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ExomeModel 2.0 - Fixed Panels

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Twist Exome 2.0 is designed to detect rare and inherited diseases, as well as germline cancers. This panel’s high uniformity and low off-target rate deliver best-in-class sequencing efficiency, enabling quality data to be collected with less sequencing. With superior coverage of major genetic databases (RefSeq, CCDS, GenCode, Clinvar, ACMG73 and more) and the addition of clinically relevant non-coding pathogenic and likely pathogenic variants, Twist Exome 2.0 provides the value of multiple clinical panels all wrapped into one, easily customizable package.

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Coverage That Matters

  • Covers 36.5 Mb of human protein coding regions
  • Based on recent database releases
  • Includes carefully curated clinical content
  • Twist Exome 2.0 Benefit Coverage That Matters

Best-in-Class Performance

  • Uniform enrichment of target regions
  • NGS QC of all probes
  • Best-in-Class Performance Retain Flexibility

Retain Flexibility

  • Easily spike-in content into the exome
  • Effective across multiplex target enrichment workflows
  • Run overnight or same day workflows