Cargando…
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication
BACKGROUND: Intrachromosomal segmental duplications provide the substrate for non-allelic homologous recombination, facilitating extensive copy number variation in the human genome. Many multi-copy gene families are embedded within genomic regions with high levels of sequence identity (>95%) and...
Autores principales: | Cantsilieris, Stuart, Western, Patrick S, Baird, Paul N, White, Stefan J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035060/ https://www.ncbi.nlm.nih.gov/pubmed/24885186 http://dx.doi.org/10.1186/1471-2164-15-329 |
Ejemplares similares
-
CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data
por: Sinha, Rituparna, et al.
Publicado: (2015) -
Comprehensive Analysis of Copy Number Variation of Genes at Chromosome 1 and 10 Loci Associated with Late Age Related Macular Degeneration
por: Cantsilieris, Stuart, et al.
Publicado: (2012) -
The Role of Number of Copies, Structure, Behavior and Copy Number Variations (CNV) of the Y Chromosome in Male Infertility
por: Signore, Fabrizio, et al.
Publicado: (2019) -
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
por: Zhang, Li, et al.
Publicado: (2021) -
Copy Number Variation (CNV): A New Genomic Insight in Horses
por: Laseca, Nora, et al.
Publicado: (2022)