Products & Reviews

Streamline the identification of heritable disease-linked alleles, be it through carrier screening or pre- and post-natal testing.

The Twist Alliance Clinical Research Exome helps support the Broad Institute Genomics Platform and was designed using validated data from clinical patient samples.

The Twist Alliance Canine Exome developed in collaboration with the Broad Institute

The Twist Alliance CNTG Exome - 41 MB provides highly uniform coverage of the entire exome as well as full coverage of the mitochondrial genome.

Coverage of rare disease-associated genes 

Coverage of 72 selected cancer-associated genes

Detect Multiple Viral Pathogens from a Single Sample

Fast and Easy Library Workflows

Sequence the Whole Transcriptome

Outstanding Performance with Targetd Exome Sequencing

The Twist NGS Methylation Detection System provides a robust, end-to-end sample preparation solution for identifying methylated regions in the human genome. The workflow employs a unique enzymatic process from New England Biolabs® that is much less damaging to DNA, alongside Twist‘s Custom Methylation Panel design.

The Twist Bioscience MRD Rapid 500 Panel is a scalable target enrichment solution for monitoring minimal residual disease that leverages Twist’s silicon based DNA synthesis platform to design and manufacture capture panels for personalized medicine. 

The Twist UMI Adapter system offers a sensitive method for identifying low frequency somatic variants from cell free DNA (cfDNA). Libraries prepared with the UMI adapter system can be used for building consensus reads during analysis to increase variant detection sensitivity and to reduce PCR error contribution.

The Twist Pan-cancer Reference Standard is a high-quality, standardized control for use in the research and development of NGS-based liquid biopsy assays. 

Twist’s RNA sequencing workflows offer a complete NGS solution that produces uniform libraries for RNA sequencing.