ACEseq - method to detect somatic copy number variations

ACESeq Workflow

ACEseq is a method to detect somatic copy number variations from matching tumor/control WGS data pairs. In addition to total copy numbers it provides allele-specific copy numbers as well as ploidy and tumor cell content estimates for the tumor sample. It is implemented as Roddy workflow.

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Funding: Continuing development, support, and maintenance partially funded by de.NBI