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Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Created
2019-04-30
7,534 commits to master branch, last one 25 days ago
Whole Genome Sequencing analysis, WGS analysis
Created
2023-06-25
39 commits to main branch, last one about a year ago
A handy variant calling pipeline generator for whole-genome sequencing (WGS) and whole exom sequencing data (WES) analysis. 一个简易且全面的 WGS/WES 分析流程生成器.
Created
2020-04-08
362 commits to master branch, last one 7 days ago
An R package for performing STAAR procedure in whole-genome sequencing studies
Created
2019-08-10
155 commits to master branch, last one 19 days ago
vcfdist: Accurately benchmarking phased variant calls
Created
2022-03-22
495 commits to master branch, last one 3 months ago
Detect novel (and reference) STR expansions from short-read data
Created
2019-07-09
346 commits to master branch, last one about a year ago
An R package for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline
Created
2021-11-06
138 commits to main branch, last one about a month ago