Cargando…
Quantification of read species behavior within whole genome sequencing of cancer genomes for the stratification and visualization of genomic variation
The cancer genome is abnormal genome, and the ability to monitor its sequence had undergone a technological revolution. Yet prognosis and diagnosis remain an expert-based decision, with only limited abilities to provide machine-based decisions. We introduce a heterogeneity-based method for stratifyi...
Autores principales: | Hibsh, Dror, Buetow, Kenneth H., Yaari, Gur, Efroni, Sol |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872078/ https://www.ncbi.nlm.nih.gov/pubmed/26809676 http://dx.doi.org/10.1093/nar/gkw031 |
Ejemplares similares
-
Identification of large-scale genomic variation in cancer genomes using in silico reference models
por: Killcoyne, Sarah, et al.
Publicado: (2016) -
RepARK—de novo creation of repeat libraries from whole-genome NGS reads
por: Koch, Philipp, et al.
Publicado: (2014) -
Long-read whole-genome methylation patterning using enzymatic base conversion and nanopore sequencing
por: Sakamoto, Yoshitaka, et al.
Publicado: (2021) -
Primase-based whole genome amplification
por: Li, Ying, et al.
Publicado: (2008) -
NOVOPlasty: de novo assembly of organelle genomes from whole genome data
por: Dierckxsens, Nicolas, et al.
Publicado: (2017)