Annotate, Filter and Report CNVs with InHelix | GenomeWeb
July 12, 2016
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Annotate, Filter and Report CNVs with InHelix

Partner Webinar

Dr. Peter Schols is the founder and CEO of Diploid, a company dedicated to providing world class solutions for rare disease diagnostics.

InHelix is software for annotating, visualizing and reporting CNVs obtained from NGS, with a focus on rare disease diagnostics. With its unique features such as live filtering, intelligent CNV prioritization and integration of phenotype data, InHelix provides a new, efficient and user-friendly solution for CNV analysis.


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