration\n", "from tools.preprocess import *\n", "\n", "# Processing context\n", "trait = \"Thyroid_Cancer\"\n", "\n", "# Input paths\n", "tcga_root_dir = \"../../input/TCGA\"\n", "\n", "# Output paths\n", "out_data_file = \"../../output/preprocess/Thyroid_Cancer/TCGA.csv\"\n", "out_gene_data_file = \"../../output/preprocess/Thyroid_Cancer/gene_data/TCGA.csv\"\n", "out_clinical_data_file = \"../../output/preprocess/Thyroid_Cancer/clinical_data/TCGA.csv\"\n", "json_path = \"../../output/preprocess/Thyroid_Cancer/cohort_info.json\"\n" ] }, { "cell_type": "markdown", "id": "46ca9f29", "metadata": {}, "source": [ "### Step 1: Initial Data Loading" ] }, { "cell_type": "code", "execution_count": 2, "id": "06225c29", "metadata": { "execution": { "iopub.execute_input": "2025-03-25T04:12:07.622416Z", "iopub.status.busy": "2025-03-25T04:12:07.622269Z", "iopub.status.idle": "2025-03-25T04:12:09.061925Z", "shell.execute_reply": "2025-03-25T04:12:09.061464Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Looking for a relevant cohort directory for Thyroid_Cancer...\n", "Available cohorts: ['TCGA_Liver_Cancer_(LIHC)', 'TCGA_Lower_Grade_Glioma_(LGG)', 'TCGA_lower_grade_glioma_and_glioblastoma_(GBMLGG)', 'TCGA_Lung_Adenocarcinoma_(LUAD)', 'TCGA_Lung_Cancer_(LUNG)', 'TCGA_Lung_Squamous_Cell_Carcinoma_(LUSC)', 'TCGA_Melanoma_(SKCM)', 'TCGA_Mesothelioma_(MESO)', 'TCGA_Ocular_melanomas_(UVM)', 'TCGA_Ovarian_Cancer_(OV)', 'TCGA_Pancreatic_Cancer_(PAAD)', 'TCGA_Pheochromocytoma_Paraganglioma_(PCPG)', 'TCGA_Prostate_Cancer_(PRAD)', 'TCGA_Rectal_Cancer_(READ)', 'TCGA_Sarcoma_(SARC)', 'TCGA_Stomach_Cancer_(STAD)', 'TCGA_Testicular_Cancer_(TGCT)', 'TCGA_Thymoma_(THYM)', 'TCGA_Thyroid_Cancer_(THCA)', 'TCGA_Uterine_Carcinosarcoma_(UCS)', '.DS_Store', 'CrawlData.ipynb', 'TCGA_Acute_Myeloid_Leukemia_(LAML)', 'TCGA_Adrenocortical_Cancer_(ACC)', 'TCGA_Bile_Duct_Cancer_(CHOL)', 'TCGA_Bladder_Cancer_(BLCA)', 'TCGA_Breast_Cancer_(BRCA)', 'TCGA_Cervical_Cancer_(CESC)', 'TCGA_Colon_and_Rectal_Cancer_(COADREAD)', 'TCGA_Colon_Cancer_(COAD)', 'TCGA_Endometrioid_Cancer_(UCEC)', 'TCGA_Esophageal_Cancer_(ESCA)', 'TCGA_Glioblastoma_(GBM)', 'TCGA_Head_and_Neck_Cancer_(HNSC)', 'TCGA_Kidney_Chromophobe_(KICH)', 'TCGA_Kidney_Clear_Cell_Carcinoma_(KIRC)', 'TCGA_Kidney_Papillary_Cell_Carcinoma_(KIRP)', 'TCGA_Large_Bcell_Lymphoma_(DLBC)']\n", "Thyroid disease-related cohorts: ['TCGA_Thyroid_Cancer_(THCA)']\n", "Selected cohort: TCGA_Thyroid_Cancer_(THCA)\n", "Clinical data file: TCGA.THCA.sampleMap_THCA_clinicalMatrix\n", "Genetic data file: TCGA.THCA.sampleMap_HiSeqV2_PANCAN.gz\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "\n", "Clinical data columns:\n", "['_INTEGRATION', '_PATIENT', '_cohort', '_primary_disease', '_primary_site', 'additional_pharmaceutical_therapy', 'additional_radiation_therapy', 'additional_surgery_locoregional_procedure', 'age_at_initial_pathologic_diagnosis', 'bcr_followup_barcode', 'bcr_patient_barcode', 'bcr_sample_barcode', 'braf_gene_genotyping_outcome_lab_results_text', 'days_to_additional_surgery_metastatic_procedure', 'days_to_birth', 'days_to_collection', 'days_to_death', 'days_to_initial_pathologic_diagnosis', 'days_to_last_followup', 'days_to_new_tumor_event_additional_surgery_procedure', 'days_to_new_tumor_event_after_initial_treatment', 'extrathyroid_carcinoma_present_extension_status', 'first_degree_relative_history_thyrd_glnd_crcnm_dgnss_rltnshp_typ', 'followup_case_report_form_submission_reason', 'form_completion_date', 'gender', 'genotype_analysis_performed_indicator', 'genotyping_results_gene_mutation_not_reported_reason', 