Evidence map›Paper›PMID 30987598›Full record

ArticleBMC bioinformatics2019

Highly efficient hypothesis testing methods for regression-type tests with correlated observations and heterogeneous variance structure.

Yun Zhang, Gautam Bandyopadhyay, David J Topham, Ann R Falsey, Xing Qiu

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 1 country.

Yun ZhangJ Craig Venter Institute, 4120 Capricorn Lane, La Jolla 92037, CA, USA.
Gautam BandyopadhyayDepartment of Surgery, University of Rochester, 601 Elmwood Ave, Rochester, Rochester 14642, NY, USA.
David J TophamDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Ave, Rochester, Rochester 14642, NY, USA.
Ann R FalseyDepartment of Medicine, University of Rochester, 601 Elmwood Ave, Rochester, Rochester 14642, NY, USA.
Xing QiuDepartment of Biostatistics and Computational Biology, University of Rochester, 601 Elmwood Ave, Rochester, Rochester 14642, NY, USA. Xing_Qiu@urmc.rochester.edu.ORCID http://orcid.org/0000-0002-2330-3544
University of Rochester · USJ. Craig Venter Institute · USUniversity of Rochester Medical Center · US

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
TRAINING IN ENVIRONMENTAL HEALTH SCIENCES BIOSTATISTICST32ES007271 · NIEHS · UNIVERSITY OF ROCHESTER · PI Sally W Thurston · 1992 to 2026
$3.9M
NCATS NIH HHS UL1 TR002001NIAID NIH HHS HHSN272201200005CNIAID NIH HHS P30 AI078498NIEHS NIH HHS T32 ES007271NIEHS NIH HHS T32ES007271NIH HHS NIH 5 P30 AI078498-08
6 · The paper itself

Abstract

backgroundFor many practical hypothesis testing (H-T) applications, the data are correlated and/or with heterogeneous variance structure. The regression t-test for weighted linear mixed-effects regression (LMER) is a legitimate choice because it accounts for complex covariance structure; however, high computational costs and occasional convergence issues make it impractical for analyzing high-throughput data. In this paper, we propose computationally efficient parametric and semiparametric tests based on a set of specialized matrix techniques dubbed as the PB-transformation. The PB-transformation has two advantages: 1. The PB-transformed data will have a scalar variance-covariance matrix. 2. The original H-T problem will be reduced to an equivalent one-sample H-T problem. The transformed problem can then be approached by either the one-sample Student's t-test or Wilcoxon signed rank test.

resultsIn simulation studies, the proposed methods outperform commonly used alternative methods under both normal and double exponential distributions. In particular, the PB-transformed t-test produces notably better results than the weighted LMER test, especially in the high correlation case, using only a small fraction of computational cost (3 versus 933 s). We apply these two methods to a set of RNA-seq gene expression data collected in a breast cancer study. Pathway analyses show that the PB-transformed t-test reveals more biologically relevant findings in relation to breast cancer than the weighted LMER test.

conclusionsAs fast and numerically stable replacements for the weighted LMER test, the PB-transformed tests are especially suitable for "messy" high-throughput data that include both independent and matched/repeated samples. By using our method, the practitioners no longer have to choose between using partial data (applying paired tests to only the matched samples) or ignoring the correlation in the data (applying two sample tests to data with some correlated samples). Our method is implemented as an R package 'PBtest' and is available at https://github.com/yunzhang813/PBtest-R-Package .

Indexed as

Breast NeoplasmsComputer SimulationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansModels, GeneticRegression AnalysisROC CurveHypothesis testingMatrix decompositionOrthogonal transformationRNA-seqRotated test

Identifiers

PMID30987598
PMCPMC6466736
OpenAlexW2911249570

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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 OpenQuestion graph.