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A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing

Defining the architecture of a specific cancer genome, including its structural variants, is essential for understanding tumor biology, mechanisms of oncogenesis, and for designing effective personalized therapies. Short read paired-end sequencing is currently the most sensitive method for detecting...

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Detalles Bibliográficos
Autores principales:	Mijušković, Martina, Brown, Stuart M., Tang, Zuojian, Lindsay, Cory R., Efstathiadis, Efstratios, Deriano, Ludovic, Roth, David B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483208/ https://www.ncbi.nlm.nih.gov/pubmed/23144753 http://dx.doi.org/10.1371/journal.pone.0048314

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