Webinar of the Month | Feb 2018


Webinar on RNA-Seq Data Analysis by Dr. Suman Kapoor, Manager- Application Science on 28 Feb

Strand NGS is a biologist friendly NGS analysis tool that allows biologists to analyze their data using a very intuitive workflow for the analysis and visualization of RNA-Seq data. This webinar will give an overview of the workflow which includes Transcriptome/ Genome alignment, Differential expression analysis, Splicing events and gene fusion detection. Strand NGS also supports novel discovery like identification of novel genes, exons and novel splice junctions.

We will highlight the use of Strand NGS features such as PCA, sample correlation, clustering, Venn diagrams, CVA, UMI support and elastic genome browser used in RNA-Seq workflow that supports large scale RNA-Seq data analysis too. The tool also supports biological contextualization on the set of interesting genes from the data by allowing downstream analysis such as GO and pathway analysis. The product has an option to create pipelines for time consuming jobs which automates analysis and leaves more time for end data interpretation. This webinar will give an overview of the features in the RNA-Seq data analysis workflow in Strand NGS.

Webinar details

Sessions San Francisco Time
(PST)
Tokyo Time
(JST)
Berlin Time
(CET)
Mumbai Time
(IST)
Session 1 28 Feb
12:00 AM
28 Feb
05:00 PM
28 Feb
09:00 AM
28 Feb
01:30 PM
Session 2 28 Feb
08:00 AM
1 Mar
01:00 AM
28 Feb
05:00 PM
28 Feb
09:30 PM

Hurry! Registrations to this webinar will close at 7 AM PST, 28 Feb 2018.

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