Evidence map›Paper›PMID 19622101›Full record

ArticleAnnals of human genetics2009

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity.

Youfang Liu, Yi-Ju Li, Glen A Satten, Andrew S Allen, Jung-Ying Tzeng

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Annals of human genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. New Genetic Approaches to AD: Lessons from APOE-TOMM40 Phylogenetics.Current neurology and neuroscience reports · 2016
    Review
  2. Article
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Youfang LiuBioinformatics Research Center, North Carolina State University, Raleigh, NC 27569-7566, USA.
Yi-Ju Li
Glen A Satten
Andrew S Allen
Jung-Ying Tzeng
North Carolina State University · USCenter for Human Genetics · USCenters for Disease Control and Prevention · USDuke University · US

Funding

FAMILIAL AND BIRTH COHORT EFFECTS ON THE AGING SENSESR01AG021917 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI CRUICKSHANKS, KAREN J · 2004 to 2018
$25.2M
GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
Investigation of the Genetics of AsthmaR01HL049609 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLUMENTHAL, MALCOLM NOLAN · 2003 to 2006
$3.1M
Genome-wide Haplotype Association Analysis in Mental DisordersR01MH084022 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TZENG, JUNG-YING · 2009 to 2011
$1.1M
NHLBI NIH HHS 5R01-HL049609-14NHLBI NIH HHS R01 HL049609NIA NIH HHS 1R01-AG021917-01A1NIA NIH HHS R01 AG021917NIGMS NIH HHS R01 GM031575NIGMS NIH HHS R01-GM031575NIMH NIH HHS R01 MH084022NIMH NIH HHS R01MH084022-01A1
6 · The paper itself

Abstract

Association methods based on haplotype similarity (HS) can overcome power and stability issues encountered in standard haplotype analyses. Current HS methods can be generally classified into evolutionary and two-sample approaches. We propose a new regression-based HS association method for case-control studies that incorporates covariate information and combines the advantages of the two classes of approaches by using inferred ancestral haplotypes. We first estimate the ancestral haplotypes of case individuals and then, for each individual, an ancestral-haplotype-based similarity score is computed by comparing that individual's observed genotype with the estimated ancestral haplotypes. Trait values are then regressed on the similarity scores. Covariates can easily be incorporated into this regression framework. To account for the bias in the raw p-values due to the use of case data in constructing ancestral haplotypes, as well as to account for variation in ancestral haplotype estimation, a permutation procedure is adopted to obtain empirical p-values. Compared with the standard haplotype score test and the multilocus T(2) test, our method improves power when neither the allele frequency nor linkage disequilibrium between the disease locus and its neighboring SNPs is too low and is comparable in other scenarios. We applied our method to the Genetic Analysis Workshop 15 simulated SNP data and successfully pinpointed a stretch of SNPs that covers the fine-scale region where the causal locus is located.

Indexed as

Case-Control StudiesGenetic TechniquesRegression AnalysisComputer SimulationGene FrequencyGenome, HumanHaplotypesHumansLinkage DisequilibriumModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID19622101
PMCPMC2747372
OpenAlexW1985559230

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.