SEQanswers

Go Back   SEQanswers > Bioinformatics > Bioinformatics



Similar Threads
Thread Thread Starter Forum Replies Last Post
Live webinar on DNA-Seq Data Analysis - Selected Case Studies on 22 Feb 2017 Strandlife Webinar Series 1 02-20-2017 10:50 PM
Webinar: Achieving Highly Accurate NGS Variant Calling DNASTAR Events / Conferences 0 10-20-2015 05:41 AM
Live webinar Tue Aug 25: MetaSV - An accurate & integrative structura variant caller jenny.hsu Events / Conferences 0 08-14-2015 01:59 PM
modENCODE Data Access Webinar Apr 5th 2012 modencoder Events / Conferences 0 03-21-2012 08:20 AM

Reply
 
Thread Tools
Old 04-17-2017, 03:05 AM   #1
Strandlife
Member
 
Location: All over the world

Join Date: May 2013
Posts: 41
Default Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017

Presenting Strand NGS v3.0 best-practices: a DNA-Seq 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. This live webinar will also cover 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
Hurry.. Register at http://www.strand-ngs.com/webinar_registration
Strandlife is offline   Reply With Quote
Reply

Tags
dna-seq, ngs data analysis, strand ngs, variant calling, webinar

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off




All times are GMT -8. The time now is 11:55 PM.


Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2017, vBulletin Solutions, Inc.
Single Sign On provided by vBSSO