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Disa Yu

dblp:234/6465 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2020
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis › microarray data preprocessing
cross-platform normalization
0.412020
MatchMixeR: a cross-platform normalization method for gene expression data integration · Bioinform. 2020
Bioinformatics and computational biology › multi-omics data integration
gene expression data integration
0.412020
MatchMixeR: a cross-platform normalization method for gene expression data integration · Bioinform. 2020
Bioinformatics and computational biology › gene expression analysis
differential expression analysis
0.112020
MatchMixeR: a cross-platform normalization method for gene expression data integration · Bioinform. 2020

Methods — techniques the papers use, named apart from their topics

moment method · 0.4linear mixed effects regression · 0.4
YearPublicationVenuePosition
2020 MatchMixeR: a cross-platform normalization method for gene expression data integration
abstract
MOTIVATION: Combining 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. RESULTS: Compared 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.
Serin Zhang, Disa Yu, Xing Qiu
Bioinform.3