An accurate method for quantifying and analyzing copy number variation in porcine KIT by an oligonucleotide ligation assay

BACKGROUND: Aside from single nucleotide polymorphisms, copy number variations (CNVs) are the most important factors in susceptibility to genetic disorders because they affect expression levels of genes. In previous studies, pyrosequencing, mini-sequencing, real-time PCR, invader assays and other te...

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Detalles Bibliográficos
Autores principales: Seo, Bo-Young, Park, Eung-Woo, Ahn, Sung-Jin, Lee, Sang-Ho, Kim, Jae-Hwan, Im, Hyun-Tae, Lee, Jun-Heon, Cho, In-Cheol, Kong, Il-Keun, Jeon, Jin-Tae
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228321/
https://www.ncbi.nlm.nih.gov/pubmed/18036219
http://dx.doi.org/10.1186/1471-2156-8-81

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228321/
https://www.ncbi.nlm.nih.gov/pubmed/18036219
http://dx.doi.org/10.1186/1471-2156-8-81

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