Fast clustering and cell-type annotation of scATAC data using pre-trained embeddings

Author:

LeRoy Nathan J12ORCID,Smith Jason P134ORCID,Zheng Guangtao5ORCID,Rymuza Julia1ORCID,Gharavi Erfaneh16ORCID,Brown Donald E67ORCID,Zhang Aidong256ORCID,Sheffield Nathan C1234568ORCID

Affiliation:

1. Center for Public Health Genomics, School of Medicine, University of Virginia , Charlottesville, VA 22908, USA

2. Department of Biomedical Engineering, School of Medicine, University of Virginia , Charlottesville, VA 22904, USA

3. Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia , Charlottesville, VA 22908, USA

4. Child Health Research Center, School of Medicine, University of Virginia , Charlottesville, VA 22908, USA

5. Department of Computer Science, School of Engineering, University of Virginia , Charlottesville, VA 22908, USA

6. School of Data Science, University of Virginia , Charlottesville, VA 22904, USA

7. Department of Systems and Information Engineering, University of Virginia , Charlottesville, VA 22908, USA

8. Department of Public Health Sciences, School of Medicine, University of Virginia , Charlottesville, VA 22908, USA

Abstract

Abstract Data from the single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) are now widely available. One major computational challenge is dealing with high dimensionality and inherent sparsity, which is typically addressed by producing lower dimensional representations of single cells for downstream clustering tasks. Current approaches produce such individual cell embeddings directly through a one-step learning process. Here, we propose an alternative approach by building embedding models pre-trained on reference data. We argue that this provides a more flexible analysis workflow that also has computational performance advantages through transfer learning. We implemented our approach in scEmbed, an unsupervised machine-learning framework that learns low-dimensional embeddings of genomic regulatory regions to represent and analyze scATAC-seq data. scEmbed performs well in terms of clustering ability and has the key advantage of learning patterns of region co-occurrence that can be transferred to other, unseen datasets. Moreover, models pre-trained on reference data can be exploited to build fast and accurate cell-type annotation systems without the need for other data modalities. scEmbed is implemented in Python and it is available to download from GitHub. We also make our pre-trained models available on huggingface for public use. scEmbed is open source and available at https://github.com/databio/geniml. Pre-trained models from this work can be obtained on huggingface: https://huggingface.co/databio.

Funder

National Institute of General Medical Sciences

National Human Genome Research Institute

Publisher

Oxford University Press (OUP)

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