'histologic_disease_progression_present_indicator', 'histologic_disease_progression_present_type', 'histological_type', 'histological_type_other', 'history_of_neoadjuvant_treatment', 'i_131_first_administered_dose', 'i_131_subsequent_administered_dose', 'i_131_total_administered_dose', 'i_131_total_administered_preparation_technique', 'icd_10', 'icd_o_3_histology', 'icd_o_3_site', 'informed_consent_verified', 'initial_weight', 'is_ffpe', 'lost_follow_up', 'lymph_node_examined_count', 'lymph_node_preoperative_assessment_diagnostic_imaging_type', 'lymph_node_preoperative_scan_indicator', 'metastatic_neoplasm_confirmed_diagnosis_method_name', 'metastatic_neoplasm_confirmed_diagnosis_method_text', 'metastatic_site', 'neoplasm_depth', 'new_neoplasm_confirmed_diagnosis_method_name', 'new_neoplasm_event_occurrence_anatomic_site', 'new_neoplasm_event_type', 'new_neoplasm_occurrence_anatomic_site_text', 'new_tumor_event_additional_surgery_procedure', 'new_tumor_event_after_initial_treatment', 'number_of_lymphnodes_positive_by_he', 'oct_embedded', 'other_dx', 'other_genotyping_outcome_lab_results_text', 'other_metastatic_site', 'pathologic_M', 'pathologic_N', 'pathologic_T', 'pathologic_stage', 'pathology_report_file_name', 'patient_id', 'patient_personal_medical_history_thyroid_gland_disorder_name', 'patient_personal_medical_history_thyroid_other_specify_text', 'person_lifetime_risk_radiation_exposure_indicator', 'person_neoplasm_cancer_status', 'post_surgical_procedure_assessment_thyroid_gland_carcinoma_stats', 'postoperative_rx_tx', 'primary_lymph_node_presentation_assessment', 'primary_neoplasm_focus_type', 'primary_thyroid_gland_neoplasm_location_anatomic_site', 'radiation_therapy', 'radiation_therapy_administered_dose_text', 'radiation_therapy_administered_preparation_technique_text', 'radiosensitizing_agent_administered_indicator', 'ras_family_gene_genotyping_outcome_lab_results_text', 'residual_tumor', 'ret_ptc_rearrangement_genotyping_outcome_lab_results_text', 'sample_type', 'sample_type_id', 'system_version', 'targeted_molecular_therapy', 'therapeutic_procedure_new_neoplasm_required_additional_thrpy_typ', 'thyroid_gland_carcinoma_involvement_regional_lymph_node_type', 'tissue_prospective_collection_indicator', 'tissue_retrospective_collection_indicator', 'tissue_source_site', 'tumor_tissue_site', 'vial_number', 'vital_status', 'year_of_initial_pathologic_diagnosis', '_GENOMIC_ID_TCGA_THCA_exp_HiSeqV2_percentile', '_GENOMIC_ID_TCGA_THCA_hMethyl450', '_GENOMIC_ID_TCGA_THCA_mutation_bcm_gene', '_GENOMIC_ID_TCGA_THCA_RPPA', '_GENOMIC_ID_TCGA_THCA_exp_HiSeqV2', '_GENOMIC_ID_TCGA_THCA_gistic2', '_GENOMIC_ID_TCGA_THCA_PDMRNAseqCNV', '_GENOMIC_ID_TCGA_THCA_mutation_bcgsc_gene', '_GENOMIC_ID_TCGA_THCA_mutation', '_GENOMIC_ID_TCGA_THCA_PDMRNAseq', '_GENOMIC_ID_TCGA_THCA_mutation_broad_gene', '_GENOMIC_ID_TCGA_THCA_exp_HiSeqV2_exon', '_GENOMIC_ID_TCGA_THCA_miRNA_HiSeq', '_GENOMIC_ID_TCGA_THCA_exp_HiSeqV2_PANCAN', '_GENOMIC_ID_data/public/TCGA/THCA/miRNA_HiSeq_gene', '_GENOMIC_ID_TCGA_THCA_gistic2thd']\n", "\n", "Clinical data shape: (580, 113)\n", "Genetic data shape: (20530, 572)\n" ] } ], "source": [ "import os\n", "\n", "# Check if there's a suitable cohort directory for Thyroid_Cancer\n", "print(f\"Looking for a relevant cohort directory for {trait}...