Cargando…
Detection and reconstruction of tandemly organized de novo copy number variations
BACKGROUND: The characterization of structural variations (SV) such as insertions, deletions and copy number variations is a critical step in the process of understanding the full genetic architecture of organisms. Copy number variations (CNV) have attracted much recent attention due to their effect...
Autores principales: | He, Dan, Furlotte, Nicholas, Eskin, Eleazar |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024866/ https://www.ncbi.nlm.nih.gov/pubmed/21172047 http://dx.doi.org/10.1186/1471-2105-11-S11-S12 |
Ejemplares similares
-
De novo copy number variations in cloned dogs from the same nuclear donor
por: Jung, Seung-Hyun, et al.
Publicado: (2013) -
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
por: Zarrei, Mehdi, et al.
Publicado: (2018) -
Neurodevelopmental disease genes implicated by de
novo mutation and copy number variation morbidity
por: Coe, Bradley P., et al.
Publicado: (2018) -
In vivo and in vitro ageing results in accumulation of de novo copy number variations in bulls
por: Revay, Tamas, et al.
Publicado: (2017) -
KOMB: K-core based de novo characterization of copy number variation in microbiomes
por: Balaji, Advait, et al.
Publicado: (2022)