Abstract 7205: A universal duplex sequencing approach for accurate detection of somatic mutations

Abstract Somatic mutations arise from endogenous and exogenous mutagenic processes, accumulating over time and contributing to aging and disease. Detecting these rare mutations in non-clonal tissues remains a significant challenge due to the high error rates, limited genome coverage, and substantial DNA input requirements of existing sequencing approaches. Here, we introduce UDSeq, a high-accuracy, cost-effective, single-molecule duplex sequencing protocol designed to overcome these limitations. We place UDSeq in the context of existing duplex sequencing approaches, demonstrating that it achieves an exceptionally low error rate of ∼2.5 × 10-9 per base pair, supports whole-genome and targeted capture sequencing from as little as 100 picograms of DNA, and delivers up to four times more usable duplex molecules than current state-of-the-art methods from the same input. We demonstrated the broad applicability of UDSeq through a series of in vitro and in vivo mutagenesis experiments, accurately capturing known mutational signatures induced by environmental carcinogens in human cell lines, rodents, and non-model organisms. We further applied UDSeq to normal tissues from a 70-year-old individual, revealing organ-specific mutational burdens and the activity of distinct mutational processes. With its high accuracy, low input requirements, and wide applicability, UDSeq provides a powerful and scalable tool for studying mutational processes across diverse biological contexts. Its versatility supports applications in cancer research, aging, and environmental exposure, expanding our capacity to characterize somatic mutations in both healthy and diseased tissues. Citation Format: Shuvro Prokash Nandi, Yuhe Cheng, Shams Al-azzam, Safa Saeed, Isabella R Stuewe, Zichen Jiang, Luka Culibrk, Maria Zhivagui, Xiaoxu Yang, Rachel M. Wise, Foster C. Jacobs, Bérénice Chavanel, Michael Korenjak, Mia PETLJAK, Silvia Balbo, Laurie G. Hudson, Ke Jian Liu, Jiri Zavadil, Joseph G. Gleeson, Ludmil B. Alexandrov. A universal duplex sequencing approach for accurate detection of somatic mutations [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7205.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7205
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 7205: A universal duplex sequencing approach for accurate detection of somatic mutations

Ke Jian Liu, Mia Petljak, Rachel M. Wise, Michael Korenjak et al.
Cancer Research
Cancer Genomics and Diagnostics
article

Abstract 7205: A universal duplex sequencing approach for accurate detection of somatic mutations

Ke Jian Liu, Mia Petljak, Rachel M. Wise, Michael Korenjak, Shams Al-Azzam, Maria Zhivagui, Laurie G. Hudson, Foster C. Jacobs, Shuvro P. Nandi, Silvia Balbo, Ludmil B. Alexandrov, Luka Culibrk, Xiaoxu Yang, Bérénice Chavanel, Yuhe Cheng, Jiří Zavadil, Isabella Stuewe, Safa Saeed, Zichen Jiang, Joseph G. Gleeson
article en

Abstract

Abstract Somatic mutations arise from endogenous and exogenous mutagenic processes, accumulating over time and contributing to aging and disease. Detecting these rare mutations in non-clonal tissues remains a significant challenge due to the high error rates, limited genome coverage, and substantial DNA input requirements of existing sequencing approaches. Here, we introduce UDSeq, a high-accuracy, cost-effective, single-molecule duplex sequencing protocol designed to overcome these limitations. We place UDSeq in the context of existing duplex sequencing approaches, demonstrating that it achieves an exceptionally low error rate of ∼2.5 × 10-9 per base pair, supports whole-genome and targeted capture sequencing from as little as 100 picograms of DNA, and delivers up to four times more usable duplex molecules than current state-of-the-art methods from the same input. We demonstrated the broad applicability of UDSeq through a series of in vitro and in vivo mutagenesis experiments, accurately capturing known mutational signatures induced by environmental carcinogens in human cell lines, rodents, and non-model organisms. We further applied UDSeq to normal tissues from a 70-year-old individual, revealing organ-specific mutational burdens and the activity of distinct mutational processes. With its high accuracy, low input requirements, and wide applicability, UDSeq provides a powerful and scalable tool for studying mutational processes across diverse biological contexts. Its versatility supports applications in cancer research, aging, and environmental exposure, expanding our capacity to characterize somatic mutations in both healthy and diseased tissues. Citation Format: Shuvro Prokash Nandi, Yuhe Cheng, Shams Al-azzam, Safa Saeed, Isabella R Stuewe, Zichen Jiang, Luka Culibrk, Maria Zhivagui, Xiaoxu Yang, Rachel M. Wise, Foster C. Jacobs, Bérénice Chavanel, Michael Korenjak, Mia PETLJAK, Silvia Balbo, Laurie G. Hudson, Ke Jian Liu, Jiri Zavadil, Joseph G. Gleeson, Ludmil B. Alexandrov. A universal duplex sequencing approach for accurate detection of somatic mutations [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7205.

Cancer ResearchVol. 86(7_Supplement)
New Mexico Department of Health (US), University of Minnesota (US), Children’s Institute (US), University of Nevada, Las Vegas (US), University of New Mexico (US), University of Utah (US), UC San Diego Health System (US), NYU Langone Health (US), Stony Brook School (US), Stony Brook Medicine (US), La Jolla Alcohol Research (US), University of Minnesota Medical Center (US), Centre international de recherche sur le cancer (FR), Moores Cancer Center, New York University (US)
Openalex Percentile: Top 11%
Cancer Genomics and Diagnostics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.