CoCoRV: a rare variant analysis framework using publicly available genotype summary counts to prioritize germline disease-predisposition genes
Wenan Chen, Shuoguo Wang, Saima Sultana Tithi, David W. Ellison, Gang Wu
CoCoRV prioritizes germline disease-predisposition genes by using public genotype summary counts as controls, effectively identifying cancer-predisposition genes in pediatric cancer cohorts.
bioRxiv · Sep 29, 2021 · PreprintGenetics