Parsing the effects of individual SNPs in candidate genes with family data

Hum Hered. 2010;69(2):91-103. doi: 10.1159/000264447. Epub 2009 Dec 4.

Abstract

We introduce a stepwise approach for family-based designs for selecting a set of markers in a gene that are independently associated with the disease. The approach is based on testing the effect of a set of markers conditional on another set of markers. Several likelihood-based approaches have been proposed for special cases, but no model-free based tests have been proposed. We propose two types of tests in a family-based framework that are applicable to arbitrary family structures and completely robust to population stratification. We propose methods for ascertained dichotomous traits and unascertained quantitative traits. We first propose a completely model-free extension of the FBAT main genetic effect test. Then, for power issues, we introduce two model-based tests, one for dichotomous traits and one for continuous traits. Lastly, we utilize these tests to analyze a continuous lung function phenotype as a proxy for asthma in the Childhood Asthma Management Program. The methods are implemented in the free R package fbati.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma / genetics*
  • Family
  • Genetic Predisposition to Disease*
  • Humans
  • Interleukin-10 / genetics
  • Models, Genetic
  • Polymorphism, Single Nucleotide*
  • Software

Substances

  • IL10 protein, human
  • Interleukin-10