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Predicting cell type-specific epigenomic profiles accounting for distal genetic effects

Author

Listed:
  • Alan E. Murphy

    (UK Dementia Research Institute at Imperial College London
    Imperial College London)

  • William Beardall

    (Imperial College London)

  • Marek Rei

    (Imperial College London)

  • Mike Phuycharoen

    (University of Manchester)

  • Nathan G. Skene

    (UK Dementia Research Institute at Imperial College London
    Imperial College London)

Abstract

Understanding how genetic variants affect the epigenome is key to interpreting GWAS, yet profiling these effects across the non-coding genome remains challenging due to experimental scalability. This necessitates accurate computational models. Existing machine learning approaches, while progressively improving, are confined to the cell types they were trained on, limiting their applicability. Here, we introduce Enformer Celltyping, a deep learning model which incorporates distal effects of DNA interactions, up to 100,000 base-pairs away, to predict epigenetic signals in previously unseen cell types. Using DNA and chromatin accessibility data for epigenetic imputation, Enformer Celltyping outperforms current best-in-class approaches and generalises across cell types and biological regions. Moreover, we propose a framework for evaluating models on genetic variant effect prediction using regulatory quantitative trait loci mapping studies, highlighting current limitations in genomic deep learning models. Despite this, Enformer Celltyping can also be used to study cell type-specific genetic enrichment of complex traits.

Suggested Citation

  • Alan E. Murphy & William Beardall & Marek Rei & Mike Phuycharoen & Nathan G. Skene, 2024. "Predicting cell type-specific epigenomic profiles accounting for distal genetic effects," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54441-5
    DOI: 10.1038/s41467-024-54441-5
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    References listed on IDEAS

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    1. David R Kelley, 2020. "Cross-species regulatory sequence activity prediction," PLOS Computational Biology, Public Library of Science, vol. 16(7), pages 1-27, July.
    2. Timothy J. Durham & Maxwell W. Libbrecht & J. Jeffry Howbert & Jeff Bilmes & William Stafford Noble, 2018. "PREDICTD PaRallel Epigenomics Data Imputation with Cloud-based Tensor Decomposition," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
    3. Yeda Wu & Graham K. Murray & Enda M. Byrne & Julia Sidorenko & Peter M. Visscher & Naomi R. Wray, 2021. "GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression," Nature Communications, Nature, vol. 12(1), pages 1-17, December.
    4. Anshul Kundaje & Wouter Meuleman & Jason Ernst & Misha Bilenky & Angela Yen & Alireza Heravi-Moussavi & Pouya Kheradpour & Zhizhuo Zhang & Jianrong Wang & Michael J. Ziller & Viren Amin & John W. Whit, 2015. "Integrative analysis of 111 reference human epigenomes," Nature, Nature, vol. 518(7539), pages 317-330, February.
    5. Carles A. Boix & Benjamin T. James & Yongjin P. Park & Wouter Meuleman & Manolis Kellis, 2021. "Regulatory genomic circuitry of human disease loci by integrative epigenomics," Nature, Nature, vol. 590(7845), pages 300-307, February.
    6. Vassily Trubetskoy & Antonio F. Pardiñas & Ting Qi & Georgia Panagiotaropoulou & Swapnil Awasthi & Tim B. Bigdeli & Julien Bryois & Chia-Yen Chen & Charlotte A. Dennison & Lynsey S. Hall & Max Lam & K, 2022. "Mapping genomic loci implicates genes and synaptic biology in schizophrenia," Nature, Nature, vol. 604(7906), pages 502-508, April.
    7. Jill E. Moore & Michael J. Purcaro & Henry E. Pratt & Charles B. Epstein & Noam Shoresh & Jessika Adrian & Trupti Kawli & Carrie A. Davis & Alexander Dobin & Rajinder Kaul & Jessica Halow & Eric L. No, 2020. "Expanded encyclopaedias of DNA elements in the human and mouse genomes," Nature, Nature, vol. 583(7818), pages 699-710, July.
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