<![CDATA[BOL: April 2017]]> https://bioinformaticsonline.com/news/archive/Yeshodari/1491022800/1493614800? https://bioinformaticsonline.com/news/view/32253/webinar-on-fast-and-accurate-dna-variant-calling-on-26-apr-2017 Fri, 21 Apr 2017 06:14:37 -0500 https://bioinformaticsonline.com/news/view/32253/webinar-on-fast-and-accurate-dna-variant-calling-on-26-apr-2017 <![CDATA[Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017]]> 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.

Register here: http://www.strand-ngs.com/webinar_registration

]]> Yeshodari