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SeqTools: visual tools for manual analysis of sequence alignments
BACKGROUND: Manual annotation is essential to create high-quality reference alignments and annotation. Annotators need to be able to view sequence alignments in detail. The SeqTools package provides three tools for viewing different types of sequence alignment: Blixem is a many-to-one browser of pai...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724122/ https://www.ncbi.nlm.nih.gov/pubmed/26801397 http://dx.doi.org/10.1186/s13104-016-1847-3 |
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author | Barson, Gemma Griffiths, Ed |
author_facet | Barson, Gemma Griffiths, Ed |
author_sort | Barson, Gemma |
collection | PubMed |
description | BACKGROUND: Manual annotation is essential to create high-quality reference alignments and annotation. Annotators need to be able to view sequence alignments in detail. The SeqTools package provides three tools for viewing different types of sequence alignment: Blixem is a many-to-one browser of pairwise alignments, displaying multiple match sequences aligned against a single reference sequence; Dotter provides a graphical dot-plot view of a single pairwise alignment; and Belvu is a multiple sequence alignment viewer, editor, and phylogenetic tool. These tools were originally part of the AceDB genome database system but have been completely rewritten to make them generally available as a standalone package of greatly improved function. FINDINGS: Blixem is used by annotators to give a detailed view of the evidence for particular gene models. Blixem displays the gene model positions and the match sequences aligned against the genomic reference sequence. Annotators use this for many reasons, including to check the quality of an alignment, to find missing/misaligned sequence and to identify splice sites and polyA sites and signals. Dotter is used to give a dot-plot representation of a particular pairwise alignment. This is used to identify sequence that is not represented (or is misrepresented) and to quickly compare annotated gene models with transcriptional and protein evidence that putatively supports them. Belvu is used to analyse conservation patterns in multiple sequence alignments and to perform a combination of manual and automatic processing of the alignment. High-quality reference alignments are essential if they are to be used as a starting point for further automatic alignment generation. CONCLUSIONS: While there are many different alignment tools available, the SeqTools package provides unique functionality that annotators have found to be essential for analysing sequence alignments as part of the manual annotation process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-016-1847-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4724122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47241222016-01-24 SeqTools: visual tools for manual analysis of sequence alignments Barson, Gemma Griffiths, Ed BMC Res Notes Technical Note BACKGROUND: Manual annotation is essential to create high-quality reference alignments and annotation. Annotators need to be able to view sequence alignments in detail. The SeqTools package provides three tools for viewing different types of sequence alignment: Blixem is a many-to-one browser of pairwise alignments, displaying multiple match sequences aligned against a single reference sequence; Dotter provides a graphical dot-plot view of a single pairwise alignment; and Belvu is a multiple sequence alignment viewer, editor, and phylogenetic tool. These tools were originally part of the AceDB genome database system but have been completely rewritten to make them generally available as a standalone package of greatly improved function. FINDINGS: Blixem is used by annotators to give a detailed view of the evidence for particular gene models. Blixem displays the gene model positions and the match sequences aligned against the genomic reference sequence. Annotators use this for many reasons, including to check the quality of an alignment, to find missing/misaligned sequence and to identify splice sites and polyA sites and signals. Dotter is used to give a dot-plot representation of a particular pairwise alignment. This is used to identify sequence that is not represented (or is misrepresented) and to quickly compare annotated gene models with transcriptional and protein evidence that putatively supports them. Belvu is used to analyse conservation patterns in multiple sequence alignments and to perform a combination of manual and automatic processing of the alignment. High-quality reference alignments are essential if they are to be used as a starting point for further automatic alignment generation. CONCLUSIONS: While there are many different alignment tools available, the SeqTools package provides unique functionality that annotators have found to be essential for analysing sequence alignments as part of the manual annotation process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-016-1847-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-22 /pmc/articles/PMC4724122/ /pubmed/26801397 http://dx.doi.org/10.1186/s13104-016-1847-3 Text en © Barson and Griffiths. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Technical Note Barson, Gemma Griffiths, Ed SeqTools: visual tools for manual analysis of sequence alignments |
title | SeqTools: visual tools for manual analysis of sequence alignments |
title_full | SeqTools: visual tools for manual analysis of sequence alignments |
title_fullStr | SeqTools: visual tools for manual analysis of sequence alignments |
title_full_unstemmed | SeqTools: visual tools for manual analysis of sequence alignments |
title_short | SeqTools: visual tools for manual analysis of sequence alignments |
title_sort | seqtools: visual tools for manual analysis of sequence alignments |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724122/ https://www.ncbi.nlm.nih.gov/pubmed/26801397 http://dx.doi.org/10.1186/s13104-016-1847-3 |
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