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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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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Principais autores: Brudno, Michael, Chapman, Michael, Göttgens, Berthold, Batzoglou, Serafim, Morgenstern, Burkhard
Formato: Artigo
Idioma:Inglês
Publicado em: BMC 2003
Assuntos:
Acesso em linha: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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