Join our Life Science Networking Event at the first Tuesday of every month!
The ever-increasing volume of genomic data and the corresponding literature can be hard to keep pace with, making variant interpretation a bottleneck step in the clinical report pipeline. As larger panels, WES, and WGS are ordered more regularly this leads to an influx in the number of variants that may require human assessment. The utilization of a comprehensive database of published variants and accompanying evidence annotations can significantly expedite interpretation, standardize calls between curations and laboratories, and bolster accuracy, adhering to our highest curation standards.
Join us for our next live webinar where we’ll welcome two of our variant curation experts and our Customer Success Manager to explain how Mastermind helps clinical labs handle this increased volume and complexity of genomic information.
You Will Learn: