[Webinar on RNA-Seq Data Analysis on 28 Feb 2018 by Dr. Suman Kapoor][1] Strand NGS is a biologist friendly NGS analysis tool that allows biologists …

[Live webinar on Unravelling complex mutational events in clinical cases using the power of Next generation sequencing data analysis by Dr Satish Sankaran on 31 …

[**Webinar on Unique Molecular Identifier-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study**][1] **Speaker**: Dr. Pandurang Kolekar, Bioinformatics Engineer, Strand Life Sciences **Abstract** Unique …

[Strand Life Sciences Announces the Release of Strand NGS v3.1 at ASHG 2017][1] Strand NGS now supports large scale RNA- and small-RNA-Seq and Unique Molecular …

**[Live Free Webinar on Leukocyte immunobiology helps us predict post-operative risk using pre-operative markers on 9 Aug, 8 am PST][1]** **Speaker**: Mario Deng MD FACC …

Continuing our [DNA-Seq webinar series][1], we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best practices workflow …

Dear all, please join and welcome the preprint of our latest study entitled "Pan-cancer scale landscape of simple somatic mutations" on bioRXiv [http://biorxiv.org/content/early/2017/02/28/112367][1]. Distinct mutational …

**Live Webinar on RNA-Seq Data Analysis** Abstract Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome …

[Implications of Next Generation Sequencing in Molecular Diagnosis of Cancer- Case studies][1] Abstract: Genetic testing requires screening of the entire gene, which by conventional sequencing …

[**Live webinar on 25 June: Copy Number Detection in Inherited Disorders and Somatic Cancer**][1] Register for free! http://www.strand-ngs.com/webinar_registration - Session 1: 25 June; 2:00 PM …