The bottleneck for genomic insights is the computational analysis that follows sequencing. It’s the process of detecting key markers and outliers, called variants, in the genetic data.
Brytlyt can reduce the processing time from days to seconds.
Whole genome sequencing and analysis demand is rising, and the data generated is doubling almost every year.
Brytlyt’s GPU database can massively accelerate the work medical professionals do, identifying mutations and variants in the data.
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