A lightweight and modular toolkit for rapid preprocessing of clinical and molecular datasets.
clinomics-toolkit is designed as a collection of reusable utilities for cleaning, validating, transforming, and preparing biomedical tabular data for downstream machine learning, statistical analysis, and exploratory workflows.
The project aims to provide simple, composable, and analysis-oriented preprocessing functions that can be easily integrated into research pipelines, prototype analyses, and multi-omics workflows.
- Clinical data preprocessing
- Column name standardization
- Missing value imputation
- Categorical variable encoding
- Expression-like data transformation
- Z-score normalization
- Low-variance feature filtering
- Sample alignment checks
- Lightweight R utilities for expression-style normalization
Clone the repository:
git clone https://github.com/YOUR_USERNAME/clinomics-toolkit.git
cd clinomics-toolkitpip install -e ".[dev]"import pandas as pd
from clinomics_toolkit.preprocessing import clean_column_names
from clinomics_toolkit.normalization import log_transform, zscore_normalize
from clinomics_toolkit.clinical import encode_categorical_variables
df = pd.DataFrame({
"Patient ID": ["P1", "P2", "P3"],
"Age at Onset": [12, 24, 31],
"Sex": ["F", "M", "F"],
"Gene A": [10, 25, 50],
})
df = clean_column_names(df)
clinical = encode_categorical_variables(
df[["age_at_onset", "sex"]],
columns=["sex"]
)
features = log_transform(df[["gene_a"]])
features = zscore_normalize(features)pytest tests/or:
bash scripts/run_tests.sh- Core preprocessing utilities
- Basic clinical variable encoding
- Basic normalization tools
- Validation checks
- Demo notebook
- Synthetic biomedical sample dataset
- Multi-omics feature integration utilities
- Documentation website
- CI with GitHub Actions
MIT License.