scATAcat: cell-type annotation for scATAC-seq data

Cells whose accessibility landscape has been profiled with scATAC-seq cannot readily be annotated to a particular cell type. In fact, annotating cell-types in scATAC-seq data is a challenging task since, unlike in scRNA-seq data, we lack knowledge of 'marker regions' which could be used for cell-type annotation. Current annotation methods typically translate accessibility to expression space and rely on gene expression patterns. We propose a novel approach, scATAcat, that leverages characterized bulk ATAC-seq data as prototypes to annotate scATAC-seq data. To mitigate the inherent sparsity of single-cell data, we aggregate cells that belong to the same cluster and create pseudobulk. To demonstrate the feasibility of our approach we collected a number of datasets with respective annotations to quantify the results and evaluate performance for scATAcat. scATAcat is available as a python package at https://github.com/aybugealtay/scATAcat.

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Publication Details

Journal
NAR Genomics and Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/nargab/lqae135
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.23

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article

scATAcat: cell-type annotation for scATAC-seq data

Martin Vingron, Aybuge Altay
1 citations
NAR Genomics and Bioinformatics
Single-cell and spatial transcriptomics
0.23
article

scATAcat: cell-type annotation for scATAC-seq data

Martin Vingron, Aybuge Altay
article en
1 citations

Abstract

Cells whose accessibility landscape has been profiled with scATAC-seq cannot readily be annotated to a particular cell type. In fact, annotating cell-types in scATAC-seq data is a challenging task since, unlike in scRNA-seq data, we lack knowledge of 'marker regions' which could be used for cell-type annotation. Current annotation methods typically translate accessibility to expression space and rely on gene expression patterns. We propose a novel approach, scATAcat, that leverages characterized bulk ATAC-seq data as prototypes to annotate scATAC-seq data. To mitigate the inherent sparsity of single-cell data, we aggregate cells that belong to the same cluster and create pseudobulk. To demonstrate the feasibility of our approach we collected a number of datasets with respective annotations to quantify the results and evaluate performance for scATAcat. scATAcat is available as a python package at https://github.com/aybugealtay/scATAcat.

NAR Genomics and BioinformaticsVol. 6(4)
Max Planck Institute for Molecular Genetics (DE)
Deutsche Forschungsgemeinschaft
Life in Land
Openalex Percentile: Top 42%
Single-cell and spatial transcriptomics
0.23
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