DELLY: structural variant discovery by integrated paired-end and split-read analysis

Motivation: The discovery of genomic structural variants (SVs) at high sensitivity and specificity is an essential requirement for characterizing naturally occurring variation and for understanding pathological somatic rearrangements in personal genome sequencing data. Of particular interest are int...

Descripción completa

Detalles Bibliográficos
Autores principales: Rausch, Tobias, Zichner, Thomas, Schlattl, Andreas, Stütz, Adrian M., Benes, Vladimir, Korbel, Jan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436805/
https://www.ncbi.nlm.nih.gov/pubmed/22962449
http://dx.doi.org/10.1093/bioinformatics/bts378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436805/
https://www.ncbi.nlm.nih.gov/pubmed/22962449
http://dx.doi.org/10.1093/bioinformatics/bts378

Ejemplares similares