Evidence map›Paper›PMID 31904810›Full record

ArticleBioinformatics (Oxford, England)2020

MatchMixeR: a cross-platform normalization method for gene expression data integration.

Serin Zhang, Jiang Shao, Disa Yu, Xing Qiu, Jinfeng Zhang

Abstract read
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Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Serin ZhangDepartment of Statistics, Florida State University, Tallahassee, FL 32306, USA.
Jiang ShaoGilead Sciences Inc., Foster City, CA 94404, USA.
Disa YuDepartment of Statistics, Florida State University, Tallahassee, FL 32306, USA.
Xing QiuDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY 14624, USA.
Jinfeng ZhangDepartment of Statistics, Florida State University, Tallahassee, FL 32306, USA.

Funding

Collaborative Research: Mathematical Framework for Biomolecules: From Protein to RNA to ChromosomesR01GM126558 · NIGMS · FLORIDA STATE UNIVERSITY · PI ZHANG, JINFENG · 2017 to 2021
$1.5M
NIGMS NIH HHS R01 GM126558
6 · The paper itself

Abstract

motivationCombining gene expression (GE) profiles generated from different platforms enables previously infeasible studies due to sample size limitations. Several cross-platform normalization methods have been developed to remove the systematic differences between platforms, but they may also remove meaningful biological differences among datasets. In this work, we propose a novel approach that removes the platform, not the biological differences. Dubbed as 'MatchMixeR', we model platform differences by a linear mixed effects regression (LMER) model, and estimate them from matched GE profiles of the same cell line or tissue measured on different platforms. The resulting model can then be used to remove platform differences in other datasets. By using LMER, we achieve better bias-variance trade-off in parameter estimation. We also design a computationally efficient algorithm based on the moment method, which is ideal for ultra-high-dimensional LMER analysis.

resultsCompared with several prominent competing methods, MatchMixeR achieved the highest after-normalization concordance. Subsequent differential expression analyses based on datasets integrated from different platforms showed that using MatchMixeR achieved the best trade-off between true and false discoveries, and this advantage is more apparent in datasets with limited samples or unbalanced group proportions. AVAILABILITY AND IMPLEMENTATION: Our method is implemented in a R-package, 'MatchMixeR', freely available at: https://github.com/dy16b/Cross-Platform-Normalization. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsGene Expression ProfilingGene ExpressionResearch Design

Identifiers

PMID31904810
PMCPMC7868049

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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.