Results for "variant calling"

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  • NGS Online Training

    ArrayGen Technologies announces to provide online NGS training through out the globe. Now analyze your own NGS datasets from anywhere.For more information contact us at training@arraygen.com Please visit our site at www.arraygen.com

    Tags: Bioinformatics, NGS Data Analysis, Genomics, Exome sequencing, variant calling

    1154 days ago

  • Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017

    Continuing our DNA-Seq 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...

    Tags: webinar, strand ngs, variant calling, dna-seq, bwa-gatk

    217 days ago

  • Webinar on Unique Molecular Identifier (UMI)-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study

    Webinar on Unique Molecular Identifier-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study by Dr. Pandurang Kolekar, Bioinformatics Engineer, Strand Life Sciences Abstract: Unique Molecular Identifiers (UMIs) are short random nucleotide sequences that are increasingly be...

    Tags: UMI, Strand NGS, Variant calling, RNA-Seq, small RNA-Seq

    17 days ago