\")\n", "\n", "# Check available cohorts\n", "available_dirs = os.listdir(tcga_root_dir)\n", "print(f\"Available cohorts: {available_dirs}\")\n", "\n", "# Thyroid-related keywords\n", "thyroid_keywords = ['thyroid', 'thca']\n", "\n", "# Look for Thyroid disease-related directories\n", "thyroid_related_dirs = []\n", "for d in available_dirs:\n", " if any(keyword in d.lower() for keyword in thyroid_keywords):\n", " thyroid_related_dirs.append(d)\n", "\n", "print(f\"Thyroid disease-related cohorts: {thyroid_related_dirs}\")\n", "\n", "if not thyroid_related_dirs:\n", " print(f\"No suitable cohort found for {trait}.\")\n", " # Mark the task as completed by recording the unavailability\n", " validate_and_save_cohort_info(\n", " is_final=False,\n", " cohort=\"TCGA\",\n", " info_path=json_path,\n", " is_gene_available=False,\n", " is_trait_available=False\n", " )\n", " # Exit the script early since no suitable cohort was found\n", " selected_cohort = None\n", "else:\n", " # Select the most specific match - in this case it should be TCGA_Thyroid_Cancer_(THCA)\n", " selected_cohort = thyroid_related_dirs[0] # We'll use the first match if multiple exist\n", "\n", "if selected_cohort:\n", " print(f\"Selected cohort: {selected_cohort}\")\n", " \n", " # Get the full path to the selected cohort directory\n", " cohort_dir = os.path.join(tcga_root_dir, selected_cohort)\n", " \n", " # Get the clinical and genetic data file paths\n", " clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir)\n", " \n", " print(f\"Clinical data file: {os.path.basename(clinical_file_path)}\")\n", " print(f\"Genetic data file: {os.path.basename(genetic_file_path)}\")\n", " \n", " # Load the clinical and genetic data\n", " clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\\t')\n", " genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\\t')\n", " \n", " # Print the column names of the clinical data\n", " print(\"\\nClinical data columns:\")\n", " print(clinical_df.columns.tolist())\n", " \n", " # Basic info about the datasets\n", " print(f\"\\nClinical data shape: {clinical_df.shape}\")\n", " print(f\"Genetic data shape: {genetic_df.shape}\")\n" ] }, { "cell_type": "markdown", "id": "f6ce65d9", "metadata": {}, "source": [ "### Step 2: Find Candidate Demographic Features" ] }, { "cell_type": "code", "execution_count": 3, "id": "5d9456e4", "metadata": { "execution": { "iopub.execute_input": "2025-03-25T04:12:09.063742Z", "iopub.status.busy": "2025-03-25T04:12:09.063622Z", "iopub.status.idle": "2025-03-25T04:12:09.075147Z", "shell.execute_reply": "2025-03-25T04:12:09.074791Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Age columns preview:\n", "{'age_at_initial_pathologic_diagnosis': [74, 65, 55, 57, 33], 'days_to_birth': [-27348, -24102, -20361, -21008, -12295]}\n", "Gender columns preview:\n", "{'gender': ['FEMALE', 'MALE', 'MALE', 'MALE', 'FEMALE']}\n" ] } ], "source": [ "# Identify candidate age and gender columns\n", "candidate_age_cols = ['age_at_initial_pathologic_diagnosis', 'days_to_birth']\n", "candidate_gender_cols = ['gender']\n", "\n", "# Load the clinical data file\n", "cohort_dir = os.path.join(tcga_root_dir, 'TCGA_Thyroid_Cancer_(THCA)')\n", "clinical_file_path, _ = tcga_get_relevant_filepaths(cohort_dir)\n", "clinical_df = pd.read_csv(clinical_file_path, sep='\\t', index_col=0)\n", "\n", "# Extract and preview age columns\n", "if candidate_age_cols:\n", " age_preview = {}\n", " for col in candidate_age_cols:\n", " if col in clinical_df.columns:\n", " age_preview[col] = clinical_df[col].head(5).tolist()\n", " print(\"Age columns preview:\")\n", " print(age_preview)\n", "\n", "# Extract and preview gender columns\n", "if candidate_gender_cols:\n", " gender_preview = {}\n", " for col in candidate_gender_cols:\n", " if col in