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Conumee 2.0: enhanced copy-number variation analysis from DNA methylation arrays for humans and mice

17 Jan 2024

Abstract excerpt

MOTIVATION: Copy-number variations (CNVs) are common genetic alterations in cancer and their detection may impact tumor classification and therapeutic decisions. However, detection of clinically relevant large and focal CNVs remains challenging when sample material or resources are limited. This has motivated us to create a software tool to infer CNVs from DNA methylation arrays which are often generated as part...

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PMID: 38244574
DOI: 10.1093/bioinformatics/btae029

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