CONY: A Bayesian procedure for detecting copy number variations from sequencing read depths
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DOI: 10.1038/s41598-020-64353-1
Abstract: Copy number variations (CNVs) are genomic structural mutations consisting of abnormal numbers of fragment copies. Next-generation sequencing of read-depth signals mirrors these variants. Some tools used to predict CNVs by depth have been published, but… read more here.
Keywords: cony; sequencing read; copy number; number variations ... See more keywords