SV-Bay: structural variant detection in cancer genomes using a Bayesian approach with correction for GC-content and read mappability

Motivation: Whole genome sequencing of paired-end reads can be applied to characterize the landscape of large somatic rearrangements of cancer genomes. Several methods for detecting structural variants with whole genome sequencing data have been developed. So far, none of these methods has combined...

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Detalles Bibliográficos
Autores principales: Iakovishina, Daria, Janoueix-Lerosey, Isabelle, Barillot, Emmanuel, Regnier, Mireille, Boeva, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Recomb-Seq/Recomb-Cbb
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896370/
https://www.ncbi.nlm.nih.gov/pubmed/26740523
http://dx.doi.org/10.1093/bioinformatics/btv751

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896370/
https://www.ncbi.nlm.nih.gov/pubmed/26740523
http://dx.doi.org/10.1093/bioinformatics/btv751

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