As NGS tests become broader and more sophisticated, the task to extract relevant, actionable information and to stay up-to-date with published disease-causing variants becomes increasingly difficult and time-consuming.
Join us for a free 1-hour webinar, where we will show you how to identify disease-relevant genes and variants and how to use contextually relevant information to annotate and prioritize causal variants.
Learn how to:
– Filter/prioritize variants to identify causal variants underlying inherited diseases and traits
– Access trustworthy information of known variants in disease-relevant genes for panel development or assay design
Get connected to the industry’s most comprehensive collection of biological and clinical findings to advance your translational research. Whether you are searching for a “variant needle” in a “NGS data haystack” or need access to trustworthy information about known variants, we have a solution with the depth and breadth you need.
