product foundation

We are currently building enterprise-class software for next generation sequencing data analysis based on our SLIM Search™ sequence comparison technology.  This foundation supports read mapping and alignment functions with unique speed, accuracy and mismatch tolerance.  In either Linux (Java) or Windows (.NET) environments, this software can reduce processing requirements for read mapping and alignment of short-read data by an order of magnitude. 

SLIM Search is highly tolerant of mismatches such as indels and substitutions.  This makes it well suited to address challenging problems such as SNP discovery during disease investigation, where millions of reads must be accurately mapped against the full human genome.  Additionally, mismatch tolerance adds valuable sensitivity to other analysis applications like gene expression, comparative genomics and metagenomics.  

Our initial product release will deliver robust, flexible software that satisfies the operational efficiency requirements of large-scale multi-core data center environments.  Early access to this product with additional advisory services and community engagement is available now.