Targeted Analysis of sequence Reads for GenoTyping of HLA/MHC genes
This script extracts 16S rRNA sequences from multifasta files
Script for fusion detection in DNAseq and RNAseq
Fitting Y chromosome haplogroups by maximum likelihood
SNP calling, annotation and gene/transcripts expression quantification
Comparative analysis of haploid next-generation genome sequence data
Tools for genomic analysis
Variant detection in next-generation sequencing data
A tool for misalignment filtration on SAM-format sequences with SVM
Bacterial Intergenic Region Analysis Pipeline
NGS compute distro proloaded with pipeline analysis software
a simple and rapid method for genome-wide SNP and methylation site
SOAPindel2 focusing on calling indels from the next-generation p
estimating Multiplicity Of Infection using short read sequence data
Find Microsatellites in a ".vcf" report
NGS analysis tool
Gaea is designed for re-sequencing tasks.