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. 2016 Jul 1;17:480. doi: 10.1186/s12864-016-2831-y

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 1 — Coverage per NoV genome position. Number reads (in log scale) that aligned with the corresponding NoV consensus sequence of OU1 (a), OU2 (b), OU3 (c), OU4 (d), SP1 (e) and SP2 (f). Solid and broken lines indicate the start of ORF2 and ORF3, respectively