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.
Authors
- Martin Vingron (ORCID: https://orcid.org/0000-0002-1765-4241)
- Aybuge Altay (ORCID: https://orcid.org/0000-0001-7341-7091)
Institutions
- Max Planck Institute for Molecular Genetics (DE)
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
Funders
- Deutsche Forschungsgemeinschaft