Webinar: CLC Genomics Workbench epigenomics tools We have revolutionized how epigenomics data is efficiently processed, identified and interpreted, and in...

Human Genome Variation Society (HGVS) is hosting a meeting on "Clinical Interpretation of Variants from Next-Generation Sequencing". The meeting will...

ASM Microbe 2016 is the largest gathering of microbiologists and we'll of course be there to present our microbial genomics solution....

The 11th Sequencing, Finishing and Analysis in the Future (SFAF) annual meeting will be held June 1-3, 2016 in Santa Fe, NM....

Many great papers citing CLC Genomics Workbench have come out just in the last few months. To give you an...

In the past several months, customers have performed remarkable work with CLC Genomics Workbench, a tool that offers customizable bioinformatics...

It’s DNA Day! DNA Day marks two significant DNA-related milestones — the 1953 discovery of DNA’s double helix and the...

Part four of our webinar series on liquid biopsies:Circulating cell-free DNA purification, sequencing and data interpretation Identification and monitoring of cancer...

Our hereditary disease solution performs best in terms of clinical accuracy at the Critical Assessment of Genome Interpretation (CAGI) conference....

New, powerful bioinformatics tool: The RNA-Seq Explorer Solution Today we announced our new RNA-Seq Explorer Solution — a powerful bioinformatics...