Genotyping pooled DNA on microarrays: A systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits

被引:83
作者
Butcher, LM
Meaburn, E
Liu, L
Fernandes, C
Hill, L
Al-Chalabi, A
Plomin, R
Schalkwyk, L
Craig, IW
机构
[1] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London SE5 8AF, England
[2] Inst Psychiat, Dept Neurol, Neurogenet Sect, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
association; DNA pooling; high-throughput genotyping; microarrays; quantitative trait loci (QTLs); single nucleotide polymorphisms (SNPs);
D O I
10.1023/B:BEGE.0000038493.26202.d3
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
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(R) Mapping 10K Array Xba 131). The average correlation was 0.973 between the allele frequency estimates for the three microarrays using the same DNA pool. The correlation was 0.923 between the average of the three microarray estimates using pooled DNA and individual genotyping estimates for a Caucasian population as provided by Affymetrix (NetAff(x)(TM)). Thus, genotyping pooled DNA on microarrays can provide a systematic and powerful approach for identifying QTL associations for complex traits including behavioral dimensions and disorders.
引用
收藏
页码:549 / 555
页数:7
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