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. 2021 Dec 16;22:902. doi: 10.1186/s12864-021-08220-x

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© The Author(s) 2021

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 — Mutations in the β-globin gene can be accurately phased across multiple exons due to long-read nanopore sequencing. Top: The c.92 + 1G > A variant in sample 144 is phased with the wild-type allele at the Glu7 residue. Centre and bottom: In both samples 245 and 462, the stop-gain variant is in phase with the wild-type allele at Glu7