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. 2016 Jan 20;12:2. doi: 10.1186/s13007-016-0107-9

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© Visendi et al. 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. 3 — BES mappings on contigs of simulated pool (ABCE). Clones A, C and E have forward (M13_For) and reverse (SP6_Rev) BES (A01_M13_For, A01_SP6_Rev, C01_M13_For, C01_SP6_Rev, E01_M13_For, E01_SP6_Rev) respectively correctly mapped. Clone B had no BES available but 120 bp sequences from cloning vector ends (FOR and REV) were used to identify contig ends of clone B