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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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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2228321/ https://ncbi.nlm.nih.gov/pubmed/18036219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-8-81 |
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