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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Detalles Bibliográficos
Autores principales: Brudno, Michael, Chapman, Michael, Göttgens, Berthold, Batzoglou, Serafim, Morgenstern, Burkhard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC521198/
https://www.ncbi.nlm.nih.gov/pubmed/14693042
http://dx.doi.org/10.1186/1471-2105-4-66

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC521198/
https://www.ncbi.nlm.nih.gov/pubmed/14693042
http://dx.doi.org/10.1186/1471-2105-4-66

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