Cargando…
Partitioning of copy-number genotypes in pedigrees
BACKGROUND: Copy number variations (CNVs) and polymorphisms (CNPs) have only recently gained the genetic community's attention. Conservative estimates have shown that CNVs and CNPs might affect more than 10% of the genome and that they may be at least as important as single nucleotide polymorph...
Autores principales: | Perreault, Louis-Philippe Lemieux, Andelfinger, Gregor U, Asselin, Géraldine, Dubé, Marie-Pierre |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874807/ https://www.ncbi.nlm.nih.gov/pubmed/20438641 http://dx.doi.org/10.1186/1471-2105-11-226 |
Ejemplares similares
-
genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools
por: Lemieux Perreault, Louis-Philippe, et al.
Publicado: (2016) -
SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels
por: Sanders, Mathijs A, et al.
Publicado: (2008) -
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments
por: Magi, Alberto, et al.
Publicado: (2017) -
dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsets
por: Baron, Robert V, et al.
Publicado: (2015) -
Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease
por: Hitz, Marc-Phillip, et al.
Publicado: (2012)