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. 2014 Oct 16;14:276. doi: 10.1186/s12870-014-0276-5

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© Robinson et al.; licensee BioMed Central Ltd. 2014

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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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Genomic DNA and RNA-Sequencing read coverage (y axis) for the region of chromosome 19 (x axis) including Potri.019G047300. (a) Read coverage of uniquely mapping genomic DNA reads from a male (blue, 229.1) and female (pink, 349.2) individual. Black arrows represent exons with arrow direction indicating strand. (b,c) Read coverage of uniquely mapping RNA-Sequencing reads for male (b, n = 8) and female (c, n = 9) individuals. The coloured line represents the average per base pair read coverage across all individuals with grey indicating ± two standard deviations.