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. 2021 Feb 9;12:5. doi: 10.1186/s13100-021-00233-3

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© The Author(s) 2021

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. 5 — Scatter plots comparing ORF1p IP RNAs, granules RNAs and RNAs correlated with LINE-1 in TCGA prostate cancer. a For each gene, enrichment in p-body purification study [55] (x-axis) vs enrichment in our ORF1p IPs, calculated by DESeq2 (y-axis). b Same y-axis as in a, but using SG enrichments [54] on the x-axis. c RNA expression correlation between host genes and intact LINE-1 in TCGA prostate cancer samples (x-axis) vs enrichment in our ORF1p IPs (y-axis). d Same x-axis as in c, but y-axis is p-body enrichment (same as x-axis in a)