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Thread | Thread Starter | Forum | Replies | Last Post |
Live webinar on DNA-Seq Data Analysis - Selected Case Studies on 22 Feb 2017 | Strandlife | Webinar Series | 3 | 07-26-2017 05:10 AM |
Live Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 | Strandlife | General | 2 | 05-16-2017 02:51 AM |
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 | Strandlife | Bioinformatics | 0 | 04-17-2017 04:05 AM |
Live webinar Tue Aug 25: MetaSV - An accurate & integrative structura variant caller | jenny.hsu | Events / Conferences | 0 | 08-14-2015 02:59 PM |
Live webinar on 26 Aug: Calling narrow and broad peaks from ChIP-Seq data | Strandlife | Events / Conferences | 0 | 08-06-2015 03:52 AM |
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#1 |
strandlife
Location: All over the world Join Date: May 2013
Posts: 67
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Live Webinar on Unique Molecular Identifier-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study by Dr.Pandurang Kolekar, on 13 Dec at 2:30 PM IST and 9:30 PM IST
Abstract: 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. UMI-tagged NGS libraries allow, ultra-sensitive detection of low frequency variants from liquid biopsy samples using DNA-Seq and accurate quantification of transcript-level expression using RNA-Seq. The recent release of Strand NGS v3.1, is equipped with the necessary features to efficiently analyse UMI-tagged NGS data helping researchers and labs involved in rare variant calling like in cfDNA based cancer diagnostics, and accurate transcript quantification with RNA-Seq. To attend register here: http://www.strand-ngs.com/webinar_registration |
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#2 |
strandlife
Location: All over the world Join Date: May 2013
Posts: 67
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Read through this article on 'UMI-Powered Ultra-Sensitive Variant Calling with Strand NGS' to know more about the unique molecular identifiers, challenges and oppurtunities
https://www.linkedin.com/pulse/umi-p...d-ngs-kolekar/ Do register for the upcoming webinar by Dr.Pandurang Kolekar scheduled on 13 Dec at 2:30 PM IST and 9:30 PM IST. Register for webinar at http://www.strand-ngs.com/webinar_registration |
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#3 |
strandlife
Location: All over the world Join Date: May 2013
Posts: 67
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Hurry! Limited seats available. To attend, register at
http://www.strand-ngs.com/webinar_registration |
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Tags |
bioos, qiagen, strand ngs, umi, variant calling |
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