Evidence map›Paper›PMID 19503792›Full record

ArticlePloS one2009

A kinship-based modification of the armitage trend test to address hidden population structure and small differential genotyping errors.

Cyril S Rakovski, Daniel O Stram

Abstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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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

13 citing papers in PubMed.

  1. Article
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  10. Review
  11. Exploring genetic susceptibility to cancer in diverse populations.Current opinion in genetics & development · 2010
    Review
  12. Article
  13. 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

2 authors.

Cyril S RakovskiDepartment of Mathematics and Computer Science, Chapman University, Orange, California, United States of America. rakovski@chapman.edu
Daniel O Stram

Funding

Implications of haplotype structure in the human genomeP50HG002790 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAVARE, SIMON · 2003 to 2013
$29.9M
USC CANCER EPIDEMIOLOGY &BIOSTATISTICS UNITP01CA017054 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HAIMAN, CHRISTOPHER ALAN · 1985 to 2009
$18.2M
Computational Methods for Fine MappingR01GM069890 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MARJORAM, PAUL · 2004 to 2007
$1.9M
NCI NIH HHS P01 CA017054NCI NIH HHS P01 CA17054-27A2NHGRI NIH HHS P50 HG002790NHGRI NIH HHS P50 HG002790-01A1NHLBI NIH HHS U01 HL084705-01NIGMS NIH HHS R01 GM069890NIGMS NIH HHS R01 GM069890-01A1
6 · The paper itself

Abstract

BACKGROUND/

aimsWe propose a modification of the well-known Armitage trend test to address the problems associated with hidden population structure and hidden relatedness in genome-wide case-control association studies.

methodsThe new test adopts beneficial traits from three existing testing strategies: the principal components, mixed model, and genomic control while avoiding some of their disadvantageous characteristics, such as the tendency of the principal components method to over-correct in certain situations or the failure of the genomic control approach to reorder the adjusted tests based on their degree of alignment with the underlying hidden structure. The new procedure is based on Gauss-Markov estimators derived from a straightforward linear model with an imposed variance structure proportional to an empirical relatedness matrix. Lastly, conceptual and analytical similarities to and distinctions from other approaches are emphasized throughout.

resultsOur simulations show that the power performance of the proposed test is quite promising compared to the considered competing strategies. The power gains are especially large when small differential differences between cases and controls are present; a likely scenario when public controls are used in multiple studies.

conclusionThe proposed modified approach attains high power more consistently than that of the existing commonly implemented tests. Its performance improvement is most apparent when small but detectable systematic differences between cases and controls exist.

Indexed as

GenotypeResearch DesignAllelesCase-Control StudiesComputer SimulationGene FrequencyHumansMarkov ChainsModels, StatisticalModels, TheoreticalPrincipal Component AnalysisReproducibility of Results

Identifiers

PMID19503792
PMCPMC2688076

What Socratic holds

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LicenceCC BY
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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 Socratic graph.