Detection and integration of genotyping errors in statistical genetics

被引:279
作者
Sobel, E [1 ]
Papp, JC
Lange, K
机构
[1] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Biomath, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Dept Stat, Los Angeles, CA USA
基金
美国国家卫生研究院;
关键词
D O I
10.1086/338920
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Detection of genotyping errors and integration of such errors in statistical analysis are relatively neglected topics, given their importance in gene mapping. A few inopportunely placed errors, if ignored, can tremendously affect evidence for linkage. The present study takes a fresh look at the calculation of pedigree likelihoods in the presence of genotyping error. To accommodate genotyping error, we present extensions to the Lander-Green-Kruglyak deterministic algorithm for small pedigrees and to the Markov-chain Monte Carlo stochastic algorithm for large pedigrees. These extensions can accommodate a variety of error models and refrain from simplifying assumptions, such as allowing, at most, one error per pedigree. In principle, almost any statistical genetic analysis can be performed taking errors into account, without actually correcting or deleting suspect genotypes. Three examples illustrate the possibilities. These examples make use of the full pedigree data, multiple linked markers, and a prior error model. The first example is the estimation of genotyping error rates from pedigree data. The second-and currently most useful-example is the computation of posterior mistyping probabilities. These probabilities cover both Mendelian-consistent and Mendelian-inconsistent errors. The third example is the selection of the true pedigree structure connecting a group of people from among several competing pedigree structures. Paternity testing and twin zygosity testing are typical applications.
引用
收藏
页码:496 / 508
页数:13
相关论文
共 63 条
[1]   The impact of genotyping error on family-based analysis of quantitative traits [J].
Abecasis, GR ;
Cherny, SS ;
Cardon, LR .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (02) :130-134
[2]   The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures [J].
Akey, JM ;
Zhang, K ;
Xiong, MM ;
Doris, P ;
Jin, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) :1447-1456
[3]  
[Anonymous], AM J HUMAN GENETICS, DOI DOI 10.1038/srep40577
[4]   Accurate inference of relationships in sib-pair linkage studies [J].
Boehnke, M ;
Cox, NJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :423-429
[5]   Estimation of pairwise relationships in the presence of genotyping errors [J].
Broman, KW ;
Weber, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (05) :1563-1564
[6]  
BRZUSTOWICZ LM, 1993, AM J HUM GENET, V53, P1137
[7]  
BUETOW KH, 1991, AM J HUM GENET, V49, P985
[8]   QUANTITATIVE TRAIT LOCUS FOR READING-DISABILITY (VOL 266, PG 276, 1994) [J].
CARDON, LR ;
SMITH, SD ;
FULKER, DW ;
KIMBERLING, WJ ;
PENNINGTON, BF ;
DEFRIES, JC .
SCIENCE, 1995, 268 (5217) :1553-1553
[9]   QUANTITATIVE TRAIT LOCUS FOR READING-DISABILITY ON CHROMOSOME-6 [J].
CARDON, LR ;
SMITH, SD ;
FULKER, DW ;
KIMBERLING, WJ ;
PENNINGTON, BF ;
DEFRIES, JC .
SCIENCE, 1994, 266 (5183) :276-279
[10]  
CAVALLISFORZA LL, 1971, GENETICS HUMAN POPUL