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bioRxiv · 10.1101/2021.09.29.462469

ReadZS detects developmentally regulated RNA processing programs in single cell RNA-seq and defines subpopulations independent of gene expression

Abstract

RNA processing (RNAP), including splicing and alternative polyadenylation, is crucial to gene function and regulation, but methods to detect RNAP from single-cell RNA sequencing data are limited by reliance on pre-existing annotations, peak-calling heuristics, and collapsing measurements by cell type. We introduce ReadZS, the first annotation-free statistical approach to identify regulated RNAP in single cells. ReadZS discovers cell type-specific RNAP in the human lung and conserved, developmentally regulated RNAP in mammalian spermatogenesis - including global 3 UTR shortening in human spermatogenesis. ReadZS also discovers global 3 UTR lengthening in Arabidopsis root development, highlighting the usefulness of this method in under-annotated transcriptomes.

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BibTeXRIS

Meyer, E., Dehghannasiri, R., Chaung, K., Salzman, J.. 2021-10-01. ReadZS detects developmentally regulated RNA processing programs in single cell RNA-seq and defines subpopulations independent of gene expression. https://doi.org/10.1101/2021.09.29.462469

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