Evidence map›Paper›PMID 16816420›Full record

ArticleGenetics2006

Nonlinear tests for genomewide association studies.

Jinying Zhao, Li Jin, Momiao Xiong

Abstract readComparative Study
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Human genetics of diabetic retinopathy.Journal of endocrinological investigation · 2014
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
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

3 authors.

Jinying ZhaoHuman Genetics Center, University of Texas Health Science Center, Houston 77030, USA.
Li Jin
Momiao Xiong

Funding

Role of TGF-beta and CTGF Signaling Transgenic Mouse Models of SclerodermaP50AR054144 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CROMBRUGGHE, BENOIT DE · 2006 to 2010
$7.7M
Transgenic animal models for fibrotic diseaseP50AR044888 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARNETT, FRANK C · 1997 to 2005
$6.6M
Anthipertensive PharmacoGenomicsR01HL074735 · NHLBI · MAYO CLINIC ROCHESTER · PI TURNER, STEPHEN T · 2003 to 2006
$3.4M
Positional Gene Identification of Complex TraitsR01ES009912 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMOS, CHRISTOPHER I. · 1999 to 2006
$3.3M
NHLBI NIH HHS HL74735NHLBI NIH HHS R01 HL074735NIAMS NIH HHS 1P50AR44888NIAMS NIH HHS P50 AR044888NIAMS NIH HHS P50 AR054144NIEHS NIH HHS ES09912NIEHS NIH HHS R01 ES009912
6 · The paper itself

Abstract

As millions of single-nucleotide polymorphisms (SNPs) have been identified and high-throughput genotyping technologies have been rapidly developed, large-scale genomewide association studies are soon within reach. However, since a genomewide association study involves a large number of SNPs it is therefore nearly impossible to ensure a genomewide significance level of 0.05 using the available statistics, although the multiple-test problems can be alleviated, but not sufficiently, by the use of tagging SNPs. One strategy to circumvent the multiple-test problem associated with genome-wide association tests is to develop novel test statistics with high power. In this report, we introduce several nonlinear tests, which are based on nonlinear transformation of allele or haplotype frequencies. We investigate the power of the nonlinear test statistics and demonstrate that under certain conditions, some nonlinear test statistics have much higher power than the standard chi2-test statistic. Type I error rates of the nonlinear tests are validated using simulation studies. We also show that a class of similarity measure-based test statistics is based on the quadratic function of allele or haplotype frequencies, and thus they belong to nonlinear tests. To evaluate their performance, the nonlinear test statistics are also applied to three real data sets. Our study shows that nonlinear test statistics have great potential in association studies of complex diseases.

Indexed as

Genome, HumanModels, StatisticalAcyltransferasesAllelesCatechol O-MethyltransferaseComputer SimulationEsophageal NeoplasmsFemaleGene FrequencyHaplotypesHumansMaleMatrix Metalloproteinase 2Membrane ProteinsPolymorphism, Single NucleotideReproducibility of ResultsAcyltransferasesCatechol O-MethyltransferaseMatrix Metalloproteinase 2Membrane ProteinsZDHHC8 protein, human

Identifiers

PMID16816420
PMCPMC1667094

What OpenQuestion holds

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Registered trials

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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.