clinical_df.columns:\n", " gender_preview[col] = clinical_df[col].head(5).tolist()\n", " print(\"Gender columns preview:\")\n", " print(gender_preview)\n" ] }, { "cell_type": "markdown", "id": "bc983fd6", "metadata": {}, "source": [ "### Step 3: Select Demographic Features" ] }, { "cell_type": "code", "execution_count": 4, "id": "7f6950f3", "metadata": { "execution": { "iopub.execute_input": "2025-03-25T04:12:09.076294Z", "iopub.status.busy": "2025-03-25T04:12:09.076182Z", "iopub.status.idle": "2025-03-25T04:12:09.078528Z", "shell.execute_reply": "2025-03-25T04:12:09.078207Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Selected age column: age_at_initial_pathologic_diagnosis\n", "Selected gender column: gender\n" ] } ], "source": [ "# 1. Select age and gender columns based on the preview data\n", "# Inspecting the age columns\n", "# Both 'age_at_initial_pathologic_diagnosis' and 'days_to_birth' have valid values\n", "# 'age_at_initial_pathologic_diagnosis' is directly in years, which is more intuitive\n", "# 'days_to_birth' is negative, representing days before birth (would need conversion)\n", "age_col = 'age_at_initial_pathologic_diagnosis'\n", "\n", "# Inspecting the gender columns\n", "# The 'gender' column has clear 'MALE' and 'FEMALE' values\n", "gender_col = 'gender'\n", "\n", "# 2. Print information about chosen columns\n", "print(f\"Selected age column: {age_col}\")\n", "print(f\"Selected gender column: {gender_col}\")\n" ] }, { "cell_type": "markdown", "id": "678b6bde", "metadata": {}, "source": [ "### Step 4: Feature Engineering and Validation" ] }, { "cell_type": "code", "execution_count": 5, "id": "6a353014", "metadata": { "execution": { "iopub.execute_input": "2025-03-25T04:12:09.079648Z", "iopub.status.busy": "2025-03-25T04:12:09.079539Z", "iopub.status.idle": "2025-03-25T04:13:11.049711Z", "shell.execute_reply": "2025-03-25T04:13:11.049377Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Clinical features (first 5 rows):\n", " Thyroid_Cancer Age Gender\n", "sampleID \n", "TCGA-4C-A93U-01 1 74 0\n", "TCGA-BJ-A0YZ-01 1 65 1\n", "TCGA-BJ-A0Z0-01 1 55 1\n", "TCGA-BJ-A0Z2-01 1 57 1\n", "TCGA-BJ-A0Z3-01 1 33 0\n", "\n", "Processing gene expression data...\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Original gene data shape: (20530, 572)\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Attempting to normalize gene symbols...\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Gene data shape after normalization: (19848, 572)\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Gene data saved to: ../../output/preprocess/Thyroid_Cancer/gene_data/TCGA.csv\n", "\n", "Linking clinical and genetic data...\n", "Clinical data shape: (580, 3)\n", "Genetic data shape: (19848, 572)\n", "Number of common samples: 572\n", "\n", "Linked data shape: (572, 19851)\n", "Linked data preview (first 5 rows, first few columns):\n", " Thyroid_Cancer Age Gender A1BG A1BG-AS1\n", "TCGA-EM-A3AI-01 1 67 0 -0.404874 0.340917\n", "TCGA-ET-A39M-01 1 34 1 1.816826 1.301417\n", "TCGA-DE-A4MC-01 1 43 0 0.457826 0.791217\n", "TCGA-E8-A414-01 1 45 0 0.065126 1.581317\n", "TCGA-EM-A3OA-01 1 55 0 0.403626 -1.004483\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "\n", "Data shape after handling missing values: (572, 19851)\n", "\n", "Checking for bias in features:\n", "For the feature 'Thyroid_Cancer', the least common label is '0' with 59 occurrences. This represents 10.31% of the dataset.\n", "The distribution of the feature 'Thyroid_Cancer' in this dataset is fine.