Development of a rapid and reliable single-tube multiplex real-time PCR method for
is significantly associated with cutaneous adverse drug reactions caused by aromatic antiepileptic drugs. Here, we aimed to establish a fast and reliable detection method for genotyping. A single-tube multiplex quantitative real-time polymerase chain reaction (qPCR) assay for genotyping was establis...
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Published in | Pharmacogenomics Vol. 20; no. 11; pp. 803 - 812 |
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Format | Journal Article |
Language | English |
Published |
Future Medicine Ltd
01.08.2019
01.07.2019 01.06.2019 |
Subjects | |
Online Access | Get full text |
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Summary: | is significantly associated with cutaneous adverse drug reactions caused by aromatic antiepileptic drugs. Here, we aimed to establish a fast and reliable detection method for
genotyping.
A single-tube multiplex quantitative real-time polymerase chain reaction (qPCR) assay for
genotyping was established by combining allele-specific primers with TaqMan probes.
A 100% concordance was observed between qPCR and SBT result in 106 Han subjects. The detection limit of the new method was 0.05 ng DNA. The positive rate of
in Tibetans (55.6%, n = 81) was significantly higher than those in Han (34%, n = 106), Uighur (27.5%, n = 102), Bouyei (25.9%, n = 116) and Miao populations (26.5%, n = 113).
The newly established qPCR assay was reliable for
screening in clinical applications. |
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ISSN: | 1462-2416 1744-8042 |
DOI: | 10.2217/pgs-2019-0052 |