byoo's repositories
denovogear
A program to detect denovo-variants using next-generation sequencing data. (http://www.nature.com/nmeth/journal/v10/n10/full/nmeth.2611.html)
HiFi-somatic-WDL
Tumor-normal variant calling workflow using HiFi reads
Language:WDLBSD-3-Clause-Clear000
nanopore-scripts
Various scripts and recipes for working with nanopore data
PEAR
Pair-End AssembeR
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STAAR
An R package for performing STAAR procedure in whole-genome sequencing studies
Language:C++GPL-3.0000
STAARpipeline-Tutorial
The tutorial for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline and STAARpipelineSummary
Language:RGPL-3.0000