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Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA

Author

Listed:
  • Mingyun Bae

    (Department of Bio and Brain Engineering, KAIST)

  • Gyuhee Kim

    (Department of Bio and Brain Engineering, KAIST)

  • Tae-Rim Lee

    (Genome Research Center, GC Genome)

  • Jin Mo Ahn

    (Genome Research Center, GC Genome)

  • Hyunwook Park

    (Department of Bio and Brain Engineering, KAIST)

  • Sook Ryun Park

    (University of Ulsan College of Medicine)

  • Ki Byung Song

    (Asan Medical Center, University of Ulsan College of Medicine)

  • Eunsung Jun

    (Asan Medical Center, University of Ulsan College of Medicine)

  • Dongryul Oh

    (Sungkyunkwan University School of Medicine)

  • Jeong-Won Lee

    (Sungkyunkwan University School of Medicine)

  • Young Sik Park

    (Seoul National University Hospital)

  • Ki-Won Song

    (University of Ulsan College of Medicine)

  • Jeong-Sik Byeon

    (University of Ulsan College of Medicine)

  • Bo Hyun Kim

    (National Cancer Center)

  • Joo Hyuk Sohn

    (Yonsei University College of Medicine
    AIMA, Inc., Avison Biomedical Research Center)

  • Min Hwan Kim

    (Yonsei University College of Medicine)

  • Gun Min Kim

    (Yonsei University College of Medicine)

  • Eui Kyu Chie

    (Seoul National University College of Medicine)

  • Hyun-Cheol Kang

    (Seoul National University College of Medicine)

  • Sun-Young Kong

    (National Cancer Center)

  • Sang Myung Woo

    (National Cancer Center)

  • Jeong Eon Lee

    (Samsung Medical Center)

  • Jai Min Ryu

    (Samsung Medical Center)

  • Junnam Lee

    (Genome Research Center, GC Genome)

  • Dasom Kim

    (Genome Research Center, GC Genome)

  • Chang-Seok Ki

    (Genome Research Center, GC Genome)

  • Eun-Hae Cho

    (Genome Research Center, GC Genome)

  • Jung Kyoon Choi

    (Department of Bio and Brain Engineering, KAIST)

Abstract

Multi-cancer early detection remains a key challenge in cell-free DNA (cfDNA)-based liquid biopsy. Here, we perform cfDNA whole-genome sequencing to generate two test datasets covering 2125 patient samples of 9 cancer types and 1241 normal control samples, and also a reference dataset for background variant filtering based on 20,529 low-depth healthy samples. An external cfDNA dataset consisting of 208 cancer and 214 normal control samples is used for additional evaluation. Accuracy for cancer detection and tissue-of-origin localization is achieved using our algorithm, which incorporates cancer type-specific profiles of mutation distribution and chromatin organization in tumor tissues as model references. Our integrative model detects early-stage cancers, including those of pancreatic origin, with high sensitivity that is comparable to that of late-stage detection. Model interpretation reveals the contribution of cancer type-specific genomic and epigenomic features. Our methodologies may lay the groundwork for accurate cfDNA-based cancer diagnosis, especially at early stages.

Suggested Citation

  • Mingyun Bae & Gyuhee Kim & Tae-Rim Lee & Jin Mo Ahn & Hyunwook Park & Sook Ryun Park & Ki Byung Song & Eunsung Jun & Dongryul Oh & Jeong-Won Lee & Young Sik Park & Ki-Won Song & Jeong-Sik Byeon & Bo H, 2023. "Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37768-3
    DOI: 10.1038/s41467-023-37768-3
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