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DRIVE: database of drug-induced transcriptomic response, alternative splicing, and splicing-derived neoantigens in cancer cell lines

Although drugs, alternative splicing, and neoantigens are intimately interconnected, existing resources fail to integrate these three dimensions. To bridge this gap, we constructed DRIVE (Drug-induced RNA profile, Isoform Variability and Epitopes), a comprehensive resource integrating, drug induced transcriptomic responses, alternative splicing and neoantigen landscapes. We systematically retrieved drug-treated and matched control cancer cell line transcriptomic datasets from the GEO database, utilizing Large Language Models (LLMs) combined with rigorous manual inspection to ensure high-fidelity metadata. By implementing a standardized pipeline for raw data processing, we quantified drug-induced differential gene expression, AS alterations, and predicted splice-neoantigens across thousands of conditions. The Shiny Web server is available at https://componclab.com/DRIVE

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Contents

This repository contains code for the processing pipeline of raw data, reproducible data, code, and analysis reports for the main results in the paper, as well as code for building the DRIVE Shiny App.

  1. Processing pipeline of raw data
  2. Shiny Web app: Code and resource for building Shiny app.
  3. The data for analysis in manuscript and shiny app is available in Zenodo with DOI: 10.5281/zenodo.19816802. Important files include:
  • Metadata file: data/all_sample_meta.rds
  • Deseq results: ××_deseq.rds in scripts/Shiny/data/
  • rMats results: ××_rmats.rds in scripts/Shiny/data/
  • HLA binding peptides prediction: ××_binding_pep.rds and ××_binding_pep_meta.rds in scripts/Shiny/data/
  1. The analysis report the reproducibility of the manuscript results can be view online in https://comonclab.github.io/DRIVE/

Citation

Wu, T., Tang, H.-F., and Wang, W. (2026). DRIVE: a comprehensive resource deciphering drug-induced transcriptomic and splicing response in cancer cell. Neoplasia 79, 101336. https://doi.org/10.1016/j.neo.2026.101336.

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a comprehensive resource deciphering drug-induced transcriptomic response, alternative splicing, and splicing-derived neoantigens in cancer cell lines

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