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Making whole genome multiple alignments usable for biologists
Summary: Here we describe a set of tools implemented within the Galaxy platform designed to make analysis of multiple genome alignments truly accessible for biologists. These tools are available through both a web-based graphical user interface and a command-line interface. Availability and Implemen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157923/ https://www.ncbi.nlm.nih.gov/pubmed/21775304 http://dx.doi.org/10.1093/bioinformatics/btr398 |
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author | Blankenberg, Daniel Taylor, James Nekrutenko, Anton |
author_facet | Blankenberg, Daniel Taylor, James Nekrutenko, Anton |
author_sort | Blankenberg, Daniel |
collection | PubMed |
description | Summary: Here we describe a set of tools implemented within the Galaxy platform designed to make analysis of multiple genome alignments truly accessible for biologists. These tools are available through both a web-based graphical user interface and a command-line interface. Availability and Implementation: This open-source toolset was implemented in Python and has been integrated into the online data analysis platform Galaxy (public web access: http://usegalaxy.org; download: http://getgalaxy.org). Additional help is available as a live supplement from http://usegalaxy.org/u/dan/p/maf. Contact: james.taylor@emory.edu; anton@bx.psu.edu Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-3157923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31579232011-08-18 Making whole genome multiple alignments usable for biologists Blankenberg, Daniel Taylor, James Nekrutenko, Anton Bioinformatics Applications Note Summary: Here we describe a set of tools implemented within the Galaxy platform designed to make analysis of multiple genome alignments truly accessible for biologists. These tools are available through both a web-based graphical user interface and a command-line interface. Availability and Implementation: This open-source toolset was implemented in Python and has been integrated into the online data analysis platform Galaxy (public web access: http://usegalaxy.org; download: http://getgalaxy.org). Additional help is available as a live supplement from http://usegalaxy.org/u/dan/p/maf. Contact: james.taylor@emory.edu; anton@bx.psu.edu Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2011-09-01 2011-07-19 /pmc/articles/PMC3157923/ /pubmed/21775304 http://dx.doi.org/10.1093/bioinformatics/btr398 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Note Blankenberg, Daniel Taylor, James Nekrutenko, Anton Making whole genome multiple alignments usable for biologists |
title | Making whole genome multiple alignments usable for biologists |
title_full | Making whole genome multiple alignments usable for biologists |
title_fullStr | Making whole genome multiple alignments usable for biologists |
title_full_unstemmed | Making whole genome multiple alignments usable for biologists |
title_short | Making whole genome multiple alignments usable for biologists |
title_sort | making whole genome multiple alignments usable for biologists |
topic | Applications Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157923/ https://www.ncbi.nlm.nih.gov/pubmed/21775304 http://dx.doi.org/10.1093/bioinformatics/btr398 |
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