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Powerful, Accessible Clinical Genomics

From raw genetic data to answers. 

One step.

One app.

Introducing VelosGT

Discover variants and rare diseases in minutes.
Process whole exomes in 30 min* on a laptop, including automatic
annotation and disease discovery.
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VelosGT accepts fasta/fastq/gz raw data files  

*whole exomes typically take between 15-60 minutes on a 2020 MacBook pro i7

See How It Works

This 6 minute tutorial analyzes three small read files and then performs a trio analysis while giving a brief overview of the tools available.

Meet Your New Tool

VelosGT detects clinically relevant and novel variants present in a genome.  It then automatically displays associated diseases and assesses functional impact.

Rapid, Accurate Results

Our high-performance algorithm processes a whole exome in 15-60min* on an average Mac laptop

*benchmarked on a 2020 MacBook Pro i7 

Single Step Processing

VelosGT performs alignment, variant calling, annotation, and prioritization in one step

More Needles, Less Hay

Variants are automatically annotated and correlated with ClinVar, quickly surfacing pathogenic variants

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