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CView: A network based tool for enhanced alignment visualization

View ORCID ProfileRaquel Linheiro, View ORCID ProfileDiana Lobo, View ORCID ProfileStephen Sabatino, View ORCID ProfileJohn Archer
doi: https://doi.org/10.1101/2022.01.17.476623
Raquel Linheiro
1, Vairão, Portugal
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Diana Lobo
1, Vairão, Portugal
2Departamento de Biologia, Faculdade de Ciências, Universidade do Porto, Porto, Portugal
3BIOPOLIS, Program in Genomics, Biodiversity and Land Planning, CIBIO, Campus de Vairão, Vairão, Portugal
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Stephen Sabatino
1, Vairão, Portugal
3BIOPOLIS, Program in Genomics, Biodiversity and Land Planning, CIBIO, Campus de Vairão, Vairão, Portugal
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John Archer
1, Vairão, Portugal
3BIOPOLIS, Program in Genomics, Biodiversity and Land Planning, CIBIO, Campus de Vairão, Vairão, Portugal
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  • For correspondence: john.archer@cibio.up.pt
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Abstract

To date basic visualization of sequence alignments have largely focused on displaying per-site columns of nucleotide, or amino acid, residues along with associated frequency summarizations. The persistence of this tendency to the more recent tools designed for the viewing of mapped read data indicates that such a perspective not only provides a reliable visualization of per-site alterations, but also offers implicit reassurance to the end user in relation to data accessibility. However, the initial insight gained is limited, something that is especially true when viewing alignments consisting of many sequences representing differing factors, such as geographical location, date and subtype. A basic alignment viewer can have potential to increase initial insight through visual enhancement, whilst not delving into the realms of complex sequence analysis. Here we present CView, a visualizer that expands on the per-site representation of residues through the incorporation of a dynamic network that is based on the summarization of diversity present across different regions of the alignment. Within the network nodes are based on the clustering of sequence fragments spanning windows that are placed consecutively along the alignment. Edges are placed between nodes of neighbouring windows where they share sequence id’s. Thus, if a single node is selected on the network, then the relationship that all sequences passing through that node have to other regions of diversity within the alignment can be instantly observed through the tracing of paths. In addition to augmenting visual insight, CView provides many export features including variant summarization, per-site residue and kmer frequency matrixes, consensus sequence generation, alignment dissection as well as general sequence clustering, each of which are useful across a range of research areas. The software has been designed to be user friendly, intuitive and interactive. It, along with source code, a quick start guide and test data, are available through the SourceForge project page: https://sourceforge.net/projects/cview/.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted January 20, 2022.
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CView: A network based tool for enhanced alignment visualization
Raquel Linheiro, Diana Lobo, Stephen Sabatino, John Archer
bioRxiv 2022.01.17.476623; doi: https://doi.org/10.1101/2022.01.17.476623
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CView: A network based tool for enhanced alignment visualization
Raquel Linheiro, Diana Lobo, Stephen Sabatino, John Archer
bioRxiv 2022.01.17.476623; doi: https://doi.org/10.1101/2022.01.17.476623

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