PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data

Next-generation sequencing technologies expedited research to develop efficient computational tools for the identification of structural variants (SVs) and their use to study human diseases. As deeper data is obtained, the existence of higher complexity SVs in some genomes becomes more evident, but...

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Detalles Bibliográficos
Autores principales: Escaramís, Geòrgia, Tornador, Cristian, Bassaganyas, Laia, Rabionet, Raquel, Tubio, Jose M. C., Martínez-Fundichely, Alexander, Cáceres, Mario, Gut, Marta, Ossowski, Stephan, Estivill, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660373/
https://www.ncbi.nlm.nih.gov/pubmed/23704902
http://dx.doi.org/10.1371/journal.pone.0063377

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660373/
https://www.ncbi.nlm.nih.gov/pubmed/23704902
http://dx.doi.org/10.1371/journal.pone.0063377

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