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. 2023 Feb 3;3:10. doi: 10.1038/s43705-022-00210-8

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© The Author(s) 2023

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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Fig. 1 — The vSAG1.JdFR (28 scaffolds) and vSAG8.JdFR (33 scaffolds). Black tick marks denote the breaks between the concatenated (using 10 Ns) scaffolds. The lines between the vSAG1.JdFR and vSAG8.JdFR genomes represent the nucleotide level alignment based on tBlastx analysis (alignment ranging from 16 to 100%). The predicted genes were assigned taxonomic affiliation based on Blastp analysis. Genes affiliated to bacteria (blue), archaea (orange), NCLDV (green), eukaryotes (gray), fungal (red), and scaffolds (black) for vSAG1.JdFR and vSAG8.JdFR on the genome.

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