Fast and sensitive multiple alignment of large genomic sequences

BACKGROUND: Genomic sequence alignment is a powerful method for genome analysis and annotation, as alignments are routinely used to identify functional sites such as genes or regulatory elements. With a growing number of partially or completely sequenced genomes, multiple alignment is playing an inc...

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Vydáno v:	BMC Bioinformatics
Hlavní autoři:	Brudno, Michael, Chapman, Michael, Göttgens, Berthold, Batzoglou, Serafim, Morgenstern, Burkhard
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2003
Témata:	Methodology Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC521198/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14693042/ https://ncbi.nlm.nih.govhttps://doi.org/10.1186/1471-2105-4-66
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