Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data

Copy number variations (CNVs) are gains and losses of genomic sequence between two individuals of a species when compared to a reference genome. The data from single nucleotide polymorphism (SNP) microarrays are now routinely used for genotyping, but they also can be utilized for copy number detecti...

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Detalles Bibliográficos
Autores principales: Xu, Lingyang, Hou, Yali, Bickhart, Derek M., Song, Jiuzhou, Liu, George E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003459/
https://www.ncbi.nlm.nih.gov/pubmed/27605188
http://dx.doi.org/10.3390/microarrays2030171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003459/
https://www.ncbi.nlm.nih.gov/pubmed/27605188
http://dx.doi.org/10.3390/microarrays2030171

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