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. 2018 Mar 7;8:4124. doi: 10.1038/s41598-018-22284-y

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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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UCSC genome browser tracks visualization for the DAS events in Exoc1/EXOC1 and Fbln2/FBLN2. The bigWigs UCSC genome browser tracks of the mapped reads in mice and humans were generated to visualize DAS events. To increase interpretability for the human psoriasis dataset, mapped reads were collapsed within groups of lesional psoriatic samples (P) and normal skin samples (N). The figures depict the expanded regions spanning over splicing events in the UCSC genome browser. (a) Visualization of the DAS event in Exoc1/EXOC1. The psoriatic samples have more inclusion of variable exons in both mice and humans. (b) Visualization of the DAS event in Fbln2/FBLN2. The psoriatic samples have less inclusion of variable exons in both mice and humans.