Exome
CoNIFER 0.2.2 Beta v.1.0
CoNIFER uses exome sequencing data to find copy number variants (CNVs) and genotype the copy-number of duplicated genes.
SNVer v.0.0.2
Detection of rare and common variants in next generation sequencing. SNVer call common and rare variants in the analysis of pool or individual next-generation sequencing data. The software reports one single overall p-value for evaluating the