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. 2019 Sep 5;10(9):678. doi: 10.3390/genes10090678

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Recurrent somatic copy number alterations (sCNA) in R0 patients of TCGA-OV27 cohort. (A) Plot of G scores (defined as the amplitude of the copy number multiplied by its frequency across samples) calculated by Genomic Identification of Significant Targets in Cancer (GISTIC) for genomic regions recurrently amplified (red) or deleted (blue) in the TCGA-OV27 dataset, at an FDR < 0.1. (B) Barplot showing the frequency of samples positive for the recurrently amplified (left) or deleted (right) regions identified by GISTIC.