Results for "variant calling"


  • 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 Please visit our site at

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

    1244 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

    307 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

    107 days ago