底漆延伸
基因分型
SNP基因分型
分子反转探针
底漆(化妆品)
SNP公司
生物
单核苷酸多态性
基因座(遗传学)
寡核苷酸
遗传学
基因型
计算生物学
分子生物学
DNA
化学
基因
基序列
有机化学
作者
Stacey Gabriel,Liuda Ziaugra
标识
DOI:10.1002/0471142905.hg0212s42
摘要
Abstract Many high‐throughput single‐nucleotide polymorphism (SNP) genotyping technologies are currently available. The method for SNP genotyping described in this unit is based on the commercially available Sequenom MassARRAY platform which offers several attractive features for users desiring an accurate SNP genotyping assay. The assay described is based on primer extension and offers two levels of specificity. First a locus‐specific PCR reaction takes place, followed by a locus‐specific primer extension reaction (homogeneous Mass Extend, or hME assay) in which an oligonucleotide primer anneals immediately upstream of the polymorphic site being genotyped. The extension of the primer is according to the sequence of the variant site and can be a single complementary base or a series of complementary bases. Through the use of MALDI‐TOF mass spectrometry, the mass of the extended primer is determined. The preparation of probe and genomic DNA is also described in this unit.
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