Classifying cells with Scasat, a single-cell ATAC-seq analysis tool. Issue 2 (18th October 2018)

• Record Type: Journal Article
• Authors: Baker, Syed Murtuza; Rogerson, Connor; Hayes, Andrew; Sharrocks, Andrew D; Rattray, Magnus
• Is Part Of: Nucleic acids research. Volume 47:Issue 2(2019)
• Page Start: e10
• Page End: e10
• Publication Date: 2018-10-18
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gky950
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: ATAC-seq is a recently developed method to identify the areas of open chromatin in a cell. These regions usually correspond to active regulatory elements and their location profile is unique to a given cell type. When done at single-cell resolution, ATAC-seq provides an insight into the cell-to-cell variability that emerges from otherwise identical DNA sequences by identifying the variability in the genomic location of open chromatin sites in each of the cells. This paper presents Scasat (single-cell ATAC-seq analysis tool), a complete pipeline to process scATAC-seq data with simple steps. Scasat treats the data as binary and applies statistical methods that are especially suitable for binary data. The pipeline is developed in a Jupyter notebook environment that holds the executable code along with the necessary description and results. It is robust, flexible, interactive and easy to extend. Within Scasat we developed a novel differential accessibility analysis method based on information gain to identify the peaks that are unique to a cell. The results from Scasat showed that open chromatin locations corresponding to potential regulatory elements can account for cellular heterogeneity and can identify regulatory regions that separates cells from a complex population.