Transfer learning efficiently maps bone marrow cell types from mouse to human using single-cell RNA sequencing

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作者
Patrick S. Stumpf
Xin Du
Haruka Imanishi
Yuya Kunisaki
Yuichiro Semba
Timothy Noble
Rosanna C. G. Smith
Matthew Rose-Zerili
Jonathan J. West
Richard O. C. Oreffo
Katayoun Farrahi
Mahesan Niranjan
Koichi Akashi
Fumio Arai
Ben D. MacArthur
机构
[1] University of Southampton,Centre for Human Development, Stem Cells and Regeneration, Faculty of Medicine
[2] RWTH Aachen University,Joint Research Center for Computational Biomedicine
[3] University of Southampton,Electronics and Computer Sciences
[4] Kyushu University,Kyushu University, Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences
[5] Kyushu University Hospital,Center for Cellular and Molecular Medicine
[6] Kyushu University Graduate School of Medical Sciences,Department of Medicine and Biosystemic Science
[7] University of Southampton,Cancer Sciences, Faculty of Medicine
[8] University of Southampton,Institute for Life Sciences
[9] University of Southampton,Mathematical Sciences
[10] The Alan Turing Institute,undefined
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Biomedical research often involves conducting experiments on model organisms in the anticipation that the biology learnt will transfer to humans. Previous comparative studies of mouse and human tissues were limited by the use of bulk-cell material. Here we show that transfer learning—the branch of machine learning that concerns passing information from one domain to another—can be used to efficiently map bone marrow biology between species, using data obtained from single-cell RNA sequencing. We first trained a multiclass logistic regression model to recognize different cell types in mouse bone marrow achieving equivalent performance to more complex artificial neural networks. Furthermore, it was able to identify individual human bone marrow cells with 83% overall accuracy. However, some human cell types were not easily identified, indicating important differences in biology. When re-training the mouse classifier using data from human, less than 10 human cells of a given type were needed to accurately learn its representation. In some cases, human cell identities could be inferred directly from the mouse classifier via zero-shot learning. These results show how simple machine learning models can be used to reconstruct complex biology from limited data, with broad implications for biomedical research.
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