期刊
CELL REPORTS METHODS
卷 2, 期 3, 页码 -出版社
CELL PRESS
DOI: 10.1016/j.crmeth.2022.100182
关键词
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资金
- Chan Zuckerberg Foundation Network [2019-02452]
- NIH-NIAID [U19 AI090023]
In this study, a probabilistic framework called PeakVI is presented, which leverages deep neural networks to analyze scATAC-seq data. The framework fits an informative latent space that preserves biological heterogeneity while correcting batch effects and accounting for technical effects. PeakVI also provides a technique for identifying differential accessibility at a single-region resolution, enabling cell-type annotation and identification of key cis-regulatory elements.
Single-cell ATAC sequencing (scATAC-seq) is a powerful and increasingly popular technique to explore the regulatory landscape of heterogeneous cellular populations. However, the high noise levels, degree of sparsity, and scale of the generated data make its analysis challenging. Here, we present PeakVI, a probabilistic framework that leverages deep neural networks to analyze scATAC-seq data. PeakVI fits an informative latent space that preserves biological heterogeneity while correcting batch effects and accounting for technical effects, such as library size and region-specific biases. In addition, PeakVI provides a technique for identifying differential accessibility at a single-region resolution, which can be used for cell-type annotation as well as identification of key cis-regulatory elements. We use public datasets to demonstrate that PeakVI is scalable, stable, robust to low-quality data, and outperforms current analysis methods on a range of critical analysis tasks. PeakVI is publicly available and implemented in the scvi-tools framework.
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