Twist Exome 2.0
Twist Exome 2.0 is a comprehensive exome sequencing panel designed to detect rare and inherited diseases, as well as germline cancers. Its high uniformity and low off-target rate deliver best-in-class sequencing efficiency, enabling quality data collection with less sequencing.
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Twist Exome 2.0 is engineered to provide deep coverage of all genes linked to clinical phenotypes, facilitating translational research across a wide range of conditions. Covering 36.5 Mb of human protein-coding regions, this panel is based on recent database releases and includes carefully curated clinical content. Its high uniformity and low off-target rate result in best-in-class sequencing efficiency, allowing for quality data collection with less sequencing. The panel's superior coverage of major genetic databases, such as RefSeq, CCDS, GenCode, ClinVar, and ACMG73, along with the inclusion of clinically relevant non-coding pathogenic and likely pathogenic variants, provides the value of multiple clinical panels in one customizable package.
Key features:
- Comprehensive Coverage: Covers 36.5 Mb of human protein-coding regions, including carefully curated clinical content.
- Best-in-Class Performance: Delivers high uniformity and low off-target rates, ensuring efficient and accurate sequencing.
- Customizable Flexibility: Easily allows for the addition of custom content to target regions of interest, accommodating specific research needs.
Applications:
- Rare and Inherited Disease Research: Enables the detection of genetic variants associated with rare diseases and inherited disorders.
- Germline Cancer Studies: Facilitates the identification of germline mutations linked to cancer susceptibility.
- Translational Research: Supports studies aiming to translate genetic findings into clinical applications.
For research use only. Not for use in diagnostic procedures.
