ArticleAmerican journal of human genetics2000
Composite statistics for QTL mapping with moderately discordant sibling pairs.
Article in American journal of human genetics, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 39 citations in OpenAlex.
- A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.Molecular psychiatry · 2005Trial
- Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2013Article
- Impact on modes of inheritance and relative risks of using extreme sampling when designing genetic association studies.Annals of human genetics · 2013Article
- Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.Behavior genetics · 2011Article
- Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.Human genetics · 2009Article
- Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.Behavior genetics · 2008Article
- Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis.American journal of human genetics · 2005Article
- Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods.Molecular biotechnology · 2004Review
- A powerful and robust new linkage statistic for discordant sibling pairs.American journal of human genetics · 2004Article
- Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.American journal of human genetics · 2004Article
- Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.Human genetics · 2003Article
- Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs.American journal of human genetics · 2003Article
- Powerful regression-based quantitative-trait linkage analysis of general pedigrees.American journal of human genetics · 2002Article
Corrections and comments
- Erratum issued
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
Extreme discordant sibling-pair (EDSP) designs have been shown in theory to be very powerful for mapping quantitative-trait loci (QTLs) in humans. However, their practical applicability has been somewhat limited by the need to phenotype very large populations to find enough pairs that are extremely discordant. In this paper, we demonstrate that there is also substantial power in pairs that are only moderately discordant, and that designs using moderately discordant pairs can yield a more practical balance between phenotyping and genotyping efforts. The power we demonstrate for moderately discordant pairs stems from a new statistical result. Statistical analysis in discordant-pair studies is generally done by testing for reduced identity by descent (IBD) sharing in the pairs. By contrast, the most commonly-used statistical methods for more standard QTL mapping are Haseman-Elston regression and variance-components analysis. Both of these use statistics that are functions of the trait values given IBD information for the pedigree. We show that IBD sharing statistics and "trait value given IBD" statistics contribute complementary rather than redundant information, and thus that statistics of the two types can be combined to form more powerful tests of linkage. We propose a simple composite statistic, and test it with simulation studies. The simulation results show that our composite statistic increases power only minimally for extremely discordant pairs. However, it boosts the power of moderately discordant pairs substantially and makes them a very practical alternative. Our composite statistic is straightforward to calculate with existing software; we give a practical example of its use by applying it to a Genetic Analysis Workshop (GAW) data set.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.