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SCAN-ATAC-Sim: a scalable and efficient method for simulating single-cell ATAC-seq data from bulk-tissue experiments

View ORCID ProfileZhanlin Chen, Jing Zhang, Jason Liu, Zixuan Zhang, Jiangqi Zhu, Donghoon Lee, Min Xu, Mark Gerstein
doi: https://doi.org/10.1101/2020.05.29.123638
Zhanlin Chen
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA
2Department of Computer Science, Yale University, New Haven, CT 06520, USA
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  • ORCID record for Zhanlin Chen
Jing Zhang
3Department of Computer Science, University of California, Irvine, CA 92617, USA
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  • For correspondence: pi@gersteinlab.org
Jason Liu
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA
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Zixuan Zhang
4School of Electronic Engineering and Computer Science, Queen Mary University of London, London E1 4NS, United Kingdom
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Jiangqi Zhu
4School of Electronic Engineering and Computer Science, Queen Mary University of London, London E1 4NS, United Kingdom
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Donghoon Lee
5Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
6Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
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Min Xu
7Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA 15213, USA
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Mark Gerstein
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA
2Department of Computer Science, Yale University, New Haven, CT 06520, USA
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  • For correspondence: pi@gersteinlab.org
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Abstract

Summary scATAC-seq is a powerful approach for characterizing cell-type-specific regulatory landscapes. However, it is difficult to benchmark the performance of various scATAC-seq analysis techniques (such as clustering and deconvolution) without having a priori a known set of gold-standard cell types. To simulate scATAC-seq experiments with known cell-type labels, we introduce an efficient and scalable scATAC-seq simulation method (SCAN-ATAC-Sim) that down-samples bulk ATAC-seq data (e.g., from representative cell lines or tissues). Our protocol uses a consistent but tunable signal-to-noise ratio across cell types in a scATAC-seq simulation for integrating bulk experiments with different levels of background noise, and it independently samples twice without replacement to account for the diploid genome. Because it uses an efficient weighted reservoir sampling algorithm and is highly parallelizable with OpenMP, our implementation in C++ allows millions of cells to be simulated in less than an hour on a laptop computer.

Availability SCAN-ATAC-Sim is available at scan-atac-sim.gersteinlab.org.

Contact pi{at}gersteinlab.org

Supplementary information Supplementary data are available at Bioinformatics online.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • We have modified our figure and added results validating the simulations.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted November 03, 2020.
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SCAN-ATAC-Sim: a scalable and efficient method for simulating single-cell ATAC-seq data from bulk-tissue experiments
Zhanlin Chen, Jing Zhang, Jason Liu, Zixuan Zhang, Jiangqi Zhu, Donghoon Lee, Min Xu, Mark Gerstein
bioRxiv 2020.05.29.123638; doi: https://doi.org/10.1101/2020.05.29.123638
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SCAN-ATAC-Sim: a scalable and efficient method for simulating single-cell ATAC-seq data from bulk-tissue experiments
Zhanlin Chen, Jing Zhang, Jason Liu, Zixuan Zhang, Jiangqi Zhu, Donghoon Lee, Min Xu, Mark Gerstein
bioRxiv 2020.05.29.123638; doi: https://doi.org/10.1101/2020.05.29.123638

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