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	Live Webinar on Unique Molecular Identifier (UMI) - powered Ultra-sensitive Variant Calling using Strand NGS - Case Study Unique Molecular Identifiers (UMIs) are short random nucleotide sequences that are increasingly being used in high-throughput sequencing experiments. In this webinar, we will highlight the UMI-friendly features of Strand NGS v3.1 including support for handling well known and customised UMI libraries, QC metrics, consensus alignment, UMI-based family size filters for read list, genome browser enabled with UMI-specific features and filters, UMI-aware variant calling parameters, and exporting UMI-tagged aligned samples. These all features together empower users to harness the potential of UMI-tagged NGS data for deeper insights. A case study demonstrating application of these UMI-based features in Strand NGS for low frequency variant calling in cfDNA sample will be presented. Dr. Pandurang Kolekar Bioinformatics Engineer Strand Life Sciences
Session 1: 13 Dec 2017, 2:30 PM IST Session 2: 13 Dec 2017, 9:30 PM IST Register here
	Short Videos Strand NGS - Server Edition   One-shot Pipeline for DNA-Seq   Elastic Genome Browser Past Webinars Transcriptome Analysis to Investigate Hox Gene Functions By Srikanthi Ramachandrula, Senior Application Scientist, Strand Life Sciences   Integration of NGS & Machine Learning for prediction of post-operative recovery By Dr Mario Deng MD FACC FESC, David Geffen School of Medicine at UCLA   ChIP-Seq Analysis of Fibroblasts Under Oxidative Stress By Srikanthi Ramachandrula, Senior Application Scientist, Strand Life Sciences   2017 © Strand Life Sciences. All rights reserved. To receive updates from Strand, please subscribe here and forward to a friend. If you do not wish to receive emails from Strand, you can unsubscribe here