One key exploratory analysis step in single-cell genomics data analysis is the prediction of features with different activity levels. For example, we want to predict differentially expressed genes (DEGs) in single-cell RNA-seq data, spatial DEGs in spatial transcriptomics data, or differentially accessible regions (DARs) in single-cell ATAC-seq data. 'singleCellHaystack' predicts differentially active features in single cell omics datasets without relying on the clustering of cells into arbitrary clusters. 'singleCellHaystack' uses Kullback-Leibler divergence to find features (e.g., genes, genomic regions, etc) that are active in subsets of cells that are non-randomly positioned inside an input space (such as 1D trajectories, 2D tissue sections, multi-dimensional embeddings, etc). For the theoretical background of 'singleCellHaystack' we refer to our original paper Vandenbon and Diez (Nature Communications, 2020) <doi:10.1038/s41467-020-17900-3> and our update Vandenbon and Diez (bioRxiv, 2022) <doi:10.1101/2022.11.13.516355>.
Package details |
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Author | Alexis Vandenbon [aut, cre] (<https://orcid.org/0000-0003-2180-5732>), Diego Diez [aut] (<https://orcid.org/0000-0002-2325-4893>) |
Maintainer | Alexis Vandenbon <alexis.vandenbon@gmail.com> |
License | MIT + file LICENSE |
Version | 1.0.0 |
Package repository | View on CRAN |
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