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. 2019 Oct 14;8(10):1253. doi: 10.3390/cells8101253

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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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The data forming the Venn data in Figure 1 were analysed by the Bioconductor ReactomePA software package [30] to generate gene ontology (GO; y-axis) maps for significant F/R (a), I942 (b) and shared (c) genes. The x-axis represents the ratio of genes in the ontology over the total number of enriched genes. The occurrence of individual gene ontologies (count) and significance (p-adjust) are also displayed, as indicated in the key on the right of the graphs.

The data forming the Venn data in Figure 1 were analysed by the Bioconductor ReactomePA software package [30] to generate gene ontology (GO; y-axis) maps for significant F/R (a), I942 (b) and shared (c) genes. The x-axis represents the ratio of genes in the ontology over the total number of enriched genes. The occurrence of individual gene ontologies (count) and significance (p-adjust) are also displayed, as indicated in the key on the right of the graphs.