Allelic association studies provide the most powerful method for locating genes of small effect contributing to complex diseases and traits. However, in outbred populations, allelic association is usually maintained only over distances of <=1 cM. Therefore, systematic searches over large regions are costly. Here we present a method involving DNA pooling that can be used as a rapid preliminary screen for allelic association with the most common class of polymorphic markers, single-sequence repeats. Patient and control samples are pooled separately, and markers are typed in the two pools. By use of primers with fluorescent 5' ends, PCR products can be analyzed on an automated sequencing apparatus. Allele image patterns (AIPs) produced for the...
Pooled DNA samples have been used in association studies of Mendelian disease genes. This method inv...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
Allelic association studies provide the most powerful method for locating genes of small effect cont...
SummaryAllelic association studies provide the most powerful method for locating genes of small effe...
Abstract Background Pooling genomic DNA samples within clinical classes of disease followed by genot...
Association studies using DNA pools are in principle powerful and efficient to detect association be...
To undertake partial, or complete, genome screens by association-based methodology for quantitative ...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
SummaryGenomic screening to map disease loci by association requires automation, pooling of DNA samp...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
We have evaluated a pooling approach that can reduce the number of polymerase chain reactions in a s...
Abstract Background DNA pooling is a technique to reduce genotyping effort while incurring only mino...
Pooled DNA samples have been used in association studies of Mendelian disease genes. This method inv...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
Allelic association studies provide the most powerful method for locating genes of small effect cont...
SummaryAllelic association studies provide the most powerful method for locating genes of small effe...
Abstract Background Pooling genomic DNA samples within clinical classes of disease followed by genot...
Association studies using DNA pools are in principle powerful and efficient to detect association be...
To undertake partial, or complete, genome screens by association-based methodology for quantitative ...
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex trai...
SummaryGenomic screening to map disease loci by association requires automation, pooling of DNA samp...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative t...
We have evaluated a pooling approach that can reduce the number of polymerase chain reactions in a s...
Abstract Background DNA pooling is a technique to reduce genotyping effort while incurring only mino...
Pooled DNA samples have been used in association studies of Mendelian disease genes. This method inv...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...