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. Budczies (2016 Mar 15) <doi:10.18632/oncotarget.7451>.
|Author||Jan Budczies, Eva Romanovsky|
|Maintainer||Jan Budczies <firstname.lastname@example.org>|
|Package repository||View on CRAN|
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