DeAnnCNV (Detection and Annotation of Copy Number Variations) is a web-based tool to detect and annotate copy number variation (CNV) in whole genome exome sequencing. The algorithm is based on GPHMM tool (see links).
Genomics; Sequence analysis; DNA structural variation
Zhang Y, Yu Z, Ban R, Zhang H, Iqbal F, Zhao A, Li A, Shi Q "DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing data." Nucleic Acids Res. 2015 Jul 1;43(W1):W289-94. Epub 2015 May 26. https://doi.org/10.1093/nar/gkv556
PMID: 26013811
PMCID: PMC4489280
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