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DB(2): a probabilistic approach for accurate detection of tandem duplication breakpoints using paired-end reads

BACKGROUND: With the advent of paired-end high throughput sequencing, it is now possible to identify various types of structural variation on a genome-wide scale. Although many methods have been proposed for structural variation detection, most do not provide precise boundaries for identified varian...

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Detalles Bibliográficos
Publicado en:BMC Genomics
Autores principales: Yavaş, Gökhan, Koyutürk, Mehmet, Gould, Meetha P, McMahon, Sarah, LaFramboise, Thomas
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2014
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4234483/
https://ncbi.nlm.nih.gov/pubmed/24597945
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-175
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