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FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments

Researchers seldom look at naked genome assemblies: instead the attributes of DNA sequences are mediated through statistics, annotations and high level summaries. Here we present software that visualizes the bare sequences of whole genome assemblies in a zoomable interface. This can assist in detect...

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Detalles Bibliográficos
Autores principales: Seaman, Josiah, Buggs, Richard J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203487/
https://www.ncbi.nlm.nih.gov/pubmed/32425967
http://dx.doi.org/10.3389/fgene.2020.00292
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author Seaman, Josiah
Buggs, Richard J. A.
author_facet Seaman, Josiah
Buggs, Richard J. A.
author_sort Seaman, Josiah
collection PubMed
description Researchers seldom look at naked genome assemblies: instead the attributes of DNA sequences are mediated through statistics, annotations and high level summaries. Here we present software that visualizes the bare sequences of whole genome assemblies in a zoomable interface. This can assist in detection of chromosome architecture and contamination by the naked eye through changes in color patterns, in the absence of any other annotation. When available, annotations can be visualized alongside or on top of the naked sequence. Genome alignments can also be visualized, laying two genomes side by side in an alignment and highlighting their differences at nucleotide resolution. FluentDNA gives researchers direct visualization of whole genome assemblies, annotations and alignments, for quality control, hypothesis generation, and communicating results.
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spelling pubmed-72034872020-05-18 FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments Seaman, Josiah Buggs, Richard J. A. Front Genet Genetics Researchers seldom look at naked genome assemblies: instead the attributes of DNA sequences are mediated through statistics, annotations and high level summaries. Here we present software that visualizes the bare sequences of whole genome assemblies in a zoomable interface. This can assist in detection of chromosome architecture and contamination by the naked eye through changes in color patterns, in the absence of any other annotation. When available, annotations can be visualized alongside or on top of the naked sequence. Genome alignments can also be visualized, laying two genomes side by side in an alignment and highlighting their differences at nucleotide resolution. FluentDNA gives researchers direct visualization of whole genome assemblies, annotations and alignments, for quality control, hypothesis generation, and communicating results. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7203487/ /pubmed/32425967 http://dx.doi.org/10.3389/fgene.2020.00292 Text en Copyright © 2020 Seaman and Buggs. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Genetics
Seaman, Josiah
Buggs, Richard J. A.
FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title_full FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title_fullStr FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title_full_unstemmed FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title_short FluentDNA: Nucleotide Visualization of Whole Genomes, Annotations, and Alignments
title_sort fluentdna: nucleotide visualization of whole genomes, annotations, and alignments
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203487/
https://www.ncbi.nlm.nih.gov/pubmed/32425967
http://dx.doi.org/10.3389/fgene.2020.00292
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