A survey of affected-sibship statistics for nonparametric linkage analysis.

We have compared the power of a large number of allele-sharing statistics for "nonparametric" linkage analysis with affected sibships. Our rationale was that there is an extensive literature comparing statistics for sibling pairs but that there has not been much guidance on how to choose statistics for studies that include sibships of various sizes. We concentrated on statistics that can be described as assigning scores to each identity-by-descent-sharing configuration that a pedigree might take on (Whittemore and Halpern 1994). We considered sibships of sizes two through five, 27 different genetic models, and varying recombination fractions between the marker and the trait locus. We tried to identify statistics whose power was robust over a wide variety of models. We found that the statistic that is probably used most often in such studies-S(all)-performs quite well, although it is not necessarily the best. We also found several other statistics (such as the R criterion, S(robdom), and the Sobel-and-Lange statistic C) that perform well in most situations, a few (such as S(-#geno) and the Feingold-and-Siegmund version of S(pairs)) that have high power only in very special situations, and a few (such as S(-#geno), the N criterion, and the Sobel-and-Lange statistic B) that seem to have low power for the majority of the trait models. For the most part, the same statistics performed well for all sibship sizes. We also used our results to give some suggestions regarding how to weight sibships of different sizes, in forming an overall statistic.

[1]  J. Green,et al.  Sibling Method for Detecting HLA-linked genes in disease. , 2008, Tissue antigens.

[2]  P. Holmans Likelihood‐ratio affected sib‐pair tests applied to multiply affected sibships: Issues of power and type I error rate , 2001, Genetic epidemiology.

[3]  P. Sham,et al.  Power comparison of parametric and nonparametric linkage tests in small pedigrees. , 2000, American journal of human genetics.

[4]  S E Hodge,et al.  Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases. , 1999, American journal of human genetics.

[5]  S. Bull,et al.  Down-weighting of multiple affected sib pairs leads to biased likelihood-ratio tests, under the assumption of no linkage. , 1999, American journal of human genetics.

[6]  A. Whittemore,et al.  Simple, robust linkage tests for affected sibs. , 1998, American journal of human genetics.

[7]  D. Weeks,et al.  Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation. , 1997, American journal of human genetics.

[8]  D. Siegmund,et al.  Strategies for mapping heterogeneous recessive traits by allele-sharing methods. , 1997, American journal of human genetics.

[9]  D. Siegmund,et al.  Combining information within and between pedigrees for mapping complex traits. , 1997, American journal of human genetics.

[10]  D. Curtis,et al.  Optimal weighting scheme for affected sib‐pair analysis of sibship data , 1997, Annals of human genetics.

[11]  J. Terwilliger,et al.  Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12 , 1996, Nature Genetics.

[12]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[13]  K Lange,et al.  Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. , 1996, American journal of human genetics.

[14]  A. Whittemore,et al.  A class of tests for linkage using affected pedigree members. , 1994, Biometrics.

[15]  N. Risch Linkage strategies for genetically complex traits. I. Multilocus models. , 1990, American journal of human genetics.

[16]  J. Ott Analysis of Human Genetic Linkage , 1985 .

[17]  B. Suarez,et al.  A simple method to detect linkage for rare recessive diseases: An application to juvenile diabetes , 1979, Clinical genetics.

[18]  Kyunghee K. Song,et al.  Comparison of allele‐sharing statistics for general pedigrees , 2000, Genetic epidemiology.

[19]  M S McPeek,et al.  Optimal allele‐sharing statistics for genetic mapping using affected relatives , 1999, Genetic epidemiology.

[20]  L. Abel,et al.  Comparison of four sib‐pair linkage methods for analyzing sibships with more than two affecteds: Interest of the binomial maximum likelihood approach , 1998, Genetic epidemiology.

[21]  E. Thompson,et al.  Genetic mapping of disease genes , 1997 .

[22]  S A Seuchter,et al.  Linkage analysis in nuclear families. 1: Optimality criteria for affected sib-pair tests. , 1994, Human heredity.

[23]  K. Lange,et al.  Programs for pedigree analysis: Mendel, Fisher, and dGene , 1988, Genetic epidemiology.

[24]  Blackwelder Wc,et al.  A comparison of sib-pair linkage tests for disease susceptibility loci , 1985 .

[25]  R. Elston,et al.  A comparison of sib‐pair linkage tests for disease susceptibility loci , 1985, Genetic epidemiology.