Detection of genotyping errors by Hardy-Weinberg equilibrium testing

被引:300
作者
Hosking, L
Lumsden, S
Lewis, K
Yeo, A
McCarthy, L
Bansal, A
Riley, J
Purvis, I
Xu, CF
机构
[1] GlaxoSmithKline Med Res Ctr, Stevenage SG1 2NY, Herts, England
[2] GlaxoSmithKline Med Res Ctr, Harlow CM19 5AW, Essex, England
关键词
Hardy-Weinberg equilibrium; genotyping; error;
D O I
10.1038/sj.ejhg.5201164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genotyping data sets may contain errors that, in some instances, lead to false conclusions. Deviation from Hardy - Weinberg equilibrium (HWE) in random samples may be indicative of problematic assays. This study has analysed 107 000 genotypes generated by TaqMan, RFLP, sequencing or mass spectrometric methods from 443 single-nucleotide polymorphisms ( SNPs). These SNPs are distributed both within genes and in intergenic regions. Genotype distributions for 36 out of 313 assays (11.5%) whose minor allele frequencies were 40.05 deviated from HWE (P<0.05). Some of the possible reasons for this deviation were explored: assays for five SNPs proved nonspecific, and genotyping errors were identified in 21 SNPs. For the remaining 10 SNPs, no reasons for deviation from HWE were identified. We demonstrate the successful identification of a proportion of nonspecific assays, and assays harbouring genotyping error. Consequently, our current high- throughput genotyping system incorporates tests for both assay specificity and deviation from HWE, to minimise the genotype error rate and therefore improve data quality.
引用
收藏
页码:395 / 399
页数:5
相关论文
共 36 条
[21]   Linkage analysis in the presence of errors IV:: Joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified [J].
Göring, HHH ;
Terwilliger, JD .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (04) :1310-1327
[22]   Linkage analysis in the presence of errors III:: Marker loci and their map as nuisance parameters [J].
Göring, HHH ;
Terwilliger, JD .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (04) :1298-1309
[23]   Mendelian proportions in a mixed population [J].
Hardy, GH .
SCIENCE, 1908, 28 :49-50
[24]   Molecular fossils in the human genome: Identification and analysis of the pseudogenes in chromosomes 21 and 22 [J].
Harrison, PM ;
Hegyi, H ;
Balasubramanian, S ;
Luscombe, NM ;
Bertone, P ;
Echols, N ;
Johnson, T ;
Gerstein, M .
GENOME RESEARCH, 2002, 12 (02) :272-280
[25]   Identification of a psoriasis susceptibility candidate gene by linkage disequilibrium mapping with a localized single nucleotide polymorphism map [J].
Hewett, D ;
Samuelsson, L ;
Polding, J ;
Enlund, F ;
Smart, D ;
Cantone, K ;
See, CG ;
Chadha, S ;
Inerot, A ;
Enerback, C ;
Montgomery, D ;
Christodolou, C ;
Robinson, P ;
Matthews, P ;
Plumpton, M ;
Dykes, C ;
Wahlstrom, J ;
Swanbeck, G ;
Martinsson, T ;
Roses, A ;
Riley, J ;
Purvis, I .
GENOMICS, 2002, 79 (03) :305-314
[26]   Linkage disequilibrium mapping identifies a 390 kb region associated with CYP2D6 poor drug metabolising activity [J].
Hosking L.K. ;
Boyd P.R. ;
Xu C.F. ;
Nissum M. ;
Cantone K. ;
Purvis I.J. ;
Khakhar R. ;
Barnes M.R. ;
Liberwirth U. ;
Hagen-Mann K. ;
Ehm M.G. ;
Riley J.H. .
The Pharmacogenomics Journal, 2002, 2 (3) :165-175
[27]   Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine [J].
McCarthy, LC ;
Hosford, DA ;
Riley, JH ;
Bird, MI ;
White, NJ ;
Hewett, DR ;
Peroutka, SJ ;
Griffiths, LR ;
Boyd, PR ;
Lea, RA ;
Bhatti, SM ;
Hosking, LK ;
Hood, CM ;
Jones, KW ;
Handley, AR ;
Rallan, R ;
Lewis, KF ;
Yeo, AJM ;
Williams, PM ;
Priest, RC ;
Khan, P ;
Donnelly, C ;
Lumsden, SM ;
O'Sullivan, J ;
See, CG ;
Smart, DH ;
Shaw-Hawkins, S ;
Patel, J ;
Langrish, TC ;
Feniuk, W ;
Knowles, RG ;
Thomas, M ;
Libri, V ;
Montgomery, DS ;
Manasco, PK ;
Xu, CF ;
Dykes, C ;
Humphrey, PPA ;
Roses, AD ;
Purvis, IJ .
GENOMICS, 2001, 78 (03) :135-149
[28]   Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test [J].
Mitchell, AA ;
Cutler, DJ ;
Chakravarti, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (03) :598-610
[29]  
MOTE VL, 1965, BIOMETRIKA, V52, P95, DOI 10.1093/biomet/52.1-2.95
[30]  
O'Connell JR, 2002, BIOSTATISTICAL GENET, P348