This item is licensed Korea Open Government License
dc.contributor.author
박정훈
dc.contributor.author
박현규
dc.contributor.author
신인경
dc.contributor.author
장효원
dc.contributor.author
정예림
dc.contributor.author
정윤경
dc.contributor.author
조대연
dc.date.accessioned
2019-08-28T07:42:12Z
dc.date.available
2019-08-28T07:42:12Z
dc.date.issued
2017-05-15
dc.identifier.issn
0956-5663
dc.identifier.uri
https://repository.kisti.re.kr/handle/10580/14716
dc.description.abstract
We herein describe a new mass spectrometry-based method for multiplex SNP genotyping by utilizing allelespecific ligation and strand displacement amplification (SDA) reaction. In this method, allele-specific ligation is first performed to discriminate base sequence variations at the SNP site within the PCR-amplified target DNA. The primary ligation probe is extended by a universal primer annealing site while the secondary
dc.language
eng
dc.relation.ispartofseries
Biosensors and Bioelectronics
dc.title
A mass spectrometry-based multiplex SNP genotyping by utilizing allelespecific ligation and strand displacement amplification