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. 2020 Jun 24;20:268. doi: 10.1186/s12935-020-01359-9

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 8 — Significant enrichment analysis of GO and KEGG pathways of target genes correlated with RP11-357H14.17 in UCEC with Metascape. a–f Cellular component (a, b), molecular function (c, d) and biological process (e, f) enrichment analysis of RP11-357H14.17-ralated targets colored by P-value with bar graph and network (Top 20). g, h KEGG pathways enrichment analysis of RP11-357H14.17-related targets colored by P-value with bar graph and network (Top 20). i The PPI network formed by protein–protein interaction (PPI) network and the ten most significant MCODE components of RP11-357H14.17 target genes. GO: Gene Ontology; KEGG: Kyoto Encyclopedia of Genes and Genomes; MCODE: Molecular Complex Detection. Above results were colored by P-value, where terms containing more genes tend to have a more significant P-value