First of all, I wish you a prosperous 2018 along with happiness and health for you and your loved ones. This next year comes with lots of anticipation. We at Golden Helix are looking forward to another year of growth and innovation.
Over the last few years, we were able to build a large following of clients in the clinical space. As next-gen sequencing becomes widely adopted, our powerful clinical stack has had significant adoption on a global basis. Our filtering and annotation engine, VarSeq, initially designed to interpret single nucleotide variations, is now able to analyze copy number variations in conjunction with our new product VS-CNV. This is a game changer for many labs as we can simplify the clinical workflow significantly by reducing or even eliminating the need for confirmatory methods such as multiplex ligation-dependent probe amplification or chromosomal microarrays. Some of our customers and collaborators were able to create astonishing results which I will share with you separately. We have also just recently made this capability available in SVS. This means our research centric clients are now able to conduct CNV analysis on NGS data as well.
Read the full story on Our 2 SNPs… here.
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