The TaqMan method for SNP genotyping.
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Summary
The detailed procedures for TaqMan SNP genotyping assay are described, including preparation of high-quality DNA samples, the operating protocol, clarification of technical issues, and discussion of several cautionary notes.
- Type
- article
- Published
- 2009-01-01
- Cited by
- 131
- References
- 42
- OpenAlex
- https://openalex.org/W204846666
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:28587282
Keywords
SNP genotyping, Genotyping, Single-nucleotide polymorphism, Molecular Inversion Probe, TaqMan
References
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- Genetics of metabolic syndrome
- SNP and mutation analysis.
- Genotyping Using the TaqMan Assay
- High-throughput genotyping.
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- High-throughput genotyping with single nucleotide polymorphisms.
- Single nucleotide polymorphism detection: allelic discrimination using TaqMan.
- The essence of SNPs.
- Primer: SNP-associated studies and what they can teach us
- Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
- A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers
- Progress in unraveling the genetics of coronary artery disease and myocardial infarction
- Progress in high throughput SNP genotyping methods
- Allelic discrimination using fluorogenic probes and the 5' nuclease assay.
- Four SNPS on Chromosome 9p21 Confer Risk to Premature, Familial CAD and MI in an American Caucasian Population (GeneQuest)
- Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.
- Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels
- Molecular genetics of coronary artery disease
- SNP discovery in associating genetic variation with human disease phenotypes.
Cited by
- Profiling of Childhood Adversity-Associated DNA Methylation Changes in Alcoholic Patients and Healthy Controls
- Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort
- Molecular Diversity and Population Structure at the CYP3A5 gene in Africa
- Myeloperoxidase is associated with cognitive function, brain morphology and subjective well-being in a cohort of elderly marathon runners
- Genotyping - by - Sequencing of sweet - stem and grain sorghum for linkage mapping
- High-throughput and functional SNP detection assays for oleic and linolenic acids in soybean
- The role of APOBEC3G in acute and early HIV-1 subtype C infection.
- High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR.
- Multi-allelic haplotype association identifies novel information different from single-SNP analysis: A new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI
- A Novel Molecular Diagnostic Marker for Familial and Early-Onset CAD and MI in the LRP8 Gene
- High-Throughput Carrier Screening Using TaqMan Allelic Discrimination
- Association between TNF-α-308 G/A gene polymorphism and gastric cancer risk: a systematic review and meta-analysis.
- Association of the CCR5Δ32 polymorphism and its ligand RANTES-403G/A polymorphism with coronary artery disease: a meta-analysis.
- Chaotic particle swarm optimization for detecting SNP–SNP interactions for CXCL12-related genes in breast cancer prevention
- Antiretroviral treatment-induced dyslipidemia in HIV-infected patients is influenced by the APOC3-related rs10892151 polymorphism
- Characterization of PTPN2 and its use as a biomarker.
- Computational and Experimental Approaches to Reveal the Effects of Single Nucleotide Polymorphisms with Respect to Disease Diagnostics
- Association study between GNB1L and three major mental disorders in Chinese Han populations.
- Genotyping on ALDH2: Comparison of Four Different Technologies
- Development of ARMS-PCR assay for genotyping of Pro12Ala SNP of PPARG gene: a cost effective way for case–control studies of type 2 diabetes in developing countries
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