Evidence map›Paper›PMID 26436424›Full record

ArticlePloS one2015

Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.

Brandon Coombes, Saonli Basu, Sharmistha Guha, Nicholas Schork

Abstract read
In one paragraph

Article in PloS one, 2015. 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
–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

4 citing papers in PubMed.

  1. [An improved association analysis pipeline for tumor susceptibility variant in haplotype amplification area].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
  2. Article
  3. Estimation of QT interval prolongation through model-averaging.Journal of pharmacokinetics and pharmacodynamics · 2017
    Article
  4. 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

4 authors.

Brandon CoombesDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, United States of America.
Saonli BasuDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, United States of America.
Sharmistha GuhaDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, United States of America.
Nicholas SchorkJ. Craig Venter Institute, La Jolla, CA, United States of America.

Funding

Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI NICHOLAS Joseph SCHORK · 2004 to 2026
$102.6M
Statistical Methods for detection of genome-wide GxE interactions in longitudinalR01DA033958 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2013 to 2016
$1.1M
Biostatistics in Genetics and Genomics Training ProgramT32GM108557 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2014 to 2018
$583k
NIA NIH HHS U19 AG023122NIDA NIH HHS R01 DA033958NIDA NIH HHS SB R01DA033958NIGMS NIH HHS T32 GM108557NIGMS NIH HHS T32GM108557
6 · The paper itself

Abstract

Multi-locus effect modeling is a powerful approach for detection of genes influencing a complex disease. Especially for rare variants, we need to analyze multiple variants together to achieve adequate power for detection. In this paper, we propose several parsimonious branching model techniques to assess the joint effect of a group of rare variants in a case-control study. These models implement a data reduction strategy within a likelihood framework and use a weighted score test to assess the statistical significance of the effect of the group of variants on the disease. The primary advantage of the proposed approach is that it performs model-averaging over a substantially smaller set of models supported by the data and thus gains power to detect multi-locus effects. We illustrate these proposed approaches on simulated and real data and study their performance compared to several existing rare variant detection approaches. The primary goal of this paper is to assess if there is any gain in power to detect association by averaging over a number of models instead of selecting the best model. Extensive simulations and real data application demonstrate the advantage the proposed approach in presence of causal variants with opposite directional effects along with a moderate number of null variants in linkage disequilibrium.

Indexed as

AlgorithmsCase-Control StudiesComputer SimulationGenetic VariationModels, GeneticAllelesAmidohydrolasesFatty Acid Amide HydrolasesGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansMonoacylglycerol LipasesPolymorphism, Single NucleotideAmidohydrolasesFatty Acid Amide HydrolasesMonoacylglycerol Lipases

Identifiers

PMID26436424
PMCPMC4593572

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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.