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díxitos Xulio 2018

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Aplicacións

multisnv

Versións dispoñibles:

FinisTerraeII

  • 1.0
  • 2.3

Descrición


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


Soporte


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