Cost-effective analysis of candidate genes using htSNPs: a staged approach

We have previously shown that the selection of haplotype tag single nucleotide polymorphisms (htSNPs) and their statistical analysis in a multi-locus transmission/disequilibrium test (TDT) results in a more cost-effective genotyping strategy in disease association studies of genes by minimising redundancy due to linkage disequilibrium between SNPs. Further savings can be achieved by the use of a two-stage genotyping strategy. This approach is illustrated here in conjunction with the multi-locus TDT in determining whether common alleles of the immune regulatory genes RANK and its ligand TRANCE (RANKL) are associated with type 1 diabetes (T1D). A saving of approximately 75% of potential genotyping reactions could be made with minimal loss of power. There was little evidence from our analysis for association between the TRANCE and RANK genes and T1D in the populations tested.

[1]  D. Boos On Generalized Score Tests , 1992 .

[2]  J. Todd,et al.  Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases. , 2001, Diabetes.

[3]  H Zhao,et al.  Group sequential methods and sample size savings in biomarker-disease association studies. , 2003, Genetics.

[4]  M. Waterman,et al.  A dynamic programming algorithm for haplotype block partitioning , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Thomas A Trikalinos,et al.  Genetic associations in large versus small studies: an empirical assessment , 2003, The Lancet.

[6]  R. Elston,et al.  Optimal two‐stage genotyping in population‐based association studies , 2003, Genetic epidemiology.

[7]  Christopher A. Haiman,et al.  Choosing Haplotype-Tagging SNPS Based on Unphased Genotype Data Using a Preliminary Sample of Unrelated Subjects with an Example from the Multiethnic Cohort Study , 2003, Human Heredity.

[8]  R. Flavell,et al.  Pancreatic lymph node-derived CD4(+)CD25(+) Treg cells: highly potent regulators of diabetes that require TRANCE-RANK signals. , 2002, Immunity.

[9]  S. Pearce,et al.  Evidence for a new Graves disease susceptibility locus at chromosome 18q21. , 2000, American journal of human genetics.

[10]  J. Todd,et al.  Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21. , 1997, Human molecular genetics.

[11]  Xiangli Xiao,et al.  Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. , 2003, Arthritis and rheumatism.

[12]  Lon R. Cardon,et al.  Efficient selective screening of haplotype tag SNPs , 2003, Bioinform..

[13]  Frank Dudbridge,et al.  Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.

[14]  Juliet M Chapman,et al.  Detecting Disease Associations due to Linkage Disequilibrium Using Haplotype Tags: A Class of Tests and the Determinants of Statistical Power , 2003, Human Heredity.

[15]  Ruzong Fan,et al.  Genome association studies of complex diseases by case-control designs. , 2003, American journal of human genetics.

[16]  Nelson B Freimer,et al.  Cost-effective designs for linkage disequilibrium mapping of complex traits. , 2003, American journal of human genetics.