News:Webinar on fast and accurate DNA variant calling on 26 Apr 2017

Question

[Genomics]

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

Answer 1

[Genomics]

Reminder! Register to webinar on Fast and Accurate Variant Calling in #StrandNGS 3.0 at http://www.strand-ngs.com/webinar_registration

Answer 2

[Genomics]

In case you missed this webinar, you can access the webinar recording here http://www.strand-ngs.com/learn/webinar-recordings