BioinformaticsBioinformaticsPeer-reviewed journal article
SCAN-ATAC Sim: a scalable and efficient method for simulating single-cell ATAC-seq from bulk-tissue experiments
Zhanlin CheniD, Jing ZhangiD, Jason J. LiuiD, Zixuan ZhangiD, Jiangqi Zhu, Donghoon LeeiD, Min XuiD, Mark GersteiniD
Abstract
SummaryscATAC-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. AvailabilitySCAN-ATAC-Sim is available at scan-atac-sim.gersteinlab.org. Contactpi@gersteinlab.org Supplementary informationSupplementary data are available at Bioinformatics online.
- assay: scATAC-seq
- assay: bulk RNA-seq
- research focus: benchmarking
- research focus: database / resource
- research focus: software / tool
- approach: simulation
- Citations
- 15
- FWCI
- 0.63
- Field percentile
- top 40%
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