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. 2020 Feb 5;3:56. doi: 10.1038/s42003-019-0741-7

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© The Author(s) 2020, corrected publication 2022

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. 2 — a Proportional Venn diagrams displaying the overlap between CLC set and the three indicated databases. Shown are the total numbers of unique human lncRNAs contained in each intersection (note that for LncRNADisease, numbers refer only to cancer-related genes). Databases are divided into genes that belong to GENCODE v24 annotation and others. b Barplot shows the percent of GENCODE v24 lncRNAs of each database that is present in the final list of cancer lncRNA candidates of two CRISPR/Cas-9 cancer screenings (Liu et al.⁹ and Zhu et al.⁴⁷). N represents the number of GENCODE v24 lncRNAs from each database that were tested in each of the two CRISPR/Cas-9 screenings. Names of the genes that overlap between the databases and the screenings are shown in each bar. p-values were calculated using Fisher’s exact test.