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

  • 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

Producción científica: Articlerevisión exhaustiva

98 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Número de artículo2546
PublicaciónNature Communications
Volumen14
N.º1
DOI
EstadoPublished - dic 2023

Nota bibliográfica

Publisher Copyright:
© 2023, The Author(s).

Financiación

We thank Jane Salant for her helpful comments on the manuscript. J.L., J.D., and N.L. acknowledge the support from the NSF ECCS-2038603. J.L. acknowledges the support from NIH/NIDDK 1DP1DK130673 and William F. Milton Fund. J.D. acknowledges the support from the Army Research Laboratory and the Army Research Office under grant number W911NF-20-1-0222. Y.H. acknowledges the support from the James Mills Peirce Fellowship from the Graduate School of Arts and Sciences of Harvard University. Schematics in Figs. a, a, and were partially created with BioRender.com.

FinanciadoresNúmero del financiador
William F. Milton Fund
DEVCOM Army Research Laboratory
National Institutes of Health (NIH)
Graduate School of Arts and Sciences, Harvard University
National Science Foundation Arctic Social Science ProgramECCS-2038603, 2038603
Army Research OfficeW911NF-20-1-0222
National Institute of Diabetes and Digestive and Kidney Diseases1DP1DK130673

    ASJC Scopus subject areas

    • General Chemistry
    • General Biochemistry, Genetics and Molecular Biology
    • General
    • General Physics and Astronomy

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