4.7 Article

iSMNN: batch effect correction for single-cell RNA-seq data via iterative supervised mutual nearest neighbor refinement

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 5, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab122

关键词

iterative refinement; batch effect correction; single-cell RNA-seq; mutual nearest neighbor

资金

  1. National Institute of Health [R01 HL129132, R01 GM105785, R01 HL139880, R01 HL139976, R01 HL128331, R01 HL144551]
  2. American Heart Association (AHA) [18CDA34110340, 15GRNT25530005, 18TPA34180058]

向作者/读者索取更多资源

Batch effect correction is crucial in integrative analysis of multiple single-cell RNA-sequencing data. The iterative supervised MNN (iSMNN) refinement approach presented in this study shows advantages in mixing cells of the same type across batches and facilitating the identification of differentially expressed genes. iSMNN proves to be a valuable method for integrating multiple scRNA-seq datasets for biological and medical studies at single-cell level.
Batch effect correction is an essential step in the integrative analysis of multiple single-cell RNA-sequencing (scRNA-seq) data. One state-of-the-art strategy for batch effect correction is via unsupervised or supervised detection of mutual nearest neighbors (MNNs). However, both types of methods only detect MNNs across batches of uncorrected data, where the large batch effects may affect the MNN search. To address this issue, we presented a batch effect correction approach via iterative supervised MNN (iSMNN) refinement across data after correction. Our benchmarking on both simulation and real datasets showed the advantages of the iterative refinement of MNNs on the performance of correction. Compared to popular alternative methods, our iSMNN is able to better mix the cells of the same cell type across batches. In addition, iSMNN can also facilitate the identification of differentially expressed genes (DEGs) that are relevant to the biological function of certain cell types. These results indicated that iSMNN will be a valuable method for integrating multiple scRNA-seq datasets that can facilitate biological and medical studies at single-cell level.

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