Síguenos ...

  • Twitter FacebbokFlickrYouTube CESGA

Servizos PYME's

  • Servicios para Empresas

díxitos Decembro

  • díxitos Decembro 2017




Versións dispoñibles:


  • 1.0


multiSNV is a tool for calling somatic single-nucleotide variants (SNVs) using NGS data from a normal and multiple tumour samples of the same patient. Instead of performing multiple pairwise analyses of a single tumour sample and its matched normal, multiSNV jointly considers all available samples under a Bayesian framework to increase sensitivity of calling shared SNVs. multiSNV accepts BAM files (one BAM file for each sample) and produces a single VCF file with variant predictions for all samples.

Guía de uso

Please use the following module commands:

module av multisnv

Check the multisnv available versions

module help multisnv

Get a brief server specific user guide

module load multisnv

Load default version environment

module load multisnv/<version>

Load specific version environment

URL Manual


Ante calquera dúbida ou problema co uso deste paquete de software diríxase a aplicacions@cesga.es