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Old 04-17-2017, 03:10 AM   #1
Strandlife
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Default 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 practices workflow is twice as fast as its GATK counterpart, and results in precision/recall rates of up to 99%/98% on whole exome and whole genome samples. We'll also speak briefly about some of the other features in v3.0 including one-shot pipelines, TSS plots, RNA-Seq performance improvements, and, for the first time, HGVS notations for SNP effect analysis.

Speaker:
Dr. Radhakrishna Bettadapura, or RK, is a Senior Software Engineer at Strand Life Sciences. RK holds a Ph.D in Computational Biology and Mechanical Engineering from the University of Texas at Austin. Before his stint with the NGS team at Strand, he developed algorithms to model and analyse protein flexibility. At Strand, he works on precision and performance workflows for DNA-Seq and RNA-Seq.

Register here http://www.strand-ngs.com/webinar_registration

Last edited by Strandlife; 04-24-2017 at 05:16 AM.
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Old 04-24-2017, 05:37 AM   #2
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Hurry! Just 2 days left for the webinar on Fast and Accurate Variant Calling in Strand NGS v3.0. Register here http://www.strand-ngs.com/webinar_registration
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Old 05-16-2017, 01:51 AM   #3
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In case you missed the webinar, because of your busy schedule, do access the recording from here http://www.strand-ngs.com/learn/webinar-recordings
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