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. 2023 Mar 27;24:148. doi: 10.1186/s12864-023-09255-y

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© The Author(s) 2023

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. 2 — HiFi assemblies showed twofold higher contiguity than depth-matched CLR assemblies. A Nx plot showing the distribution of contig lengths in each assembly. The intersection of each horizontal solid line and vertical dotted line indicates the N50 of each assembly. B BUSCO values of each assembly. Note that the reference genome CB4856 was also built on CLR rather than HiFi. C Lengths of the ribosomal RNA sequences in each assembly and their previously estimated lengths in C. elegans