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. 2020 Feb 26;21:183. doi: 10.1186/s12864-020-6597-x

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© The Author(s). 2020

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 — Specificity and percentage of totally selected pairs for the FRAGTE and TETRA approaches on simulated genomes. a for specificity of FRAGTE; b for specificity of TETRA; c for totally sieved pairs of FRAGTE; d for totally sieved pairs of TETRA. All were run on the 1779 queries against 264 references with 10–100% of genome completeness, totally comprising 469,656 pairs. The specificity (%) in cell is calculated using the number of correctly filtered interspecies pairs divided by the total number of interspecies pairs. The percentage of totally sieved pairs in cell is calculated using the total number of sieved pairs divided by the total number of pairs. The number in cell is used as a basis for color intensity