Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCR

For a wide range of diseases, SNPs in the genome are the underlying mechanism of dysfunction. Therefore, targeted detection of these variations is of high importance for early diagnosis and (familial) screenings. While allele-specific PCR has been around for many years, its adoption for SNP genotypi...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Lefever, Steve, Rihani, Ali, Van der Meulen, Joni, Pattyn, Filip, Van Maerken, Tom, Van Dorpe, Jo, Hellemans, Jan, Vandesompele, Jo
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6377641/
https://ncbi.nlm.nih.gov/pubmed/30770838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-38581-z
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