Difference between revisions of "GenomeMapper"
m (Text replace - "([= ])[Mm]apping," to "$1Read mapping,") |
m (Text replace - "Alignment" to "Sequence alignment") |
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{{Bioinformatics application | {{Bioinformatics application | ||
|sw summary=GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference. | |sw summary=GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference. | ||
| − | |bio method= | + | |bio method=Sequence alignment, Read mapping, |
|created at=Max Planck Institute, | |created at=Max Planck Institute, | ||
}} | }} | ||
Latest revision as of 16:04, 19 December 2015
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Application data |
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| Principal bioinformatics method(s) | Sequence alignment, Read mapping |
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| Created at | Max Planck Institute |
| Maintained? | Maybe |
Summary: GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference.
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See Shore reference for more information.
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