SEQanswers

SEQanswers (http://seqanswers.com/forums/index.php)
-   Webinar Series (http://seqanswers.com/forums/forumdisplay.php?f=38)
-   -   Webinar on Analysis of Variants using GeneSpring GX 14.9 on 6 Dec 2017 (http://seqanswers.com/forums/showthread.php?t=79239)

Strandlife 11-20-2017 03:21 AM

Webinar on Analysis of Variants using GeneSpring GX 14.9 on 6 Dec 2017
 
Live webinar on Analysis of Variants using GeneSpring GX 14.9 by Dr. Dipa Roy Choudhury on 6 Dec 2017, 8 AM PST
Abstract:
Variant analysis workflow in GeneSpring GX is designed for detection, management and analysis of genetic variants such as single nucleotide polymorphisms (SNPs) and InDels. The webinar showcases SNP data analysis from a public repository for identification of germline and somatic mutations. This is a simple workflow for selection of homozygous SNPs from Variant Call Format (VCF) file and for filtering based on heterozygous SNPs, multi-nucleotide polymorphisms (MNPs) and insertion-deletions (InDels). Multi-omic integration of datasets shows related attributes from different datasets in a biologically meaningful way.
To attend, register here: http://genespring-support.com/support/webinars

Strandlife 11-27-2017 01:31 AM

Hurry... Just 10 days to go for the webinar. Register to attend at http://genespring-support.com/support/webinars


All times are GMT -8. The time now is 04:57 PM.

Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2019, vBulletin Solutions, Inc.