\n", "\n", "Quartiles for 'Age':\n", " 25%: 34.0\n", " 50% (Median): 46.0\n", " 75%: 58.0\n", "Min: 15\n", "Max: 89\n", "The distribution of the feature 'Age' in this dataset is fine.\n", "\n", "For the feature 'Gender', the least common label is '1' with 157 occurrences. This represents 27.45% of the dataset.\n", "The distribution of the feature 'Gender' in this dataset is fine.\n", "\n", "\n", "Performing final validation...\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Linked data saved to: ../../output/preprocess/Thyroid_Cancer/TCGA.csv\n", "Clinical data saved to: ../../output/preprocess/Thyroid_Cancer/clinical_data/TCGA.csv\n" ] } ], "source": [ "# 1. Extract and standardize clinical features\n", "# Use tcga_select_clinical_features which will automatically create the trait variable and add age/gender if provided\n", "# Use the correct cohort identified in Step 1\n", "cohort_dir = os.path.join(tcga_root_dir, 'TCGA_Thyroid_Cancer_(THCA)')\n", "clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir)\n", "\n", "# Load the clinical data if not already loaded\n", "clinical_df = pd.read_csv(clinical_file_path, sep='\\t', index_col=0)\n", "\n", "linked_clinical_df = tcga_select_clinical_features(\n", " clinical_df, \n", " trait=trait, \n", " age_col=age_col, \n", " gender_col=gender_col\n", ")\n", "\n", "# Print preview of clinical features\n", "print(\"Clinical features (first 5 rows):\")\n", "print(linked_clinical_df.head())\n", "\n", "# 2. Process gene expression data\n", "print(\"\\nProcessing gene expression data...\")\n", "# Load genetic data from the same cohort directory\n", "genetic_df = pd.read_csv(genetic_file_path, sep='\\t', index_col=0)\n", "\n", "# Check gene data shape\n", "print(f\"Original gene data shape: {genetic_df.shape}\")\n", "\n", "# Save a version of the gene data before normalization (as a backup)\n", "os.makedirs(os.path.dirname(out_gene_data_file), exist_ok=True)\n", "genetic_df.to_csv(out_gene_data_file.replace('.csv', '_original.csv'))\n", "\n", "# We need to transpose genetic data so genes are rows and samples are columns for normalization\n", "gene_df_for_norm = genetic_df.copy() # Keep original orientation for now\n", "\n", "# Try to normalize gene symbols - adding debug output to understand what's happening\n", "print(\"Attempting to normalize gene symbols...\")\n", "try:\n", " # First check if we need to transpose based on the data format\n", " # In TCGA data, typically genes are rows and samples are columns\n", " if gene_df_for_norm.shape[0] > gene_df_for_norm.shape[1]:\n", " # More rows than columns, likely genes are rows already\n", " normalized_gene_df = normalize_gene_symbols_in_index(gene_df_for_norm)\n", " else:\n", " # Need to transpose first\n", " normalized_gene_df = normalize_gene_symbols_in_index(gene_df_for_norm.T)\n", " \n", " print(f\"Gene data shape after normalization: {normalized_gene_df.shape}\")\n", " \n", " # Check if normalization returned empty DataFrame\n", " if normalized_gene_df.shape[0] == 0:\n", " print(\"WARNING: Gene symbol normalization returned an empty DataFrame.\")\n", " print(\"Using original gene data instead of normalized data.\")\n", " # Use original data\n", " normalized_gene_df = genetic_df\n", " \n", "except Exception as e:\n", " print(f\"Error during gene symbol normalization: {e}\")\n", " print(\"Using original gene data instead.\")\n", " normalized_gene_df = genetic_df\n", "\n", "# Save gene data\n", "normalized_gene_df.to_csv(out_gene_data_file)\n", "print(f\"Gene data saved to: {out_gene_data_file}\")\n", "\n", "# 3. Link clinical and genetic data\n", "# TCGA data uses the same sample IDs in both datasets\n", "print(\"\\nLinking clinical and genetic data...