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SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis
Author(s) -
Stéphanie Le Hellard,
Stéphane J. Ballereau,
Peter M. Visscher,
Helen S. Torrance,
Jeni Pinson,
Stewart W. Morris,
Marian Thomson,
Colin A. Semple,
Walter Muir,
Douglas Blackwood,
David J. Porteous,
Kathryn L. Evans
Publication year - 2002
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gnf070
Subject(s) - genotyping , biology , repeatability , genetics , allele , allele frequency , snp genotyping , single nucleotide polymorphism , snp , robustness (evolution) , genotype , computational biology , statistics , gene , mathematics
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.

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