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CONICS integrates scRNA-seq with DNA sequencing to map gene expression to tumor sub-clones
- Müller, Sören;
- Cho, Ara;
- Liu, Siyuan J;
- Lim, Daniel A;
- Diaz, Aaron
- Editor(s): Kelso, Janet
Published Web Location
https://doi.org/10.1093/bioinformatics/bty316Abstract
Motivation
Single-cell RNA-sequencing (scRNA-seq) has enabled studies of tissue composition at unprecedented resolution. However, the application of scRNA-seq to clinical cancer samples has been limited, partly due to a lack of scRNA-seq algorithms that integrate genomic mutation data.Results
To address this, we present.Conics
COpy-Number analysis In single-Cell RNA-Sequencing. CONICS is a software tool for mapping gene expression from scRNA-seq to tumor clones and phylogenies, with routines enabling: the quantitation of copy-number alterations in scRNA-seq, robust separation of neoplastic cells from tumor-infiltrating stroma, inter-clone differential-expression analysis and intra-clone co-expression analysis.Availability and implementation
CONICS is written in Python and R, and is available from https://github.com/diazlab/CONICS.Supplementary information
Supplementary data are available at Bioinformatics online.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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