IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1007677.html
   My bibliography  Save this article

Multiview learning for understanding functional multiomics

Author

Listed:
  • Nam D Nguyen
  • Daifeng Wang

Abstract

The molecular mechanisms and functions in complex biological systems currently remain elusive. Recent high-throughput techniques, such as next-generation sequencing, have generated a wide variety of multiomics datasets that enable the identification of biological functions and mechanisms via multiple facets. However, integrating these large-scale multiomics data and discovering functional insights are, nevertheless, challenging tasks. To address these challenges, machine learning has been broadly applied to analyze multiomics. This review introduces multiview learning—an emerging machine learning field—and envisions its potentially powerful applications to multiomics. In particular, multiview learning is more effective than previous integrative methods for learning data’s heterogeneity and revealing cross-talk patterns. Although it has been applied to various contexts, such as computer vision and speech recognition, multiview learning has not yet been widely applied to biological data—specifically, multiomics data. Therefore, this paper firstly reviews recent multiview learning methods and unifies them in a framework called multiview empirical risk minimization (MV-ERM). We further discuss the potential applications of each method to multiomics, including genomics, transcriptomics, and epigenomics, in an aim to discover the functional and mechanistic interpretations across omics. Secondly, we explore possible applications to different biological systems, including human diseases (e.g., brain disorders and cancers), plants, and single-cell analysis, and discuss both the benefits and caveats of using multiview learning to discover the molecular mechanisms and functions of these systems.

Suggested Citation

  • Nam D Nguyen & Daifeng Wang, 2020. "Multiview learning for understanding functional multiomics," PLOS Computational Biology, Public Library of Science, vol. 16(4), pages 1-26, April.
  • Handle: RePEc:plo:pcbi00:1007677
    DOI: 10.1371/journal.pcbi.1007677
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1007677
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1007677&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1007677?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Witten Daniela M & Tibshirani Robert J., 2009. "Extensions of Sparse Canonical Correlation Analysis with Applications to Genomic Data," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 8(1), pages 1-29, June.
    2. Hossein Zare & Mostafa Kaveh & Arkady Khodursky, 2011. "Inferring a Transcriptional Regulatory Network from Gene Expression Data Using Nonlinear Manifold Embedding," PLOS ONE, Public Library of Science, vol. 6(8), pages 1-7, August.
    3. Guido Zampieri & Supreeta Vijayakumar & Elisabeth Yaneske & Claudio Angione, 2019. "Machine and deep learning meet genome-scale metabolic modeling," PLOS Computational Biology, Public Library of Science, vol. 15(7), pages 1-24, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Léon Faure & Bastien Mollet & Wolfram Liebermeister & Jean-Loup Faulon, 2023. "A neural-mechanistic hybrid approach improving the predictive power of genome-scale metabolic models," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    2. Wang, Wenjia & Zhou, Yi-Hui, 2021. "Eigenvector-based sparse canonical correlation analysis: Fast computation for estimation of multiple canonical vectors," Journal of Multivariate Analysis, Elsevier, vol. 185(C).
    3. Jose A Seoane & Colin Campbell & Ian N M Day & Juan P Casas & Tom R Gaunt, 2014. "Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery," PLOS Computational Biology, Public Library of Science, vol. 10(10), pages 1-13, October.
    4. Lee Woojoo & Lee Donghwan & Lee Youngjo & Pawitan Yudi, 2011. "Sparse Canonical Covariance Analysis for High-throughput Data," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 10(1), pages 1-24, July.
    5. Coleman Jacob & Replogle Joseph & Chandler Gabriel & Hardin Johanna, 2016. "Resistant multiple sparse canonical correlation," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 15(2), pages 123-138, April.
    6. Tenenhaus, Arthur & Philippe, Cathy & Frouin, Vincent, 2015. "Kernel Generalized Canonical Correlation Analysis," Computational Statistics & Data Analysis, Elsevier, vol. 90(C), pages 114-131.
    7. Dmitry Kobak & Yves Bernaerts & Marissa A. Weis & Federico Scala & Andreas S. Tolias & Philipp Berens, 2021. "Sparse reduced‐rank regression for exploratory visualisation of paired multivariate data," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 70(4), pages 980-1000, August.
    8. Iaci, Ross & Sriram, T.N., 2013. "Robust multivariate association and dimension reduction using density divergences," Journal of Multivariate Analysis, Elsevier, vol. 117(C), pages 281-295.
    9. Chalise, Prabhakar & Fridley, Brooke L., 2012. "Comparison of penalty functions for sparse canonical correlation analysis," Computational Statistics & Data Analysis, Elsevier, vol. 56(2), pages 245-254.
    10. Diptavo Dutta & Yuan He & Ashis Saha & Marios Arvanitis & Alexis Battle & Nilanjan Chatterjee, 2022. "Aggregative trans-eQTL analysis detects trait-specific target gene sets in whole blood," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    11. Ronglai Shen & Qianxing Mo & Nikolaus Schultz & Venkatraman E Seshan & Adam B Olshen & Jason Huse & Marc Ladanyi & Chris Sander, 2012. "Integrative Subtype Discovery in Glioblastoma Using iCluster," PLOS ONE, Public Library of Science, vol. 7(4), pages 1-9, April.
    12. Bin Li & Hyunjin Shin & Georgy Gulbekyan & Olga Pustovalova & Yuri Nikolsky & Andrew Hope & Marina Bessarabova & Matthew Schu & Elona Kolpakova-Hart & David Merberg & Andrew Dorner & William L Trepicc, 2015. "Development of a Drug-Response Modeling Framework to Identify Cell Line Derived Translational Biomarkers That Can Predict Treatment Outcome to Erlotinib or Sorafenib," PLOS ONE, Public Library of Science, vol. 10(6), pages 1-20, June.
    13. Langworthy, Benjamin W. & Stephens, Rebecca L. & Gilmore, John H. & Fine, Jason P., 2021. "Canonical correlation analysis for elliptical copulas," Journal of Multivariate Analysis, Elsevier, vol. 183(C).
    14. Yunfeng Zhang & Irina Gaynanova, 2022. "Joint association and classification analysis of multi‐view data," Biometrics, The International Biometric Society, vol. 78(4), pages 1614-1625, December.
    15. Sandra E. Safo & Eun Jeong Min & Lillian Haine, 2022. "Sparse linear discriminant analysis for multiview structured data," Biometrics, The International Biometric Society, vol. 78(2), pages 612-623, June.
    16. Bayarbaatar Amgalan & Hyunju Lee, 2014. "WMAXC: A Weighted Maximum Clique Method for Identifying Condition-Specific Sub-Network," PLOS ONE, Public Library of Science, vol. 9(8), pages 1-10, August.
    17. Zhang Fan & Miecznikowski Jeffrey C. & Tritchler David L., 2020. "Identification of supervised and sparse functional genomic pathways," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 19(1), pages 1-27, February.
    18. Jung, Sungkyu, 2018. "Continuum directions for supervised dimension reduction," Computational Statistics & Data Analysis, Elsevier, vol. 125(C), pages 27-43.
    19. Efrat Muller & Itamar Shiryan & Elhanan Borenstein, 2024. "Multi-omic integration of microbiome data for identifying disease-associated modules," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    20. Palzer, Elise F. & Wendt, Christine H. & Bowler, Russell P. & Hersh, Craig P. & Safo, Sandra E. & Lock, Eric F., 2022. "sJIVE: Supervised joint and individual variation explained," Computational Statistics & Data Analysis, Elsevier, vol. 175(C).

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1007677. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.