Back to search

Article

Inferring copy number variation from gene expression data: methods, comparisons, and applications to oncology

2021-10-19

Abstract excerpt

<h4>ABSTRACT</h4> Copy number variations (CNVs) are genomic events where the number of copies of a particular gene varies from cell to cell. Cancer cells are associated with somatic CNV changes resulting in gene amplifications and gene deletions. However, short of single-cell whole-genome sequencing, it is difficult to detect and quantify CNV events in single cells. In contrast, the rapid development of single-ce...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
c74d881e-6317-5156-8df0-865fd290372f
DOI
10.1101/2021.10.18.463991
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Inferring copy number variation from gene expression data: methods, comparisons, and applications to oncologyDOI 10.1101/2021.10.18.463991
Select a neighboring publication to make it the new centre.