Results 291 to 300 of about 120,949 (314)
Some of the next articles are maybe not open access.

SNP Genotyping: The KASP Assay

2014
The KASP genotyping assay utilizes a unique form of competitive allele-specific PCR combined with a novel, homogeneous, fluorescence-based reporting system for the identification and measurement of genetic variation occurring at the nucleotide level to detect single nucleotide polymorphisms (SNPs) or inserts and deletions (InDels).
John Holme, Jeffrey Anthony, Chunlin He
openaire   +2 more sources

SNP marker detection and genotyping in tilapia

Molecular Ecology Resources, 2012
AbstractWe have generated a unique resource consisting of nearly 175 000 short contig sequences and 3569 SNP markers from the widely cultured GIFT (Genetically Improved Farmed Tilapia) strain of Nile tilapia (Oreochromis niloticus). In total, 384 SNPs were selected to monitor the wider applicability of the SNPs by genotyping tilapia individuals from ...
van Bers, N.E.M.   +4 more
openaire   +4 more sources

The TaqMan Method for SNP Genotyping

2009
Single nucleotide polymorphisms (SNPs) are common DNA sequence variations that occur at single bases within the genome. SNPs have been instrumental in elucidating the genetic basis of common, complex diseases using genome-wide association studies, candidate gene case-control association studies, and genome-wide linkage analyses.
Gong Qing Shen   +3 more
openaire   +3 more sources

Assessment of two flexible and compatible SNP genotyping platforms: TaqMan® SNP Genotyping Assays and the SNPlex™ Genotyping System

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 2005
In this review we describe the principles, protocols, and applications of two commercially available SNP genotyping platforms, the TaqMan SNP Genotyping Assays and the SNPlex Genotyping System. Combined, these two technologies meet the requirements of multiple SNP applications in genetics research and pharmacogenetics.
Michael D. Rhodes   +3 more
openaire   +3 more sources

SNP genotype calling with MapReduce [PDF]

open access: possibleProceedings of third international workshop on MapReduce and its Applications Date, 2012
Genotype measurement is a key step in genome-wide association studies -- those studies that aim to uncover the underlying genetic causes of physical traits, including disease. The leading technology for measuring genotypes is the SNP microarray, where hundreds of thousands of genetic variants are interrogated simultaneously.
Gianluigi Zanetti   +2 more
openaire   +1 more source

SNP Discovery and Genotyping

2007
The identification of genes affecting complex traits (i.e., biological traits affected by several genetic and environmental factors) is a very difficult and challenging task (1, 2, 3). For many complex traits, the observable variation between individuals is quantitative; hence, loci affecting such traits are generally termed quantitative trait loci ...
Jun Wang   +3 more
openaire   +2 more sources

Allele-Specific PCR in SNP Genotyping

2009
The increasing need for large-scale genotyping applications of single nucleotide polymorphisms (SNPs) in model and nonmodel organisms requires the development of low-cost technologies accessible to minimally equipped laboratories. The method presented here allows efficient discrimination of SNPs by allele-specific PCR in a single reaction with standard
Gaudet Muriel   +3 more
openaire   +3 more sources

Isothermal Amplification Methods for the SNP Genotyping

Current Molecular Medicine, 2019
The demands for genotyping techniques with acceptable precision, accuracy, cost-effectiveness in high throughput formats made driving forces for continuous development of novel technologies. A wide range of mutation detection techniques based on polymerase chain reaction (PCR) have been introduced.
Fatemeh Heidari Sharafdarkolaee   +3 more
openaire   +2 more sources

SNP Genotyping: Technologies and Biomedical Applications

Annual Review of Biomedical Engineering, 2007
Single nucleotide polymorphisms (SNPs) are the most frequently occurring genetic variation in the human genome, with the total number of SNPs reported in public SNP databases currently exceeding 9 million. SNPs are important markers in many studies that link sequence variations to phenotypic changes; such studies are expected to advance the ...
Sobin Kim, Ashish Misra
openaire   +2 more sources

A comprehensive evaluation of SNP genotype imputation

Human Genetics, 2008
Genome-wide association studies have contributed significantly to the genetic dissection of complex diseases. In order to increase the power of existing marker sets even further, methods have been proposed to predict individual genotypes at un-typed loci from other marker sets by imputation, usually employing HapMap data as a reference.
David Ellinghaus   +4 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy