Large samples and systematic screens of thousands of DNA markers are needed to detect quantitative trait loci (QTLs) of small effect size. One approach to conduct systematic genome scans for association is to use microarrays which, although expensive and non-reusable, simultaneously genotype thousands of single-nucleotide polymorphisms (SNPs). This brief report provides proof of principle that groups of pooled DNA (for example cases and controls) can be genotyped reliably on a microarray. DNA was pooled for 105 Caucasian males and genotyped three times on microarrays for more than 10,000 SNPs (Affymetrix GeneChip® Mapping 10K Array Xba 131). The average correlation was 0.973 between the allele frequency estimates for the three microarrays u...
Abstract Background Genotyping technology has advanced such that genome-wide association studies of ...
Abstract Background We report an attempt to extend the previously successful approach of combining S...
Abstract Background Pooling genomic DNA samples within clinical classes of disease followed by genot...
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...
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...
Background: Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
Background Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Background Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Background: Genetic influences underpinning complex traits are thought to involve multiple quantitat...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Abstract Background Genotyping technology has advanced such that genome-wide association studies of ...
Abstract Background We report an attempt to extend the previously successful approach of combining S...
Abstract Background Pooling genomic DNA samples within clinical classes of disease followed by genot...
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...
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...
Background: Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Pooling genomic DNA samples within clinical classes of disease for use in whole-genome single nucleo...
Background Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Background Quantitative trait locus (QTL) theory predicts that genetic influence on complex traits ...
Background: Genetic influences underpinning complex traits are thought to involve multiple quantitat...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Evidence is mounting that multiple genes are involved in complex traits and that these each account ...
Abstract Background Genotyping technology has advanced such that genome-wide association studies of ...
Abstract Background We report an attempt to extend the previously successful approach of combining S...
Abstract Background Pooling genomic DNA samples within clinical classes of disease followed by genot...