Method for the calculation of copy numbers and calling of copy number alterations. The algorithm uses coverage data from amplicon sequencing of a sample cohort as input. The method includes significance assessment, correction for multiple testing and does not depend on normal DNA controls.
|Date of publication||2015-08-26 14:53:52|
|Maintainer||Jan Budczies <[email protected]>|
|Package repository||View on CRAN|
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