Cargando…
Reconstructing cancer genomes from paired-end sequencing data
BACKGROUND: A cancer genome is derived from the germline genome through a series of somatic mutations. Somatic structural variants - including duplications, deletions, inversions, translocations, and other rearrangements - result in a cancer genome that is a scrambling of intervals, or "blocks&...
Autores principales: | Oesper, Layla, Ritz, Anna, Aerni, Sarah J, Drebin, Ryan, Raphael, Benjamin J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358655/ https://www.ncbi.nlm.nih.gov/pubmed/22537039 http://dx.doi.org/10.1186/1471-2105-13-S6-S10 |
Ejemplares similares
-
Reconstruction of clonal trees and tumor composition from multi-sample sequencing data
por: El-Kebir, Mohammed, et al.
Publicado: (2015) -
THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data
por: Oesper, Layla, et al.
Publicado: (2013) -
PEAT: an intelligent and efficient paired-end sequencing adapter trimming algorithm
por: Li, Yun-Lung, et al.
Publicado: (2015) -
Reconstructing genome mixtures from partial adjacencies
por: Mahmoody, Ahmad, et al.
Publicado: (2012) -
Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine
por: Raphael, Benjamin J, et al.
Publicado: (2014)