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Reliable, scalable cfDNA workflows

Generate high-quality libraries from challenging cfDNA inputs with a streamlined workflow that delivers high conversion and sensitivity for rare variant detection. Designed for low input and fragmented samples, the Twist cfDNA Library Prep Kit helps you uncover critical insights with confidence and efficiency.

Fiable

Maximice la detección de variantes infrecuentes

La alta tasa de conversión detecta con fiabilidad las variantes infrecuentes (≤0,1 % VAF) Support duplex sequencing workflows with the Twist UMI Adapter System to maximize detection sensitivity.

muestras

Streamlined workflow for precious samples

Achieve robust performance, even with low (<1 ng) sample input. Get sequence-ready libraries in 2 hours.

detección

Amplificación sin sesgo

Get consistent coverage across 5%–95% GC, preserving challenging genomic regions and difficult-to-capture targets. Get consistent high yields from complex libraries, even at ≤100 pg of DNA input. Call variants with confidence.

Datos del producto

High-fidelity amplification with Twist TrueAmp Polymerase generates cfDNA libraries that have substitution error rates comparable to those of PCR-free cfDNA libraries across all analyzed base changes.

The Twist cfDNA Library Prep Kit delivers higher cfDNA library yields. Following library generation, samples were eluted in 20 μL of water, and 1 µL was quantified with Qubit™ dsDNA Broad Range Kit.

The Twist cfDNA Library Prep Kit enables sensitive, accurate detection down to 0.25% VAF. Single-plex capture with a 50 kb oncology panel targets 217 single nucleotide polymorphisms (SNPs). Las variantes omitidas son sitios con <1 familia de variantes sobre el total de sitios detectables.

The Twist cfDNA Library Prep Kit delivers higher library complexity with or without unique molecular identifier (UMI) deduplication. Single-plex capture with a 50 kb oncology panel targets variant sites in cfDNA standard material using optimized target enrichment workflows.

Vídeo
cfDNA sequencing error rate comparison showing PCR-free vs TrueAmp amplification libraries with equivalent base substitution accuracy for low-frequency variant detection
cfDNA library preparation kit generating higher DNA yield measured by Qubit™, improving NGS library prep efficiency and sequencing performance
Sensitive detection of low-frequency variants at 0.25% VAF using cfDNA library prep and hybridization capture with oncology SNP panel
High-complexity cfDNA sequencing libraries with and without UMI deduplication, improving unique read depth and variant detection accuracy

High-fidelity amplification with PCR

High-fidelity amplification with Twist TrueAmp Polymerase generates cfDNA libraries that have substitution error rates comparable to those of PCR-free cfDNA libraries across all analyzed base changes.

cfDNA sequencing error rate comparison showing PCR-free vs TrueAmp amplification libraries with equivalent base substitution accuracy for low-frequency variant detection

Figure 1 Comparable Base Substitution Error Rates with and without TrueAmp Amplification. The Twist cfDNA Library Prep Kit was used to generate libraries with the Twist cfDNA Pan-Cancer Reference Standard v2 as the input material. Twist Full-Length Unique Dual Index (UDI) Adapters were used during ligation for the PCR-free condition and Twist Universal Adapters were used during ligation for the PCR condition. La condición de PCR se amplificó utilizando 6 ciclos con mezcla de polimerasa TrueAmp Twist y cebadores de UDI. Las bibliotecas se agruparon, secuenciaron y analizaron. Se observan tasas de error comparables entre las bibliotecas sin PCR y TrueAmp.

Tasa de conversión más alta = rendimiento más alto

The Twist cfDNA Library Prep Kit delivers higher cfDNA library yields. Following library generation, samples were eluted in 20 μL of water, and 1 µL was quantified with Qubit™ dsDNA Broad Range Kit.

cfDNA library preparation kit generating higher DNA yield measured by Qubit™, improving NGS library prep efficiency and sequencing performance

Figura 2. The Twist cfDNA Library Prep Kit delivers higher cfDNA library yields. Following library generation, samples were eluted in 20 uL of water, and 1 uL was quantified with Qubit™ dsDNA Broad Range Kit.

