PRP: Pathogenic Risk Prediction for Rare Nonsynonymous Single Nucleotide Variants
收藏Zenodo2025-04-11 更新2026-05-26 收录
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https://zenodo.org/doi/10.5281/zenodo.15195285
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资源简介:
This repository contains the training dataset and three independent test datasets used in the study "PRP:Pathogenic Risk Prediction for Rare Nonsynonymous Single Nucleotide Variants."
Each file includes the following columns:
chr: chromosome
pos: genomic position
alRef: Reference allele
alAlt: Alternative allele
aaRef: Reference amino acid
aaAlt: Altered amino acid
clnSig: Clinical significance of the variant (pathogenic=1, benign=0)
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Zenodo创建时间:
2025-04-11



