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Webinar-Diagnosis of Rare Diseases using NGS Based Multi-gene Testing-Case studies
A disease is considered to be ‘rare’ when it affects one in about 2000 individuals in the population. This, individually are although rare,...Last edited by Strandlife; 03-19-2018, 01:29 AM. -
Live Webinar on RNA-Seq Data Analysis on 28 Feb 2018
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... -
Webinar-Unravelling complex mutational events in clinical cases using NGS analysis
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Live Webinar on UMI-powered Ultra-sensitive Variant Calling on 13 Dec 2017
Live Webinar on Unique Molecular Identifier-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study by Dr.Pandurang Kolekar, on 13 Dec... -
Unique Molecular Identifiers Workflow Support -Now in Strand NGS v3.1
Unique Molecular Identifiers, or UMIs, are short sequences (6-12bp) added to sequencing libraries prior to PCR amplification. UMIs can improve the accuracy... -
Decoding Breast Cancer using DNA Variant analysis
Decoding Breast Cancer using Strand NGS DNA Variant analysis
Molecular diagnosis of hereditary breast cancer is majorly based on the identification... -
Strand Life Sciences to showcase Strand NGS at ASHG 2017, Florida
Strand Life Sciences to showcase Strand NGS, analysis software for next-generation sequencing data at ASHG 2017
Scientists from Strand... -
Strandlife started a topic Webinar on NGS Gene Expression Analysis in GeneSpring GX 14.9 on 6th Sep, 8AM PSTin GeneralWebinar on NGS Gene Expression Analysis in GeneSpring GX 14.9 on 6th Sep, 8AM PST
Live webinar on NGS Gene Expression Analysis in GeneSpring GX 14.9
Speaker: Bandana Gupta, Application Scientist, Agilent Technologies... -
Webinar on Leukocyte immunobiology by Dr. Mario Deng on 9 Aug 2017
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Live Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Continuing our webinar series, we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best...Last edited by Strandlife; 04-24-2017, 05:16 AM. -
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Presenting Strand NGS v3.0 best-practices: a DNA-Seq workflow that identifies highly accurate variants from raw reads. Our best practices workflow is... -
Live Webinar on RNA-Seq Data Analysis on 9 Nov 2016
Live Webinar on RNA-Seq Data Analysis
Abstract:
Strand NGS supports an extensive workflow for the analysis and visualization of... -
Reduce the SNP annotation time by up to 95%
Explore the new script ‘Create Targeted VAL’ in Strand NGS for creating subset of dbSNP database with target regions of interest and run...Last edited by Strandlife; 07-03-2016, 10:29 PM. -
Live webinar on 26 Aug: Calling narrow and broad peaks from ChIP-Seq data
Live webinar: Calling narrow and broad peaks from ChIP-Seq data on 26 Aug 2015
Abstract
Chromatin immunoprecipitation (ChIP) followed... -
Calling narrow and broad peaks from ChIP-Seq data - Benchmarking study
Know about the state-of-the-art algorithms implemented in Strand NGS for detecting the binding sites of transcription factor (narrow peaks) and enriched...