[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1009600.html
   My bibliography  Save this article

A copula based topology preserving graph convolution network for clustering of single-cell RNA-seq data

Author

Listed:
  • Snehalika Lall
  • Sumanta Ray
  • Sanghamitra Bandyopadhyay
Abstract
Annotation of cells in single-cell clustering requires a homogeneous grouping of cell populations. There are various issues in single cell sequencing that effect homogeneous grouping (clustering) of cells, such as small amount of starting RNA, limited per-cell sequenced reads, cell-to-cell variability due to cell-cycle, cellular morphology, and variable reagent concentrations. Moreover, single cell data is susceptible to technical noise, which affects the quality of genes (or features) selected/extracted prior to clustering.Here we introduce sc-CGconv (copula based graph convolution network for single clustering), a stepwise robust unsupervised feature extraction and clustering approach that formulates and aggregates cell–cell relationships using copula correlation (Ccor), followed by a graph convolution network based clustering approach. sc-CGconv formulates a cell-cell graph using Ccor that is learned by a graph-based artificial intelligence model, graph convolution network. The learned representation (low dimensional embedding) is utilized for cell clustering. sc-CGconv features the following advantages. a. sc-CGconv works with substantially smaller sample sizes to identify homogeneous clusters. b. sc-CGconv can model the expression co-variability of a large number of genes, thereby outperforming state-of-the-art gene selection/extraction methods for clustering. c. sc-CGconv preserves the cell-to-cell variability within the selected gene set by constructing a cell-cell graph through copula correlation measure. d. sc-CGconv provides a topology-preserving embedding of cells in low dimensional space.Author summary: One of the important aspects of single cell downstream analysis is to classify cells into subpopulations. This immediately leads to clustering of cells into homogeneous groups, which faces lots of issues due to (i) small amount of starting RNA, (ii) cell-to-cell variability, (iii) technical noise incorporated within the single cell sequencing technology, and (iv) unavailability of discriminating selected/extracted genes (features) in the preprocessing step of downstream analysis. We proposed sc-CGconv, stepwise feature extraction and clustering framework, which leverage landmark advantage of copula and graph convolution network in single-cell analysis domain. sc-CGconv outperforms the state-of-the-art feature selection/extraction methods in the preprocessing steps, performs well with small sample size data, can preserve the cell-to-cell variability within the extracted features, provides a topology-preserving embedding of cells in low dimensional space. sc-CGconv therefore successfully addresses the above-mentioned key challenges.

Suggested Citation

  • Snehalika Lall & Sumanta Ray & Sanghamitra Bandyopadhyay, 2022. "A copula based topology preserving graph convolution network for clustering of single-cell RNA-seq data," PLOS Computational Biology, Public Library of Science, vol. 18(3), pages 1-16, March.
  • Handle: RePEc:plo:pcbi00:1009600
    DOI: 10.1371/journal.pcbi.1009600
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1009600
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1009600&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1009600?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. Grace X. Y. Zheng & Jessica M. Terry & Phillip Belgrader & Paul Ryvkin & Zachary W. Bent & Ryan Wilson & Solongo B. Ziraldo & Tobias D. Wheeler & Geoff P. McDermott & Junjie Zhu & Mark T. Gregory & Jo, 2017. "Massively parallel digital transcriptional profiling of single cells," Nature Communications, Nature, vol. 8(1), pages 1-12, April.
    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. Qunlun Shen & Shihua Zhang, 2021. "Approximate distance correlation for selecting highly interrelated genes across datasets," PLOS Computational Biology, Public Library of Science, vol. 17(11), pages 1-18, November.
    2. Jinzhou Li & Marloes H. Maathuis, 2021. "GGM knockoff filter: False discovery rate control for Gaussian graphical models," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 83(3), pages 534-558, July.
    3. Lin Lin & Wei Shi & Jianbo Ye & Jia Li, 2023. "Multisource single‐cell data integration by MAW barycenter for Gaussian mixture models," Biometrics, The International Biometric Society, vol. 79(2), pages 866-877, June.

    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:pcbi00:1009600. 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.