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Explainable multi-task learning for multi-modality biological data analysis

Author

Listed:
  • Xin Tang

    (Harvard University
    Broad Institute of MIT and Harvard)

  • Jiawei Zhang

    (University of Minnesota Twin Cities)

  • Yichun He

    (Harvard University
    Broad Institute of MIT and Harvard)

  • Xinhe Zhang

    (Harvard University)

  • Zuwan Lin

    (Harvard University)

  • Sebastian Partarrieu

    (Harvard University)

  • Emma Bou Hanna

    (Harvard University)

  • Zhaolin Ren

    (Harvard University)

  • Hao Shen

    (Harvard University)

  • Yuhong Yang

    (University of Minnesota Twin Cities)

  • Xiao Wang

    (Broad Institute of MIT and Harvard
    MIT)

  • Na Li

    (Harvard University)

  • Jie Ding

    (University of Minnesota Twin Cities)

  • Jia Liu

    (Harvard University)

Abstract

Current biotechnologies can simultaneously measure multiple high-dimensional modalities (e.g., RNA, DNA accessibility, and protein) from the same cells. A combination of different analytical tasks (e.g., multi-modal integration and cross-modal analysis) is required to comprehensively understand such data, inferring how gene regulation drives biological diversity and functions. However, current analytical methods are designed to perform a single task, only providing a partial picture of the multi-modal data. Here, we present UnitedNet, an explainable multi-task deep neural network capable of integrating different tasks to analyze single-cell multi-modality data. Applied to various multi-modality datasets (e.g., Patch-seq, multiome ATAC + gene expression, and spatial transcriptomics), UnitedNet demonstrates similar or better accuracy in multi-modal integration and cross-modal prediction compared with state-of-the-art methods. Moreover, by dissecting the trained UnitedNet with the explainable machine learning algorithm, we can directly quantify the relationship between gene expression and other modalities with cell-type specificity. UnitedNet is a comprehensive end-to-end framework that could be broadly applicable to single-cell multi-modality biology. This framework has the potential to facilitate the discovery of cell-type-specific regulation kinetics across transcriptomics and other modalities.

Suggested Citation

  • Xin Tang & Jiawei Zhang & Yichun He & Xinhe Zhang & Zuwan Lin & Sebastian Partarrieu & Emma Bou Hanna & Zhaolin Ren & Hao Shen & Yuhong Yang & Xiao Wang & Na Li & Jie Ding & Jia Liu, 2023. "Explainable multi-task learning for multi-modality biological data analysis," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37477-x
    DOI: 10.1038/s41467-023-37477-x
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    References listed on IDEAS

    as
    1. Gökcen Eraslan & Lukas M. Simon & Maria Mircea & Nikola S. Mueller & Fabian J. Theis, 2019. "Single-cell RNA-seq denoising using a deep count autoencoder," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
    2. Yichun He & Xin Tang & Jiahao Huang & Jingyi Ren & Haowen Zhou & Kevin Chen & Albert Liu & Hailing Shi & Zuwan Lin & Qiang Li & Abhishek Aditham & Johain Ounadjela & Emanuelle I. Grody & Jian Shu & Ji, 2021. "ClusterMap for multi-scale clustering analysis of spatial gene expression," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    3. Karren Dai Yang & Anastasiya Belyaeva & Saradha Venkatachalapathy & Karthik Damodaran & Abigail Katcoff & Adityanarayanan Radhakrishnan & G. V. Shivashankar & Caroline Uhler, 2021. "Multi-domain translation between single-cell imaging and sequencing data using autoencoders," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    4. Robrecht Cannoodt & Wouter Saelens & Louise Deconinck & Yvan Saeys, 2021. "Spearheading future omics analyses using dyngen, a multi-modal simulator of single cells," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
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