\")\n", "print(f\"Clinical data shape: {linked_clinical_df.shape}\")\n", "print(f\"Genetic data shape: {normalized_gene_df.shape}\")\n", "\n", "# Find common samples between clinical and genetic data\n", "# In TCGA, samples are typically columns in the gene data and index in the clinical data\n", "common_samples = set(linked_clinical_df.index).intersection(set(normalized_gene_df.columns))\n", "print(f\"Number of common samples: {len(common_samples)}\")\n", "\n", "if len(common_samples) == 0:\n", " print(\"ERROR: No common samples found between clinical and genetic data.\")\n", " # Try the alternative orientation\n", " common_samples = set(linked_clinical_df.index).intersection(set(normalized_gene_df.index))\n", " print(f\"Checking alternative orientation: {len(common_samples)} common samples found.\")\n", " \n", " if len(common_samples) == 0:\n", " # Use is_final=False mode which doesn't require df and is_biased\n", " validate_and_save_cohort_info(\n", " is_final=False,\n", " cohort=\"TCGA\",\n", " info_path=json_path,\n", " is_gene_available=True,\n", " is_trait_available=True\n", " )\n", " print(\"The dataset was determined to be unusable for this trait due to no common samples. No data files were saved.\")\n", "else:\n", " # Filter clinical data to only include common samples\n", " linked_clinical_df = linked_clinical_df.loc[list(common_samples)]\n", " \n", " # Create linked data by merging\n", " linked_data = pd.concat([linked_clinical_df, normalized_gene_df[list(common_samples)].T], axis=1)\n", " \n", " print(f\"\\nLinked data shape: {linked_data.shape}\")\n", " print(\"Linked data preview (first 5 rows, first few columns):\")\n", " display_cols = [trait, 'Age', 'Gender'] + list(linked_data.columns[3:5])\n", " print(linked_data[display_cols].head())\n", " \n", " # 4. Handle missing values\n", " linked_data = handle_missing_values(linked_data, trait)\n", " print(f\"\\nData shape after handling missing values: {linked_data.shape}\")\n", " \n", " # 5. Check for bias in features\n", " print(\"\\nChecking for bias in features:\")\n", " is_trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)\n", " \n", " # 6. Validate and save cohort info\n", " print(\"\\nPerforming final validation...\")\n", " is_usable = validate_and_save_cohort_info(\n", " is_final=True,\n", " cohort=\"TCGA\",\n", " info_path=json_path,\n", " is_gene_available=len(linked_data.columns) > 3, # More than just trait/age/gender columns\n", " is_trait_available=trait in linked_data.columns,\n", " is_biased=is_trait_biased,\n", " df=linked_data,\n", " note=\"Data from TCGA Thyroid Cancer cohort used for thyroid cancer analysis.\"\n", " )\n", " \n", " # 7. Save linked data if usable\n", " if is_usable:\n", " os.makedirs(os.path.dirname(out_data_file), exist_ok=True)\n", " linked_data.to_csv(out_data_file)\n", " print(f\"Linked data saved to: {out_data_file}\")\n", " \n", " # Also save clinical data separately\n", " os.makedirs(os.path.dirname(out_clinical_data_file), exist_ok=True)\n", " clinical_columns = [col for col in linked_data.columns if col in [trait, 'Age', 'Gender']]\n", " linked_data[clinical_columns].to_csv(out_clinical_data_file)\n", " print(f\"Clinical data saved to: {out_clinical_data_file}\")\n", " else:\n", " print(\"The dataset was determined to be unusable for this trait. No data files were saved.\")" ] } ], "metadata": { "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.10.16" } }, "nbformat": 4, "nbformat_minor": 5 }