Mayor sensibilidad y mayor precisión

The Twist cfDNA Library Prep Kit enables sensitive, accurate detection down to 0.25% VAF. Single-plex capture with a 50 kb oncology panel targets 217 single nucleotide polymorphisms (SNPs). Las variantes omitidas son sitios con <1 familia de variantes sobre el total de sitios detectables.

Sensitive detection of low-frequency variants at 0.25% VAF using cfDNA library prep and hybridization capture with oncology SNP panel

Figura 3. The Twist cfDNA Library Prep Kit enables sensitive and accurate detection of variants at 0.25% VAF. Las bibliotecas se capturaron monoplexadas con un panel oncológico personalizado de 50 kb dirigido a los sitios de variantes de 217 SNP en el material estándar pantumoral. Las variantes ausentes se calculan sumando los sitios con menos de 1 familia de variantes y dividiendo el resultado entre el número de sitios de variantes detectables totales.

Duplexión mejorada = mayor complejidad

The Twist cfDNA Library Prep Kit delivers higher library complexity with or without unique molecular identifier (UMI) deduplication. Single-plex capture with a 50 kb oncology panel targets variant sites in cfDNA standard material using optimized target enrichment workflows.

High-complexity cfDNA sequencing libraries with and without UMI deduplication, improving unique read depth and variant detection accuracy

Figura 4. The Twist cfDNA Library Prep Kit delivers higher complexity with and without UMI deduplication.

1/5
cfDNA sequencing error rate comparison showing PCR-free vs TrueAmp amplification libraries with equivalent base substitution accuracy for low-frequency variant detection

High-fidelity amplification with PCR

High-fidelity amplification with Twist TrueAmp Polymerase generates cfDNA libraries that have substitution error rates comparable to those of PCR-free cfDNA libraries across all analyzed base changes.

cfDNA library preparation kit generating higher DNA yield measured by Qubit™, improving NGS library prep efficiency and sequencing performance

Tasa de conversión más alta = rendimiento más alto

The Twist cfDNA Library Prep Kit delivers higher cfDNA library yields. Following library generation, samples were eluted in 20 μL of water, and 1 µL was quantified with Qubit™ dsDNA Broad Range Kit.

Sensitive detection of low-frequency variants at 0.25% VAF using cfDNA library prep and hybridization capture with oncology SNP panel

Mayor sensibilidad y mayor precisión

The Twist cfDNA Library Prep Kit enables sensitive, accurate detection down to 0.25% VAF. Single-plex capture with a 50 kb oncology panel targets 217 single nucleotide polymorphisms (SNPs). Las variantes omitidas son sitios con <1 familia de variantes sobre el total de sitios detectables.

High-complexity cfDNA sequencing libraries with and without UMI deduplication, improving unique read depth and variant detection accuracy

Duplexión mejorada = mayor complejidad

The Twist cfDNA Library Prep Kit delivers higher library complexity with or without unique molecular identifier (UMI) deduplication. Single-plex capture with a 50 kb oncology panel targets variant sites in cfDNA standard material using optimized target enrichment workflows.

The cfDNA Library Prep Kit with TrueAmp Polymerase Mix workflow
The cfDNA workflow leverages engineered GC balance and high-fidelity amplification. This design delivers high amplification yield while minimizing PCR-introduced errors that can compromise low-frequency variant detection. El resultado son bibliotecas uniformes y de alta calidad en un flujo de trabajo rápido de 2 horas. El control de arranque en caliente basado en aptámeros proporciona estabilidad a temperatura ambiente para la configuración automatizada, mientras que la mezcla maestra de tubo único 2× agiliza los flujos de trabajo de WGS y de enriquecimiento del objetivo.
cfDNA NGS workflow with optimized GC balance and high-fidelity PCR amplification delivering uniform libraries, reduced sequencing errors, and improved low-frequency variant detection
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