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Open Access

Correction

Correction: Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants

  • Weronika Przybyła,
  • Kirsti Marie Gjersvoll Paulsen,
  • Charitra Kumar Mishra,
  • Ståle Nygård,
  • Solveig Engebretsen,
  • Ellen Ruud,
  • Gunhild Trøen,
  • Klaus Beiske,
  • Lars Oliver Baumbusch

In Table 6, the SCA region and protein change of the TTN gene in patient 1 are incorrect and the three variants that are classified by Mutation Assessor as tolerated not damaging should be removed. Please see the correct Table 6 and its caption here.

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Table 6. Genes with novel non-synonymous variants detected in primary tumor samples, predicted to be damaging by the MutationAssessor program, found in more than one patient.

SCA–structural chromosome abnormality; chromosome locations of each variant have been included; CNV–copy number variant; ampl–amplification, na–not available.

https://doi.org/10.1371/journal.pone.0306687.t001

Reference

  1. 1. Przybyła W, Gjersvoll Paulsen KM, Mishra CK, Nygård S, Engebretsen S, Ruud E, et al. (2022) Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PLoS ONE 17(8): e0273280. pmid:36037157

Citation: Przybyła W, Gjersvoll Paulsen KM, Mishra CK, Nygård S, Engebretsen S, Ruud E, et al. (2024) Correction: Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PLoS ONE 19(7): e0306687. https://doi.org/10.1371/journal.pone.0306687

Published: July 1, 2024

Copyright: © 2024 Przybyła et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.