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>.
https://anaconda.org/r/r-ioncopy/badges/version.svg
https://anaconda.org/r/r-ioncopy/badges/latest_release_date.svg
https://anaconda.org/r/r-ioncopy/badges/latest_release_relative_date.svg
https://anaconda.org/r/r-ioncopy/badges/platforms.svg
https://anaconda.org/r/r-ioncopy/badges/license.svg
https://anaconda.org/r/r-ioncopy/badges/downloads.svg