Genalice Information

Genalice develops software solutions for researchers and clinicians to do read alignment and variant calling on NGS data sets. Using just commodity hardware, users can analyse their data ultra-fast (full genome less than 20 min.) and reach significant storage-footprint reductions, while maintaining or surpassing industry standard accuracy rates. With the exact same signature, Genalice offers solutions for population-calling, trio analysis, somatic-calling and copy number variation calling. Our solutions enable users to process NGS big data in a scalable way and meet the turn-around-times and budgets required for clinical use of NGS.