𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Exact family-based association tests for biallelic data

✍ Scribed by Kady Schneiter; Nan Laird; Chris Corcoran


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
134 KB
Volume
29
Category
Article
ISSN
0741-0395

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Family‐based study designs have an important role in the search for association between disease phenotypes and genetic markers. Unlike traditional case‐control methods, family‐based tests use within‐family data to avoid identification of spurious associations that may result from population admixture. Many family‐based association tests have been proposed to accommodate a variety of ascertainment schemes and patterns of missing data. In this report, we describe exact family‐based association tests for biallelic data. Specifically, we discuss test of the null hypotheses “no linkage and no association” and “linkage, but no association”. These tests, which are valid under various models for inheritance and patterns of missingness, utilize the procedure proposed by Rabinowitz and Laird [2000: Hum Hered 50:211–223] that provides a unified framework for family based association testing (FBAT). The conditioning approach implemented in FBAT makes an exact test conceptually straightforward, but computationally difficult since the minimum sufficient statistics upon which we condition do not have a conventional form. An exact test may be especially critical when accurate computation of the extreme area of the FBAT statistic is needed, such as when the study design necessitates multiple comparisons adjustments. We describe the exact approach as a useful alternative to the aymptotic test and show that the exact tests for biallelic data may be most useful for the recessive disease model. Genet. Epidemiol. 2005 © 2005 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Tests for genetic association using fami
✍ Mei-Chiung Shih; Alice S. Whittemore 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 102 KB 👁 1 views

We use likelihood-based score statistics to test for association between a disease and a diallelic polymorphism, based on data from arbitrary types of nuclear families. The Nonfounder statistic extends the transmission disequilibrium test (TDT) to accommodate affected and unaffected offspring, missi

A general class of association tests for
✍ Xin Liu; Derek Gordon 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 190 KB 👁 1 views

## Abstract Based on the symmetry of transmitted/nontransmitted alleles from heterozygous parents under the null hypothesis of no association, the work proposed here establishes a general statistical framework for constructing association tests with data from nuclear families with multiple affected

Family-based association tests for ordin
✍ Xueqin Wang; Yuanqing Ye; Heping Zhang 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB 👁 1 views

## Abstract We present a class of family‐based association tests (FBATs) for ordinal traits that adjust for the effects of covariates. For complex diseases, especially mental health conditions including nicotine dependence and substance use, the outcome variables are often recorded in an ordinal ra

Genetic association tests for family dat
✍ Alice S. Whittemore; Jerry Halpern 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 151 KB 👁 2 views

## Abstract We consider three tests for genetic association in data from nuclear families (the Family‐Based Association Test (FBAT) test proposed by Rabinowitz and Laird ([2000] Hum. Hered. 50:211–223), a second test proposed by Rabinowitz ([2002] J. Am. Stat. Assoc. 97:742–758), and the Family Gen

Family-based tests for associating haplo
✍ Steve Horvath; Xin Xu; Stephen L. Lake; Edwin K. Silverman; Scott T. Weiss; Nan 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 122 KB 👁 2 views

## Abstract We provide a general purpose family‐based testing strategy for associating disease phenotypes with haplotypes when phase may be ambiguous and parental genotype data may be missing. These tests for linkage and association can be used in candidate gene studies with tightly linked markers.