ELLIPSIS: robust quantification of splicing in scRNA-seq.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39936571.
- Also identified by DOI 10.1093/bioinformatics/btaf028 and PMC identifier 11878791.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Alternative splicing is a tightly regulated biological process, that due to its cell type specific behavior, calls for analysis at the single cell level. However, quantifying differential splicing in scRNA-seq is challenging due to low and uneven coverage. Hereto, we developed ELLIPSIS, a tool for robust quantification of splicing in scRNA-seq that leverages locally observed read coverage with conservation of flow and intra-cell type similarity properties. Additionally, it is also able to quantify splicing in novel splicing events, which is extremely important in cancer cells where lots of novel splicing events occur. Application of ELLIPSIS to simulated data proves that our method is able to robustly estimate Percent Spliced In values in simulated data, and allows to reliably detect differential splicing between cell types. Using ELLIPSIS on glioblastoma scRNA-seq data, we identified genes that are differentially spliced between cancer cells in the tumor core and infiltrating cancer cells found in peripheral tissue. These genes showed to play a role in a.o. cell migration and motility, cell projection organization, and neuron projection guidance. ELLIPSIS quantification tool: https://github.com/MarchalLab/ELLIPSIS.git.
Medical subject headings
- Alternative Splicing
- Single-Cell Analysis
- Software
- RNA-Seq
- Sequence Analysis, RNA
- RNA Splicing