script for variant calling of RNA-Seq
script for variant calling of Exome-Seq
CusVarDB generated variant protein database from NGS-datasets
SNP calling, annotation and gene/transcripts expression quantification
Bisulfite-seq/NOMe-seq SNPs & cytosine methylation caller
Pure java NGS mapping soft run on Hadoop 2.0
THIS REPOSITORY HAS BEEN MOVED TO GITHUB
MIP VARiant calling tool
NGS compute distro proloaded with pipeline analysis software
A set of tools for working with high-throughput sequencing data
QC for variant discovery from next gen sequence in pedigrees
Copy number variation (CNV) detection in exome sequencing data
Plots allele balance histogram and assesses sample contamination.
Bisulfite-seq/NOMe-seq SNPs & cytosine methylation caller