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

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

Resource type
Journal article
Creator (person)
Seaman, Josiah
Buggs, Richard J. A.
Date published
April 30, 2020
Abstract
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.
Journal title
Frontiers in Genetics
Volume
11
Article number
292
Publisher
Frontiers Media SA
eISSN
1664-8021
Official URL
https://www.frontiersin.org/articles/10.3389/fgene.2020.00292/full
Rights statement
In Copyright
Licence
https://creativecommons.org/licenses/by/4.0/
DOI
10.3389/fgene.2020.00292
Keywords
data visualization
genome alignment
comparative genomics
space filling curves
genome browser
genome assembly
nucleotide visualization
chromosome structural variants
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