Article

PanCNV-Explorer: A pan-cancer resource to analyze copy number variations

2024-09-24

Abstract excerpt

<h4>Introduction</h4> Copy number variations (CNVs) are structural genomic alterations that involve changes in the number of copies of specific DNA regions. These variations can include deletions, duplications, and more complex rearrangements, and play a critical role in cancer progression by amplifying oncogenes, deleting tumor suppressor genes, or altering other key genomic regions. Despite the importance of CNV...

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Literature Corpus work: 63bd6319-2baf-5371-a7bf-29b65e68e5c1
DOI: 10.1101/2024.09.23.24314206

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