Webinar: Sourcing multiple databases for NGS variant discovery   Correct identification of actionable variants has always been the most challenging...

RNA-Seq, a path to biological insight Are you getting the most our of your RNA-Seq data from plant, animal, or...

CNV Expert Rajini Haraksingh Studies Human Variation at Stanford, Rare Genomics Institute Rajini Haraksingh aims for a broad understanding of...

Webinar on large-scale NGS testing The webinar is sponsored by Intel and takes place on April 2, 2015, 11 am...

Mar 24th – Mar 28th 2015   The ACMG 2015 Annual Clinical Genetics Meeting – sponsored by the American College...

Webinar Want to learn how to link protein sequence and 3D structure data in CLC workbenches and transfer annotations from...

An overview of the current NGS market Would you like to get an overview of the current NGS market? Our...

Webinar: POSSUMweb, HGMD®, and IVA allow you to combine genetics and morphology information.   This webinar demonstrates how to combine genetics and...

Rare Disease Specialists Identify Novel Pediatric Syndrome in Three Families In the world of rare disease, genomics has been transformational....

We are pleased to announce, in collaboration with 12 other leading life science organizations, the Allele Frequency Community (#AlleleFreq), a landmark initiative...