p3/preprocess/Retinoblastoma/code/GSE29686.py

# Path Configuration
from tools.preprocess import *

# Processing context
trait = "Retinoblastoma"
cohort = "GSE29686"

# Input paths
in_trait_dir = "../DATA/GEO/Retinoblastoma"
in_cohort_dir = "../DATA/GEO/Retinoblastoma/GSE29686"

# Output paths
out_data_file = "./output/preprocess/3/Retinoblastoma/GSE29686.csv"
out_gene_data_file = "./output/preprocess/3/Retinoblastoma/gene_data/GSE29686.csv"
out_clinical_data_file = "./output/preprocess/3/Retinoblastoma/clinical_data/GSE29686.csv"
json_path = "./output/preprocess/3/Retinoblastoma/cohort_info.json"

# Get file paths
soft_file_path, matrix_file_path = geo_get_relevant_filepaths(in_cohort_dir)

# Get background info and clinical data
background_info, clinical_data = get_background_and_clinical_data(matrix_file_path)
print("Background Information:")
print(background_info)
print("\nSample Characteristics:")

# Get dictionary of unique values per row 
unique_values_dict = get_unique_values_by_row(clinical_data)
for row, values in unique_values_dict.items():
    print(f"\n{row}:")
    print(values)
# 1. Gene Expression Data Availability
# Based on series title and design, this appears to be a gene expression study of retinoblastoma
is_gene_available = True

# 2.1 Data Availability
# From sample characteristics, only cell type information is available
# All samples are retinoblastoma (tumor/cell line) vs normal is implied
trait_row = 0  # Using cell type row to determine tumor status
age_row = None # Age not available  
gender_row = None # Gender not available

# 2.2 Data Type Conversion Functions
def convert_trait(x):
    """Convert cell type to binary: 1 for tumor/cell line, 0 for normal"""
    if pd.isna(x):
        return None
    value = x.split(': ')[1].lower() if ': ' in x else x.lower()
    # All samples appear to be tumor/cell line based on characteristics
    return 1

def convert_age(x):
    return None  # Not available

def convert_gender(x):
    return None  # Not available

# 3. Save metadata
is_trait_available = trait_row is not None
validate_and_save_cohort_info(is_final=False, 
                            cohort=cohort,
                            info_path=json_path,
                            is_gene_available=is_gene_available,
                            is_trait_available=is_trait_available)

# 4. Clinical Feature Extraction
clinical_features = geo_select_clinical_features(
    clinical_df=clinical_data,
    trait=trait,
    trait_row=trait_row,
    convert_trait=convert_trait,
    age_row=age_row,
    convert_age=convert_age,
    gender_row=gender_row,
    convert_gender=convert_gender
)

# Preview and save clinical features
print("Clinical Features Preview:")
print(preview_df(clinical_features))
clinical_features.to_csv(out_clinical_data_file)
# Get gene expression data from matrix file
genetic_data = get_genetic_data(matrix_file_path)

# Examine data structure
print("Data structure and head:")
print(genetic_data.head())

print("\nShape:", genetic_data.shape)

print("\nFirst 20 row IDs (gene/probe identifiers):")
print(list(genetic_data.index)[:20])

# Get a few column names to verify sample IDs
print("\nFirst 5 column names:")
print(list(genetic_data.columns)[:5])
# Affymetrix probe IDs need to be mapped to gene symbols
requires_gene_mapping = True
# Extract gene annotation data
gene_annotation = get_gene_annotation(soft_file_path)

# Display column names and preview data
print("Column names:")
print(gene_annotation.columns)

print("\nPreview of gene annotation data:")
print(preview_df(gene_annotation))
# Get gene mapping dataframe from annotation data
# 'ID' column in gene annotation matches probe IDs in expression data
# 'Gene Symbol' column contains the target gene symbols
mapping_data = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Gene Symbol')

# Apply gene mapping to convert probe data to gene expression data
gene_data = apply_gene_mapping(genetic_data, mapping_data)

# Preview the mapped gene data
print("Gene expression data shape after mapping:", gene_data.shape)
print("\nFirst few mapped genes and their expression values:")
print(gene_data.head())
# Reload clinical data that was processed earlier
selected_clinical_df = pd.read_csv(out_clinical_data_file, index_col=0)

# 1. Normalize gene symbols 
gene_data = normalize_gene_symbols_in_index(gene_data)
gene_data.to_csv(out_gene_data_file)

# 2. Link clinical and genetic data
linked_data = geo_link_clinical_genetic_data(selected_clinical_df, gene_data)

# 3. Handle missing values systematically  
linked_data = handle_missing_values(linked_data, trait)

# 4. Check for bias in trait and demographic features
trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)

# 5. Final validation and information saving
note = "Dataset contains gene expression data from primary human retinoblastoma samples profiled with Affymetrix microarray."
is_usable = validate_and_save_cohort_info(
    is_final=True,
    cohort=cohort, 
    info_path=json_path,
    is_gene_available=True,
    is_trait_available=True,
    is_biased=trait_biased,
    df=linked_data,
    note=note
)

# 6. Save linked data only if usable 
if is_usable:
    os.makedirs(os.path.dirname(out_data_file), exist_ok=True)
    linked_data.to_csv(out_data_file)