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Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments

BACKGROUND: Base-By-Base is a Java-based multiple sequence alignment editor. It is capable of working with protein and DNA molecules, but many of its unique features relate to the manipulation of the genomes of large DNA viruses such as poxviruses, herpesviruses, baculoviruses and asfarviruses (1-40...

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Autores principales: Hillary, William, Lin, Song-Han, Upton, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348662/
https://www.ncbi.nlm.nih.gov/pubmed/22587754
http://dx.doi.org/10.1186/2042-5783-1-2
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author Hillary, William
Lin, Song-Han
Upton, Chris
author_facet Hillary, William
Lin, Song-Han
Upton, Chris
author_sort Hillary, William
collection PubMed
description BACKGROUND: Base-By-Base is a Java-based multiple sequence alignment editor. It is capable of working with protein and DNA molecules, but many of its unique features relate to the manipulation of the genomes of large DNA viruses such as poxviruses, herpesviruses, baculoviruses and asfarviruses (1-400 kb). The tool was built to serve as a platform for comparative genomics at the level of individual nucleotides. RESULTS: In version 2, BBB-v2, of Base-By-Base we have added a series of new features aimed at providing the bench virologist with a better platform to view, annotate and analyze these complex genomes. Although a poxvirus genome, for example, may be less than 200 kb, it probably encodes close to 200 proteins using multiple classes of promoters with frequent overlapping of promoters and coding sequences and even some overlapping of genes. The new features allow users to 1) add primer annotations or other data sets in batch mode, 2) export differences between sequences to other genome browsers, 3) compare multiple genomes at a single nucleotide level of detail, 4) create new alignments from subsets/subsequences of a very large master alignment and 5) allow display of summaries of deep RNA sequencing data sets on a genome sequence. CONCLUSION: BBB-v2 significantly improves the ability of virologists to work with genome sequences and provides a platform with which they can use a multiple sequence alignment as the basis for their own editable documents. Also, a .bbb document, with a variety of annotations in addition to the basic coding regions, can be shared among collaborators or made available to an entire research community. The program is available via Virology.ca using Java Web Start and is platform independent; the Java 1.5 virtual machine is required.
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spelling pubmed-33486622012-05-10 Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments Hillary, William Lin, Song-Han Upton, Chris Microb Inform Exp Research BACKGROUND: Base-By-Base is a Java-based multiple sequence alignment editor. It is capable of working with protein and DNA molecules, but many of its unique features relate to the manipulation of the genomes of large DNA viruses such as poxviruses, herpesviruses, baculoviruses and asfarviruses (1-400 kb). The tool was built to serve as a platform for comparative genomics at the level of individual nucleotides. RESULTS: In version 2, BBB-v2, of Base-By-Base we have added a series of new features aimed at providing the bench virologist with a better platform to view, annotate and analyze these complex genomes. Although a poxvirus genome, for example, may be less than 200 kb, it probably encodes close to 200 proteins using multiple classes of promoters with frequent overlapping of promoters and coding sequences and even some overlapping of genes. The new features allow users to 1) add primer annotations or other data sets in batch mode, 2) export differences between sequences to other genome browsers, 3) compare multiple genomes at a single nucleotide level of detail, 4) create new alignments from subsets/subsequences of a very large master alignment and 5) allow display of summaries of deep RNA sequencing data sets on a genome sequence. CONCLUSION: BBB-v2 significantly improves the ability of virologists to work with genome sequences and provides a platform with which they can use a multiple sequence alignment as the basis for their own editable documents. Also, a .bbb document, with a variety of annotations in addition to the basic coding regions, can be shared among collaborators or made available to an entire research community. The program is available via Virology.ca using Java Web Start and is platform independent; the Java 1.5 virtual machine is required. BioMed Central 2011-06-14 /pmc/articles/PMC3348662/ /pubmed/22587754 http://dx.doi.org/10.1186/2042-5783-1-2 Text en Copyright ©2011 Hillary et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hillary, William
Lin, Song-Han
Upton, Chris
Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title_full Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title_fullStr Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title_full_unstemmed Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title_short Base-By-Base version 2: single nucleotide-level analysis of whole viral genome alignments
title_sort base-by-base version 2: single nucleotide-level analysis of whole viral genome alignments
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348662/
https://www.ncbi.nlm.nih.gov/pubmed/22587754
http://dx.doi.org/10.1186/2042-5783-1-2
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