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Old 04-17-2017, 03:05 AM   #1
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Default 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 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. This live webinar will also cover 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
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dna-seq, ngs data analysis, strand ngs, variant calling, webinar

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