Skip to main content
メニュー
Revvity logo
Contact us
JP
Revvity Sites Globally

Select your location.

*e-commerce not available for this region.

australia.webp Australia
austria.webp Austria
belgium.webp Belgium
brazil.webp Brazil *
canada.webp Canada
china.webp China *
denmark.webp Denmark
finland.webp Finland
france.webp France
germany.webp Germany
hong-kong.webp Hong Kong (China) *
india.webp India *
ireland.webp Ireland
italy.webp Italy
japan.webp Japan *
luxembourg.webp Luxembourg
mexico.webp Mexico *
netherlands.webp Netherlands
norway.webp Norway
philippines.webp Philippines *
republic of korea.webp Republic of Korea *
singapore.webp Singapore *
spain.webp Spain
sweden.webp Sweden
switzerland.webp Switzerland
thailand.webp Thailand *
uk.webp United Kingdom
usa.webp United States
Breadcrumb
...
  • ホーム
  • Improved variant calling with the automated IDT xGen cfDNA & FFPE DNA Library Prep v2 MC Kit
idt xgen cfdna and ffpe library prep kit
Application Note

Improved variant calling with the automated IDT xGen cfDNA & FFPE DNA Library Prep v2 MC Kit

Working with circulating cell-free DNA (cfDNA) and formalin-fixed paraffin-embedded (FFPE) samples presents a unique set of challenges for molecular biologists, particularly when preparing them for next-generation sequencing (NGS).

The automated workflow of the IDT™ xGen™ cfDNA & FFPE DNA Library Prep v2 MC Kit is vendor-qualified and shows its value when generating libraries for sequencing or preparing samples for hybridization capture. The quality of the automated NGS libraries was measured using key metrics and compared to DNA libraries generated manually. 

Beyond simply preparing the library, the kit allows for generating higher-quality data on the first run, reducing the need for re-sequencing with:

  • Unique Molecular Identifiers (UMIs),
  • Better representation of the original sample.

Primary applications: 

  • Liquid biopsy studies using cfDNA
  • Oncology research using FFPE samples
  • Minimal residual disease (MRD) research to detect ultra-low-frequency variants
  • Whole genome sequencing (WGS) from degraded samples
  • Targeted sequencing using hybridization capture
  • Identification of germline and somatic variants like single nucleotide polymorphisms (SNPs) and insertions/deletions (indels).

To further increase your lab's efficiency, this method is fully automated and vendor-qualified on the Sciclone™ G3 NGSx liquid handler.


For research use only. Not for use in diagnostic procedures.

To view the full content please answer a few questions

By submitting my personal data, I acknowledge that Revvity Inc. and its affiliates (“Company”) will process my personal data provided above consistent with the Company’s Privacy Policy available here.

CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

Download Resource

Improved variant calling with the automated IDT xGen cfDNA & FFPE DNA Library Prep v2 MC Kit

Download Application Note
Revvity Logo

©2025 Revvity - All rights reserved

Revvity is a trademark of Revvity, Inc. All other trademarks are the property of their respective owners.