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Unraveling overlapping deletions by agglomerative clustering

BACKGROUND: Structural variations in human genomes, such as deletions, play an important role in cancer development. Next-Generation Sequencing technologies have been central in providing ways to detect such variations. Methods like paired-end mapping allow to simultaneously analyze data from severa...

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Detalles Bibliográficos
Autor principal: Wittler, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549816/
https://www.ncbi.nlm.nih.gov/pubmed/23369161
http://dx.doi.org/10.1186/1471-2164-14-S1-S12