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MuSE
Somatic point mutation caller for tumor-normal paired samples in next-generation sequencing data, based on the F81 Markov substitution model for molecular evolution with a sampl...
What is MuSE?
Somatic point mutation caller for tumor-normal paired samples in next-generation sequencing data, based on the F81 Markov substitution model for molecular evolution with a sample-specific error model. Version 2.0 features parallel computing for 50-60x speedup and supports WES and WGS data.
Product typeScientific Models
Pricing ·
DeploymentSelf-hosted
APINot available
What teams use MuSE for
Somatic point mutation calling in tumor-normal paired NGS data
Cancer genomic research variant detection
Consensus variant calling strategies in pan-cancer studies
Integrations and access
Platforms, integrations, and language support vary by plan and region. Confirm final requirements with the vendor.
Platforms
IntegrationsAPI and webhooks
Languages
Support
What reviewers say
Community reviewsReviews are owned and editable by their authors.
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Enterprise readiness
Compliance claims are normalized from current vendor documentation and independently reviewed by SOTA2.
Data retention:
Benchmarks and comparisons
Independent benchmarksStructured task results are being verified.
Side-by-side comparisonsComparison workspaces will be available in a later release.
