4.8 Article

Model-free prediction test with application to genomics data

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2205518119

关键词

prediction test; sample splitting; machine learning; CITE-seq data; spatially variable genes

资金

  1. NSF at the Pittsburgh Supercomputing Center [DMS-2015492, OAC-1928147]
  2. National Institute of Mental Health (NIMH) [R01MH123184]

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This paper introduces a method for testing the significance of predictors in a regression model under the model-free setting. It assumes that the predictors do not significantly contribute to the prediction of the outcome given confounding variables. By using nonparametric machine learning regression algorithms and comparing the prediction power of different models, the test results can be obtained. The method has important biological implications in gene expression data analysis.
Testing the significance of predictors in a regression model is one of the most important topics in statistics. This problem is especially difficult without any parametric assumptions on the data. This paper aims to test the null hypothesis that given confounding variables Z, X does not significantly contribute to the prediction of Y under the model-free setting, where X and Z are possibly high dimensional. We propose a general framework that first fits nonparametricmachine learning regression algorithms onY|Z and Y|(X, Z), then compares the prediction power of the two models. The proposed method allows us to leverage the strength of the most powerful regression algorithms developed in the modern machine learning community. The P value for the test can be easily obtained by permutation. In simulations, we find that the proposed method is more powerful compared to existing methods. The proposed method allows us to draw biologically meaningful conclusions from two gene expression data analyses without strong distributional assumptions: 1) testing the prediction power of sequencing RNA for the proteins in cellular indexing of transcriptomes and epitopes by sequencing data and 2) identification of spatially variable genes in spatially resolved transcriptomics data.

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