Evidence map›Paper›PMID 18215207›Full record

ArticleAnnals of human genetics2008

Optimal two-stage design for case-control association analysis incorporating genotyping errors.

Y Zuo, G Zou, J Wang, H Zhao, H Liang

Abstract read
In one paragraph

Article in Annals of human genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Y ZuoDepartment of Statistics and Probability, Michigan State University, East Lansing, MI 48824, USA.
G Zou
J Wang
H Zhao
H Liang

Funding

STATISTICAL METHODS TO MAP GENES FOR COMPLEX TRAITSR01GM059507 · NIGMS · YALE UNIVERSITY · PI ZHAO, HONGYU · 1999 to 2013
$3.6M
Analysis of AIDS Data by Using Semiparametrical ModelsR01AI062247 · NIAID · UNIVERSITY OF ROCHESTER · PI LIANG, HUA · 2004 to 2006
$578k
Generalized Varying-Coefficient Partially Linear ModelsR01AI059773 · NIAID · UNIVERSITY OF ROCHESTER · PI LIANG, HUA · 2005 to 2007
$568k
NIAID NIH HHS AI59773NIAID NIH HHS AI62247-01NIAID NIH HHS R01 AI059773NIAID NIH HHS R01 AI062247NIGMS NIH HHS GM59507NIGMS NIH HHS R01 GM059507
6 · The paper itself

Abstract

Two-stage design is a cost effective approach for identifying disease genes in genetic studies and it has received much attention recently. In general, there are two types of two-stage designs that differ on the methods and samples used to measure allele frequencies in the first stage: (1) Individual genotyping is used in the first stage; (2) DNA pooling is used in the first stage. In this paper, we focus on the latter. Zuo et al. (2006) investigated statistical power of such a design, among other things, but the cost of the study was not taken into account. The purpose of this paper is to study the optimal design under the given overall cost. We investigate how to allocate the resources to the two stages. Note that in addition to the measurement errors associated with DNA pooling, genotyping errors are also unavoidable with individual genotyping. Therefore, we discuss the optimal design combining genotyping errors associated with individual genotyping. The joint statistical distributions of test statistics in the first and second stages are derived. For a fixed cost, our results show that the optimal design requires no additional samples in the second stage but only that the samples in the first stage be re-used. When the second stage uses an entirely independent sample, however, the optimal design under a given cost depends on the population allele frequency and allele frequency difference between the case and control groups. For the current genotyping costs, we can roughly allocate 1/3 to 1/2 of the total sample size to the first stage for screening.

Indexed as

Case-Control StudiesGenetic Predisposition to DiseaseGenetic TechniquesGene FrequencyHumansModels, GeneticResearch Design

Identifiers

PMID18215207
PMCPMC2836813

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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.