Association studies using genome scans to identify quantitative trait loci for multifactorial disorders, with anything approaching reasonable power, have been compromised by the need for a very dense array of genetic markers and large numbers of affected individuals. These requirements impose enormous burdens on the genotyping capacity for most laboratories. DNA pooling has been proposed as a possible approach to reduce genotyping costs and effort. We report on the application of the SNaPIT™ technology to evaluate allele frequencies in pooled DNA samples and conclude that it offers a cost effective, efficient and accurate estimator and provides several advantages over competing technologies in this regard.link_to_subscribed_fulltex
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
To undertake partial, or complete, genome screens by association-based methodology for quantitative ...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
Abstract Background Sustainable DNA resources and reliable high-throughput genotyping methods are re...
DNA pooling is a practical way to reduce the cost of large-scale association studies to identify sus...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
To undertake partial, or complete, genome screens by association-based methodology for quantitative ...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
Detecting alleles that confer small increments in susceptibility to disease will require large-scale...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
Abstract Background Sustainable DNA resources and reliable high-throughput genotyping methods are re...
DNA pooling is a practical way to reduce the cost of large-scale association studies to identify sus...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjec...