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

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

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

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…

Advancing NGS data analysis and interpretation: CLC Cancer Research Workbench and Ingenuity Variant Analysis Deep-sequencing technologies enable critical insights into…

Our 2014 survey on the NGS market was completed by 529 respondents and provides a good summary of the current NGS…

We are pleased to announce the latest release of Ingenuity Variant Analysis. New! Enhancements included in this update: Direct Access…

Allele Frequency Community is an expansive, ethnically diverse, freely available community resource for allele frequency annotation Imagine Human Genome Interpretation minus…

In Sickle Cell Project, Baylor Scientist Discovers Link to Fetal Hemoglobin Production When Baylor’s Vivien Sheehan won a grant competition…

Webinar: Practical Application of CLC Cancer Research Workbench and Ingenuity Variant Analysis for NGS data analysis Want to learn how…