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. 2018 Feb 2;32(7):1561–1566. doi: 10.1038/s41375-018-0017-0

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a Genomic HRD-LOH across all myeloma samples with those carrying a mutation in a gene associated with homologous recombination indicated in black (HRmut). b Genomic HRD-LOH by presence of HRmut or wild type (HRwt). Wilcoxon test for difference between groups, p = 0.056. c Genomic HRD-LOH by presence of a BRCA1/2 mutation. Wilcoxon test for difference between groups, p = 0.383. The raw data points and the median and inter-quartile range for each data set are shown. The number and percentage of patients with a mutation identified in each of the genes indicated is shown in the table below the figure