<![CDATA[BOL: Joint webinar by Agilent Technologies and Strand Life Sciences on 'Analysis of Variants using GeneSpring GX' on 6 Dec]]> https://bioinformaticsonline.com/news/view/34334/joint-webinar-by-agilent-technologies-and-strand-life-sciences-on-analysis-of-variants-using-genespring-gx-on-6-dec? https://bioinformaticsonline.com/news/view/34334/joint-webinar-by-agilent-technologies-and-strand-life-sciences-on-analysis-of-variants-using-genespring-gx-on-6-dec Wed, 15 Nov 2017 06:57:06 -0600 https://bioinformaticsonline.com/news/view/34334/joint-webinar-by-agilent-technologies-and-strand-life-sciences-on-analysis-of-variants-using-genespring-gx-on-6-dec <![CDATA[Joint webinar by Agilent Technologies and Strand Life Sciences on 'Analysis of Variants using GeneSpring GX' on 6 Dec]]> Live webinar on Analysis of Variants using GeneSpring GX 14.9 on 6th Dec at 8 AM PST
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.

Speaker: Dr. Dipa Roy Choudhury, Senior Application Scientist, Agilent Technologies Inc.
Details: December 6, 2017 at 8:00 am PST
Register for this Webinar

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