Archive Page: CnD

Archive Page: CnD


Archive page. This resource is no longer available at the Sanger Institute.


A copy number variant caller for inbred strains.

cnD is a program to detect copy number variants from short read sequence data.

The target organism is assumed to be inbred, and therefore homozygous, so regions of apparent heterozygous SNPs (as called by MAQ) can be used to detect copy number gains. cnD uses both the rate of these paralogous sequence variants, and the raw sequence depth, to call copy number gains and losses using a hidden markov model.


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Tool Type