Making whole genome multiple alignments usable for biologists.
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 21775304.
- Also identified by DOI 10.1093/bioinformatics/btr398 and PMC identifier 3157923.
- Licence recorded as CC BY-NC.
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Abstract
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. 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. james.taylor@emory.edu; anton@bx.psu.edu Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genomics
- Sequence Alignment
- Sequence Analysis, DNA
- Software