FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
An Erratum on
FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
by Seaman, J., and Buggs, R. J. A. (2020). Front. Genet. 11:292. doi: 10.3389/fgene.2020.00292
Due to a production error, there was an error in affiliation 1. Instead of “Richmond, VA, United Kingdom,” it should be “Richmond, United Kingdom.”
The publisher apologizes for this mistake. The original article has been updated.
Keywords: data visualization, nucleotide visualization, genome assembly, genome browser, chromosome structural variants, genome alignment, comparative genomics, space filling curves
Citation: Frontiers Production Office (2020) Erratum: FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments. Front. Genet. 11:745. doi: 10.3389/fgene.2020.00745
Received: 19 June 2020; Accepted: 22 June 2020;
Published: 08 July 2020.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2020 Frontiers Production Office. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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