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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...
Autor principal: | Wittler, Roland |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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 |
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