SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucleotide polymorphisms on pooled DNAs. We conclude that (i) the frequencies of the two alleles in pools should be corrected with a factor for unequal allelic amplification, which should be estimated from the mean ratio of a set of heterozygotes (k); (ii) the repeatability of an assay is more important than pinpoint accuracy when estimating allele frequencies, and assays should therefore be optimised to increase the repeatability; and (iii) the size of a pool has a relatively small effect on the accuracy of allele frequency estimation. We therefore recommend that large pools are genotyped and replicated a minimum of four times. In addition, we describe statistical approaches to allow rigorous comparison of DNA pool results. Finally, we describe an extension to our ACeDB database that facilitates management and analysis of the data generated by association studies.

[1]  R. Quatrano Genomics , 1998, Plant Cell.

[2]  M. Owen,et al.  Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography , 1999, Human Genetics.

[3]  N. Risch Searching for genetic determinants in the new millennium , 2000, Nature.

[4]  D. Harold,et al.  Determining SNP allele frequencies in DNA pools. , 2000, BioTechniques.

[5]  S. Germer,et al.  High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR. , 2000, Genome research.

[6]  Michael Owen,et al.  Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools , 2000, Human Genetics.

[7]  M. Daly,et al.  A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.

[8]  M. Xiong,et al.  The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures. , 2001, American journal of human genetics.

[9]  D. Bentley,et al.  A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder. , 2001, Genomics.

[10]  A. Syvänen Accessing genetic variation: genotyping single nucleotide polymorphisms , 2001, Nature Reviews Genetics.

[11]  K. Okano,et al.  Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER). , 2001, Nucleic acids research.

[12]  L. Cardon,et al.  Association study designs for complex diseases , 2001, Nature Reviews Genetics.

[13]  T. Tahira,et al.  Precise estimation of allele frequencies of single-nucleotide polymorphisms by a quantitative SSCP analysis of pooled DNA. , 2001, American journal of human genetics.

[14]  Stacey S Cherny,et al.  The impact of genotyping error on family-based analysis of quantitative traits , 2001, European Journal of Human Genetics.

[15]  R. Strausberg,et al.  High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[16]  E. Boerwinkle,et al.  High‐throughput multiplex SNP genotyping with MALDI‐TOF mass spectrometry: Practice, problems and promise , 2001, Human mutation.

[17]  G. Kirov,et al.  Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools , 2002, Human Genetics.