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Distribution-Free Multisample Tests Based on Optimal Matchings With Applications to Single Cell Genomics

Author

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  • Somabha Mukherjee
  • Divyansh Agarwal
  • Nancy R. Zhang
  • Bhaswar B. Bhattacharya

Abstract

In this article, we propose a nonparametric graphical test based on optimal matching, for assessing the equality of multiple unknown multivariate probability distributions. Our procedure pools the data from the different classes to create a graph based on the minimum non-bipartite matching, and then utilizes the number of edges connecting data points from different classes to examine the closeness between the distributions. The proposed test is exactly distribution-free (the null distribution does not depend on the distribution of the data) and can be efficiently applied to multivariate as well as non-Euclidean data, whenever the inter-point distances are well-defined. We show that the test is universally consistent, and prove a distributional limit theorem for the test statistic under general alternatives. Through simulation studies, we demonstrate its superior performance against other common and well-known multisample tests. The method is applied to single cell transcriptomics data obtained from the peripheral blood, cancer tissue, and tumor-adjacent normal tissue of human subjects with hepatocellular carcinoma and non-small-cell lung cancer. Our method unveils patterns in how biochemical metabolic pathways are altered across immune cells in a cancer setting, depending on the tissue location. All of the methods described herein are implemented in the R package multicross. Supplementary materials for this article are available online.

Suggested Citation

  • Somabha Mukherjee & Divyansh Agarwal & Nancy R. Zhang & Bhaswar B. Bhattacharya, 2022. "Distribution-Free Multisample Tests Based on Optimal Matchings With Applications to Single Cell Genomics," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 117(538), pages 627-638, April.
  • Handle: RePEc:taf:jnlasa:v:117:y:2022:i:538:p:627-638
    DOI: 10.1080/01621459.2020.1791131
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