Mutect2
Call somatic short mutations (SNVs and indels) via local assembly of haplotypes using a Bayesian somatic genotyping model and the assembly-based machinery of HaplotypeCaller.
What it does
Call somatic short mutations (SNVs and indels) via local assembly of haplotypes using a Bayesian somatic genotyping model and the assembly-based machinery of HaplotypeCaller. Supports tumor-normal, tumor-only, mitochondrial, and force-calling modes, including joint analysis of multiple samples.
- Somatic short mutation calling
- SNV and indel detection
- Mitochondrial variant calling
- Somatic mosaicism detection
- Category
- Healthcare data and research
- Users
- Genomic researchers, Bioinformatics teams, Cancer genomics researchers
- Public API
- Not offered
- Deployment
- Self-hosted
Not yet disclosed: platforms, languages and support channels.
Pricing
Pricing isn't published
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Security and compliance
No security details published yet
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