Upcoming webinar – RNA-Seq data analysis


Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical approach and Splicing events detection. Strand NGS also supports novel discovery like identification of novel genes, exons and Novel splice junctions, alongside it can also detect gene fusion events. Further downstream analysis such as GO and pathway analysis can be performed on the set of interesting genes. 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 and also highlights on parameters within each feature that can be optimized depending on datasets and analysis needs.

Webinar Details

Sessions San Francisco Time
Tokyo Time
Berlin Time
Mumbai Time
Session 1 9 Nov
1:00 AM
9 Nov
6:00 PM
9 Nov
10:00 AM
9 Nov
2:30 PM
Session 2 9 Nov
9:00 AM
10 Nov
2:00 AM
9 Nov
6:00 PM
9 Nov
10:30 PM

About Speaker

Mr. Sugandan Sivamani, Senior Application Scientist, Strand Life Sciences, has over 9 years experience in analysing Genomics data (NGS and Microarrays). Sugandan, holds a master degree in Bioinformatics. His interest is mainly in Genomics applications, Bioinformatics and Product Management. Prior to joining the Strand NGS team, he was working with the GeneSpring team, a multi-omics analysis software for Microarrays data analysis.
Email: sales@strandngs.com
Phone (USA): 1-800-752-9122
Phone (Worldwide): +1-650-353-5060
Email: support@strandngs.com
Phone (USA): 1-800-516-5181
Phone (Worldwide): +1-650-288-4559

Leave a Reply

Your email address will not be published. Required fields are marked *


Time limit is exhausted. Please reload CAPTCHA.