Rapid, Large-Scale Prioritizing of Human Variants with Lasergene Genomics Suite
Lasergene Genomics Suite now includes access to the Variant Annotation Database (VAD) for human sequencing...
DNASTAR LabViews: Blaire Bacher of Orion Genomics
Jun 21, 2016
In this installment of DNASTAR LabViews, we talk with Blaire Bacher of Orion Genomics about her work sequencing...
Dr. Michael Pauly of Mapp Biopharmaceutical on Ebola and ZMapp
Oct 7, 2015
The Ebola epidemic in West Africa has proven to be a devastating reminder that humans...
How Accurate Is Your Variant Caller?
Sep 23, 2015
If you are using Next Generation Sequencing (NGS) for clinical research, cancer genomics, genome-wide association...
Discovery of Gene Candidates from NGS Data Using A Researcher Friendly Pipeline and Filters
Nov 20, 2014
In the past decade, the ability to determine complex mechanisms underlying disease has been made...
Q&A With Dr. Sheldon Garrison of Promentis Pharmaceuticals
Nov 14, 2014
We chatted with Dr. Sheldon Garrison, Director of Pediatric and Rare Diseases at Promentis Pharmaceuticals...
GIAB Use Case: Bringing NA12878 Call Sets to Kidney Disease
Oct 7, 2014
Nephropath™ incorporates DNASTAR pipeline for validating processes against NIST “gold standard.” The resources provided...
Q&A with Dr. Luke Daum of Longhorn Vaccines and Diagnostics
Sep 25, 2014
We chatted with Dr. Luke Daum, Chief Scientific Officer at Longhorn Vaccines and Diagnostics about...
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