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SNAF

Splicing Neo Antigen Finder (SNAF) is an easy-to-use Python package to identify splicing-derived tumor neoantigens from RNA sequencing data, it can predict, prioritize and visualize MHC-bound neoantigen for T cell (T antigen) and altered surface protein for B cell (B antigen).

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Tutorial and documentation

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Input and Output

Simply put, user needs to supply a folder with bam files, and the HLA type assciated with each patient (using your favorite HLA typing tool). And it will generate predicted immunogenic MHC-bound peptides and altered surface protein. Moreover, there's a myriad of convenient function that enables users to conduct survival analysis, association analysis and publication-quality visualiztion. Check our tutorials for more detail.

Citation

Guangyuan Li, Nathan Salomonis. SNAF: Accurate and compatible computational framework for identifying splicing derived neoantigens [abstract]. Cancer Res 2022;82(12_Suppl)

A preprint will be released soon.

Contact

Guangyuan(Frank) Li

Email: li2g2@mail.uc.edu

PhD student, Biomedical Informatics

Cincinnati Children’s Hospital Medical Center(CCHMC)

University of Cincinnati, College of Medicine

Metadata

Release files for SNAF 0.7.0

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Source distribution for SNAF 0.7.0
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Table of built distributions (wheels) for SNAF 0.7.0
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SNAF-0.7.0-py3-none-any.whl Python 3 none any Details for SNAF-0.7.0-py3-none-any.whl

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