BreaKmer: detection of structural variation in targeted massively parallel sequencing data using kmers

Genomic structural variation (SV), a common hallmark of cancer, has important predictive and therapeutic implications. However, accurately detecting SV using high-throughput sequencing data remains challenging, especially for ‘targeted’ resequencing efforts. This is critically important in the clini...

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Detalles Bibliográficos
Autores principales: Abo, Ryan P., Ducar, Matthew, Garcia, Elizabeth P., Thorner, Aaron R., Rojas-Rudilla, Vanesa, Lin, Ling, Sholl, Lynette M., Hahn, William C., Meyerson, Matthew, Lindeman, Neal I., Van Hummelen, Paul, MacConaill, Laura E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330340/
https://www.ncbi.nlm.nih.gov/pubmed/25428359
http://dx.doi.org/10.1093/nar/gku1211

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330340/
https://www.ncbi.nlm.nih.gov/pubmed/25428359
http://dx.doi.org/10.1093/nar/gku1211

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