Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Darlene Lu

dblp:236/6534 · DBLP profile ↗
← Back
1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

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
0.412019
Clustering of temporal gene expression data with mixtures of mixed effects models with a penalized likelihood · Bioinform. 2019
Bioinformatics and computational biology › gene expression analysis
model-based clustering
0.412019
Clustering of temporal gene expression data with mixtures of mixed effects models with a penalized likelihood · Bioinform. 2019
Bioinformatics and computational biology › gene expression analysis
time series clustering
0.412019
Clustering of temporal gene expression data with mixtures of mixed effects models with a penalized likelihood · Bioinform. 2019

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

penalized likelihood · 0.4expectation-maximization · 0.4entropy penalty · 0.4
YearPublicationVenuePosition
2019 Clustering of temporal gene expression data with mixtures of mixed effects models with a penalized likelihood
abstract
MOTIVATION: Clustering algorithms like K-Means and standard Gaussian mixture models (GMM) fail to account for the structure of variability of replicated data or repeated measures over time. Additionally, a priori cluster number assumptions add an additional complexity to the process. Current methods to optimize cluster labels and number can be inaccurate or computationally intensive for temporal gene expression data with this additional variability. RESULTS: An extension to a model-based clustering algorithm is proposed using mixtures of mixed effects polynomial regression models and the EM algorithm with an entropy penalized log-likelihood function (EPEM). The EPEM is used to cluster temporal gene expression data with this additional variability. The addition of random effects in our model decreased the misclassification error when compared to mixtures of fixed effects models or other methods such as K-Means and GMM. Applying our method to microarray data from a fracture healing study revealed distinct temporal patterns of gene expression. AVAILABILITY AND IMPLEMENTATION: https://github.com/darlenelu72/EPEM-GMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Darlene Lu, Yorghos Tripodis, Louis C. Gerstenfeld, Serkalem Demissie
Bioinform.1