Evidence map›Paper›PMID 26653287›Full record

ArticleBMC genomics2015

Incorporation of subject-level covariates in quantile normalization of miRNA data.

Anvar Suyundikov, John R Stevens, Christopher Corcoran, Jennifer Herrick, Roger K Wolff, Martha L Slattery

Abstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

6 authors.

Anvar SuyundikovDepartment of Mathematics and Statistics, Utah State University, 3900 Old Main Hill, Logan, 84322-3900, UT, U.S.A. asu@biostatsolutions.com.
John R StevensDepartment of Mathematics and Statistics, Utah State University, 3900 Old Main Hill, Logan, 84322-3900, UT, U.S.A. john.r.stevens@usu.edu.
Christopher CorcoranDepartment of Mathematics and Statistics, Utah State University, 3900 Old Main Hill, Logan, 84322-3900, UT, U.S.A. chris.corcoran@usu.edu.
Jennifer HerrickDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, 383 Colorow Road, Salt Lake City, 84108, UT, U.S.A. jennifer.herrick@hsc.utah.edu.
Roger K WolffDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, 383 Colorow Road, Salt Lake City, 84108, UT, U.S.A. roger.wolff@hsc.utah.edu.
Martha L SlatteryDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, 383 Colorow Road, Salt Lake City, 84108, UT, U.S.A. marty.slattery@hsc.utah.edu.

Funding

miRNA and colorectal cancer: associations with tumor phenotype and survivalR01CA163683 · NCI · UNIVERSITY OF UTAH · PI SLATTERY, MARTHA L · 2012 to 2017
$6.5M
NCI NIH HHS 1R01CA163683-01A1NCI NIH HHS R01 CA163683
6 · The paper itself

Abstract

backgroundMost currently-used normalization methods for miRNA array data are based on methods developed for mRNA arrays despite fundamental differences between the data characteristics. The application of conventional quantile normalization can mask important expression differences by ignoring demographic and environmental factors. We present a generalization of the conventional quantile normalization method, making use of available subject-level covariates in a colorectal cancer study.

resultsIn simulation, our weighted quantile normalization method is shown to increase statistical power by as much as 10 % when relevant subject-level covariates are available. In application to the colorectal cancer study, this increase in power is also observed, and previously-reported dysregulated miRNAs are rediscovered.

conclusionsWhen any subject-level covariates are available, the weighted quantile normalization method should be used over the conventional quantile normalization method.

Indexed as

AgedAlgorithmsColorectal NeoplasmsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMicroRNAsMiddle AgedModels, GeneticModels, StatisticalMicroRNAs

Identifiers

PMID26653287
PMCPMC4675058

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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.