4 results found Sort:

428
422
mit
134
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Created 2019-04-30
7,940 commits to master branch, last one 2 months ago
38
150
mit
22
Detect and visualize target mutations by scanning FastQ files directly
Created 2016-07-23
259 commits to master branch, last one 3 years ago
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116
mit
13
Generate duplex/single consensus reads to reduce sequencing noises and remove duplications
Created 2018-05-03
112 commits to master branch, last one about a year ago