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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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Autors principals: Brudno, Michael, Chapman, Michael, Göttgens, Berthold, Batzoglou, Serafim, Morgenstern, Burkhard
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2003
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC521198/
https://ncbi.nlm.nih.gov/pubmed/14693042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-4-66
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