Continuing our DNA-Seq webinar series, we’ll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best practices workflow is twice as fast as its GATK counterpart, and results in precision/recall rates of up to 99%/98% on whole exome and whole genome samples. We’ll also speak briefly about some of the other features in v3.0 including one-shot pipelines, TSS plots, RNA-Seq performance improvements, and, for the first time, HGVS notations for SNP effect analysis.
Speaker: Dr. Radhakrishna Bettadapura, or RK, is a Senior Software Engineer at Strand Life Sciences.
Date: 26 Apr 2017, Session 1: 2:30 PM IST; Session 2: 9:30 PM IST