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
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
The Ebola epidemic in West Africa has proven to be a devastating reminder that humans...
How Accurate Is Your Variant Caller?
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
In the past decade, the ability to determine complex mechanisms underlying disease has been made...
Q&A With Dr. Sheldon Garrison of Promentis Pharmaceuticals
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
Nephropath™ incorporates DNASTAR pipeline for validating processes against NIST “gold standard.” The resources provided by...
Q&A with Dr. Luke Daum of Longhorn Vaccines and Diagnostics
We chatted with Dr. Luke Daum, Chief Scientific Officer at Longhorn Vaccines and Diagnostics about...
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