Effective and scalable single-cell data alignment with non-linear canonical correlation analysis

Author:

Hu Jialu1,Chen Mengjie2,Zhou Xiang13ORCID

Affiliation:

1. Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA

2. Department of Human Genetics and Department of Medicine, University of Chicago, Chicago, IL 60637, USA

3. Center for Statistical Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Abstract

Abstract Data alignment is one of the first key steps in single cell analysis for integrating multiple datasets and performing joint analysis across studies. Data alignment is challenging in extremely large datasets, however, as the major of the current single cell data alignment methods are not computationally efficient. Here, we present VIPCCA, a computational framework based on non-linear canonical correlation analysis for effective and scalable single cell data alignment. VIPCCA leverages both deep learning for effective single cell data modeling and variational inference for scalable computation, thus enabling powerful data alignment across multiple samples, multiple data platforms, and multiple data types. VIPCCA is accurate for a range of alignment tasks including alignment between single cell RNAseq and ATACseq datasets and can easily accommodate millions of cells, thereby providing researchers unique opportunities to tackle challenges emerging from large-scale single-cell atlas.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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