p3/preprocess/Ovarian_Cancer/code/GSE103737.py

# Path Configuration
from tools.preprocess import *

# Processing context
trait = "Ovarian_Cancer"
cohort = "GSE103737"

# Input paths
in_trait_dir = "../DATA/GEO/Ovarian_Cancer"
in_cohort_dir = "../DATA/GEO/Ovarian_Cancer/GSE103737"

# Output paths
out_data_file = "./output/preprocess/3/Ovarian_Cancer/GSE103737.csv"
out_gene_data_file = "./output/preprocess/3/Ovarian_Cancer/gene_data/GSE103737.csv"
out_clinical_data_file = "./output/preprocess/3/Ovarian_Cancer/clinical_data/GSE103737.csv"
json_path = "./output/preprocess/3/Ovarian_Cancer/cohort_info.json"

# Get file paths for SOFT and matrix files
soft_file_path, matrix_file_path = geo_get_relevant_filepaths(in_cohort_dir)

# Get background info and clinical data from the matrix file
background_info, clinical_data = get_background_and_clinical_data(matrix_file_path)

# Create dictionary of unique values for each feature
unique_values_dict = get_unique_values_by_row(clinical_data)

# Print the information
print("Dataset Background Information:")
print(background_info)
print("\nSample Characteristics:")
for feature, values in unique_values_dict.items():
    print(f"\n{feature}:")
    print(values)
# 1. Gene Expression Data Availability
# Based on background info, it contains "genome-wide transcriptome profiling"
is_gene_available = True

# 2.1 Data Row Identification
# Norepinephrine content can be used as trait indicator
trait_row = 5
# Age is available in row 0
age_row = 0
# Gender is not available 
gender_row = None

# 2.2 Data Type Conversion Functions
def convert_trait(x):
    # Extract value after colon and convert norepinephrine binary indicator
    if not isinstance(x, str):
        return None
    value = x.split(":")[-1].strip()
    if value == "0":
        return 0
    elif value == "1": 
        return 1
    return None

def convert_age(x):
    # Extract numeric age value
    if not isinstance(x, str):
        return None
    try:
        age = float(x.split(":")[-1].strip())
        return age
    except:
        return None

def convert_gender(x):
    # Not used since gender data unavailable
    return None

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

# 4. Extract clinical features
if trait_row is not None:
    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 the extracted features
    preview = preview_df(clinical_features)
    print("Preview of clinical features:", preview)
    
    # Save to CSV
    clinical_features.to_csv(out_clinical_data_file)
# Extract genetic data matrix
genetic_data = get_genetic_data(matrix_file_path)

# Print first few rows with column names to examine data structure
print("Data preview:")
print("\nColumn names:")
print(list(genetic_data.columns)[:5])
print("\nFirst 5 rows:")
print(genetic_data.head())
print("\nShape:", genetic_data.shape)

# Verify this is gene expression data and check identifiers
is_gene_available = True

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

# Save gene expression data 
genetic_data.to_csv(out_gene_data_file)
# Based on inspecting the gene identifiers (A1BG, A1CF, etc), these appear to be valid human gene symbols
# so no mapping is needed
requires_gene_mapping = False
# 1. Normalize gene symbols and save gene data
normalized_gene_data = normalize_gene_symbols_in_index(genetic_data)
os.makedirs(os.path.dirname(out_gene_data_file), exist_ok=True)
normalized_gene_data.to_csv(out_gene_data_file)

# 2. Link clinical and genetic data  
clinical_features = pd.read_csv(out_clinical_data_file, index_col=0)
linked_data = geo_link_clinical_genetic_data(clinical_features, normalized_gene_data)

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

# 4. Judge bias in features and remove biased ones
trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)

# 5. Final validation and save metadata
is_usable = validate_and_save_cohort_info(
    is_final=True,
    cohort=cohort,
    info_path=json_path,
    is_gene_available=is_gene_available, 
    is_trait_available=True,
    is_biased=trait_biased,
    df=linked_data,
    note="Gene expression data from 97 ovarian carcinoma samples, examining transcriptional correlates of tissue norepinephrine content."
)

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