Evidence map›Paper›PMID 20976795›Full record

ArticleGenetic epidemiology2010

Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression.

Fang Han, Wei Pan

Abstract read
In one paragraph

Article in Genetic epidemiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

2 authors.

Fang HanDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota 55455–0392, USA.
Wei Pan

Funding

New Machine Learning Tools for Biomedical DataR01GM081535 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2007 to 2014
$2.2M
Statistical Methods for Genomic and Proteomic DataR01HL065462 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI PAN, WEI · 2002 to 2012
$1.5M
NHLBI NIH HHS HL65462NHLBI NIH HHS R01 HL065462NIGMS NIH HHS GM081535NIGMS NIH HHS R01 GM081535
6 · The paper itself

Abstract

To detect genetic association with common and complex diseases, many statistical tests have been proposed for candidate gene or genome-wide association studies with the case-control design. Due to linkage disequilibrium (LD), multi-marker association tests can gain power over single-marker tests with a Bonferroni multiple testing adjustment. Among many existing multi-marker association tests, most target to detect only one of many possible aspects in distributional differences between the genotypes of cases and controls, such as allele frequency differences, while a few new ones aim to target two or three aspects, all of which can be implemented in logistic regression. In contrast to logistic regression, a genomic distance-based regression (GDBR) approach aims to detect some high-order genotypic differences between cases and controls. A recent study has confirmed the high power of GDBR tests. At this moment, the popular logistic regression and the emerging GDBR approaches are completely unrelated; for example, one has to choose between the two. In this article, we reformulate GDBR as logistic regression, opening a venue to constructing other powerful tests while overcoming some limitations of GDBR. For example, asymptotic distributions can replace time-consuming permutations for deriving P-values and covariates, including gene-gene interactions, can be easily incorporated. Importantly, this reformulation facilitates combining GDBR with other existing methods in a unified framework of logistic regression. In particular, we show that Fisher's P-value combining method can boost statistical power by incorporating information from allele frequencies, Hardy-Weinberg disequilibrium, LD patterns, and other higher-order interactions among multi-markers as captured by GDBR.

Indexed as

Logistic ModelsModels, GeneticAllelesAmyotrophic Lateral SclerosisComputer SimulationGene FrequencyGenetic MarkersGenome-Wide Association StudyHumansLinkage DisequilibriumMolecular EpidemiologyPolymorphism, Single NucleotideRegression AnalysisGenetic Markers

Identifiers

PMID20976795
PMCPMC3345567

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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.