Pinned Repositories
Haloplex
loci_specific_coverage
deepvariant
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
ngs-bits
Short-read sequencing tools
AnnotSV
Annotation and Ranking of Structural Variation
cutadapt
Cutadapt removes adapter sequences from sequencing reads
SeeNV
bcftools
This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html
doc-ANNOVAR
Documentation for the ANNOVAR software