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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Dades bibliogràfiques

Publicat a:	BMC Bioinformatics
Autors principals:	Brudno, Michael, Chapman, Michael, Göttgens, Berthold, Batzoglou, Serafim, Morgenstern, Burkhard
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2003
Matèries:	Methodology Article
Accés en línia:	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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