There are 0 repository under varscan topic.
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
accessory scripts for processing varscan somatic/copynumber outputs.
Pipeline of somatic variant analysis using Waldenstrom macroglobulinemia patient’s RNA-seq data, including tools like STAR, HTseq, VarScan in parallel computing in SGE clusters, Deseq2 and GSEA in R
software for processing tuberculosis whole genome data. interface to the BWA, VarScan, SamTools etc.