𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Use of unphased multilocus genotype data in indirect association studies

✍ Scribed by David Clayton; Juliet Chapman; Jason Cooper


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
165 KB
Volume
27
Category
Article
ISSN
0741-0395

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

It is usually assumed that detection of a disease susceptability gene via marker polymorphisms in linkage disequilibrium with it is facilitated by consideration of marker haplotypes. However, capture of the marker haplotype information requires resolution of gametic phase, and this must usually be inferred statistically. Recently, we questioned the value of the marker haplotype information, and suggested that certain analyses of multivariate marker data, not based on haplotypes explicitly and not requiring resolution of gametic phase, are often more powerful than analyses based on haplotypes. Here, we review this work and assess more carefully the situations in which our conclusions might apply. We also relate these analyses to alternative approaches to haplotype analysis, namely those based on haplotype similarity and those inspired by cladistics. Β© 2004 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Direct analysis of unphased SNP genotype
✍ Andrew P. Morris πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 212 KB πŸ‘ 1 views

We describe a novel method for assessing the strength of disease association with single nucleotide polymorphisms (SNPs) in a candidate gene or small candidate region, and for estimating the corresponding haplotype relative risks of disease, using unphased genotype data directly. We begin by estimat

Streamlined analysis of pooled genotype
✍ Valentina Moskvina; Nadine Norton; Nigel Williams; Peter Holmans; Michael Owen; πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 130 KB πŸ‘ 1 views

## Abstract Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and cheap way for detecting allelic association between genetic markers and disease. To obtain accurate estimates of allele frequencies, a correction factor __k__ for the degree to which measu

Use of longitudinal data in genetic stud
✍ Berit Kerner; Kari E. North; M. Daniele Fallin πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 87 KB πŸ‘ 2 views

## Abstract Participants analyzed actual and simulated longitudinal data from the Framingham Heart Study for various metabolic and cardiovascular traits. The genetic information incorporated into these investigations ranged from selected single‐nucleotide polymorphisms to genome‐wide association ar

Meta-analysis of genome-wide association
✍ D. Y. Lin; D. Zeng πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 295 KB πŸ‘ 2 views

## Abstract To identify genetic variants with modest effects on complex human diseases, a growing number of networks or consortia are created for sharing data from multiple genome‐wide association studies on the same disease or related disorders. A central question in this enterprise is whether to

Comparison of SNP tagging methods using
✍ Peter B. Chi; Priya Duggal; W.H. Linda Kao; Rasika A. Mathias; Audrey V. Grant; πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 349 KB πŸ‘ 2 views

## Abstract Few comparison studies have been performed on single nucleotide polymorphism (SNP) tagging methods to examine their consistency and effectiveness in terms of inferences about association with disease. We applied several SNP tagging methods to SNPs on chromosome 12q (__n__=713) and compa