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High-Throughput SNP Genotyping

Whole genome approaches using single nucleotide polymorphism (SNP) markers have the potential to transform complex disease genetics and expedite pharmacogenetics research. This has led to a requirement for high-throughput SNP genotyping platforms. Development of a successful high-throughput genotypi...

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Detalles Bibliográficos
Autores principales: Jenkins, Suzanne, Gibson, Neil
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447245/
https://www.ncbi.nlm.nih.gov/pubmed/18628885
http://dx.doi.org/10.1002/cfg.130
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author Jenkins, Suzanne
Gibson, Neil
author_facet Jenkins, Suzanne
Gibson, Neil
author_sort Jenkins, Suzanne
collection PubMed
description Whole genome approaches using single nucleotide polymorphism (SNP) markers have the potential to transform complex disease genetics and expedite pharmacogenetics research. This has led to a requirement for high-throughput SNP genotyping platforms. Development of a successful high-throughput genotyping platform depends on coupling reliable assay chemistry with an appropriate detection system to maximise efficiency with respect to accuracy, speed and cost. Current technology platforms are able to deliver throughputs in excess of 100 000 genotypes per day, with an accuracy of >99%, at a cost of 20–30 cents per genotype. In order to meet the demands of the coming years, however, genotyping platforms need to deliver throughputs in the order of one million genotypes per day at a cost of only a few cents per genotype. In addition, DNA template requirements must be minimised such that hundreds of thousands of SNPs can be interrogated using a relatively small amount of genomic DNA. As such, it is predicted that the next generation of high-throughput genotyping platforms will exploit large-scale multiplex reactions and solid phase assay detection systems.
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spelling pubmed-24472452008-07-14 High-Throughput SNP Genotyping Jenkins, Suzanne Gibson, Neil Comp Funct Genomics Research Article Whole genome approaches using single nucleotide polymorphism (SNP) markers have the potential to transform complex disease genetics and expedite pharmacogenetics research. This has led to a requirement for high-throughput SNP genotyping platforms. Development of a successful high-throughput genotyping platform depends on coupling reliable assay chemistry with an appropriate detection system to maximise efficiency with respect to accuracy, speed and cost. Current technology platforms are able to deliver throughputs in excess of 100 000 genotypes per day, with an accuracy of >99%, at a cost of 20–30 cents per genotype. In order to meet the demands of the coming years, however, genotyping platforms need to deliver throughputs in the order of one million genotypes per day at a cost of only a few cents per genotype. In addition, DNA template requirements must be minimised such that hundreds of thousands of SNPs can be interrogated using a relatively small amount of genomic DNA. As such, it is predicted that the next generation of high-throughput genotyping platforms will exploit large-scale multiplex reactions and solid phase assay detection systems. Hindawi Publishing Corporation 2002-02 /pmc/articles/PMC2447245/ /pubmed/18628885 http://dx.doi.org/10.1002/cfg.130 Text en Copyright © 2002 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jenkins, Suzanne
Gibson, Neil
High-Throughput SNP Genotyping
title High-Throughput SNP Genotyping
title_full High-Throughput SNP Genotyping
title_fullStr High-Throughput SNP Genotyping
title_full_unstemmed High-Throughput SNP Genotyping
title_short High-Throughput SNP Genotyping
title_sort high-throughput snp genotyping
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447245/
https://www.ncbi.nlm.nih.gov/pubmed/18628885
http://dx.doi.org/10.1002/cfg.130
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