Tag Archives: Germline Workflow

Reporting Secondary Germline Variants in VSClinical AMP

         March 2, 2022
Reporting Secondary Germline Variants in VSClinical AMP

Tumor profiling via next generation sequencing (NGS) often reveals secondary germline variants that may constitute important incidental findings. In May 2021, the American College of Medical Genetics and Genomics (ACMG) released an updated policy statement for reporting incidental findings in exome and genome sequencing data along with a corresponding list of genes. These recommendations state that laboratories should report pathogenic… Read more »

Upcoming Webcast: Using Varseq Templates to Advance and Customize Variant Analysis

         March 23, 2020

Golden Helix ships a variety of templates that are designed to provide a starting point for users to evaluate variants in VarSeq. Naturally, as users become more familiar with the software, there is a desire and necessity to tailor the template design to accommodate a more thorough variant analysis. To add to these template customizations there are several algorithms and… Read more »