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Uncover true biological signals in complex genomic samples

Maximize your detection sensitivity for low-frequency somatic variants in cell-free DNA (cfDNA) and genomic DNA (gDNA) samples. This system enables the generation of consensus reads to effectively filter out PCR-induced errors and artifacts. By providing unique molecular identifiers (UMI) and dual-indexed (UDI) primers, it supports high-accuracy variant calling for advanced research in oncology and other fields where precision is key.

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Enhance rare variant detection

Use matched molecular identifiers to build consensus reads that reveal true biological signals in low-abundance samples.

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Minimize sequencing artifacts

Distinguish true somatic mutations from PCR-induced errors and library preparation artifacts for higher confidence in variant calling.

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Ensure scalable workflows

Support both cfDNA and gDNA inputs with automation-friendly 16- or 96-sample formats in a 96-well plate configuration.

Product data

The Twist UMI Adapter System integrates seamlessly into existing library preparation workflows as a drop-in replacement for Twist Universal Adapters. The 5-bp-matched UMI adapters are first ligated to the input molecules and subsequently PCR-amplified with Twist’s Unique Dual-Indexed primers. The resulting indexed libraries enable post-sequencing consensus building, which offers higher detection sensitivity than standard methods. 

Twist's UMI Adapter System offers a tool for consensus building that removes errors from PCR duplicates.

Video
Illustration of the Twist UMI Adapter System workflow showing mechanical DNA fragmentation, end repair, A-tailing, UMI adapter ligation, and UDI primer PCR amplification to generate indexed sequencing libraries.
Scatter plot comparing sequencing error probability with and without UMI error correction across the capture space, demonstrating substantially lower error rates and improved sensitivity for variant detection with Twist UMI adapters.

Flexible workflow

The Twist UMI Adapter System integrates seamlessly into existing library preparation workflows as a drop-in replacement for Twist Universal Adapters. The 5-bp-matched UMI adapters are first ligated to the input molecules and subsequently PCR-amplified with Twist’s Unique Dual-Indexed primers. The resulting indexed libraries enable post-sequencing consensus building, which offers higher detection sensitivity than standard methods. 

Illustration of the Twist UMI Adapter System workflow showing mechanical DNA fragmentation, end repair, A-tailing, UMI adapter ligation, and UDI primer PCR amplification to generate indexed sequencing libraries.

Greater sensitivity in variant detection

Twist's UMI Adapter System offers a tool for consensus building that removes errors from PCR duplicates.

Scatter plot comparing sequencing error probability with and without UMI error correction across the capture space, demonstrating substantially lower error rates and improved sensitivity for variant detection with Twist UMI adapters.

Estimated per-base error rate for non-error-corrected reads (gray) and error-corrected reads (green) measured from target enrichment of a synthetic cfDNA standard. After sequencing, reads were downsampled to 20,000x coverage and error correction was performed using duplex collapse, requiring at least one read from each original strand.

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Illustration of the Twist UMI Adapter System workflow showing mechanical DNA fragmentation, end repair, A-tailing, UMI adapter ligation, and UDI primer PCR amplification to generate indexed sequencing libraries.

Flexible workflow

The Twist UMI Adapter System integrates seamlessly into existing library preparation workflows as a drop-in replacement for Twist Universal Adapters. The 5-bp-matched UMI adapters are first ligated to the input molecules and subsequently PCR-amplified with Twist’s Unique Dual-Indexed primers. The resulting indexed libraries enable post-sequencing consensus building, which offers higher detection sensitivity than standard methods. 

Scatter plot comparing sequencing error probability with and without UMI error correction across the capture space, demonstrating substantially lower error rates and improved sensitivity for variant detection with Twist UMI adapters.

Greater sensitivity in variant detection

Twist's UMI Adapter System offers a tool for consensus building that removes errors from PCR duplicates.

Which adapter system is right for you?

Twist's Adapter Systems improve the performance of any 'T-A' overhang ligation library preparation workflow for next-generation sequencing (NGS) applications. They reduce adapter dimer formation, increase yield, and can eliminate or minimize PCR—improving data quality while lowering sequencing costs. With broad compatibility, high multiplexing (up to 3,072 indexes), and ready-to-use formats, they scale effortlessly from discovery to high-throughput studies. Quality is in our DNA—All Twist adapters are functionally validated to ensure performance and reliability in all NGS applications.

Compare our adapter systems

UMI Adapter System

Full Length UDI Adapters

Universal Adapter System

HT Universal Adapter System

Adapter System - Trinity Freestyle

Best For

Improved NGS variant accuracy

PCR-free Whole Genome Sequencing

Most applications

High throughput applications

Used with the Trinity Fast Hyb Workflow

Contains

UMI Adapers; UDI Primers

Full Length UDI Adapters

Universal Adapters; UDI Primers

Universal Adapters; HT UDI Primers

Universal Adapters compatible with Trinity Freestyle Sequencing; UDI Primers

Unique indexes

16 or 384

1536

16 or 384

3072

384

Index length

10bp

12bp

10bp

12bp

10bp

Available formats

96-well plates

96-well plates

96-well plates

96- or 384-well plates

96-well plates

Sequencer Compatibility

Illumina

Element Cloudbreak Freestyle

Illumina

Element Cloudbreak Freestyle

Illumina

Element Cloudbreak Freestyle

Illumina

Element Cloudbreak Freestyle

Element Trinity Freestyle