S. Breit

dblp:98/6847 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2004
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2

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
0.012004
mdclust-exploratory microarray analysis by multidimensional clustering · Bioinform. 2004
Bioinformatics and computational biology › gene expression analysis › gene expression clustering
microarray data clustering
0.012004
mdclust-exploratory microarray analysis by multidimensional clustering · Bioinform. 2004
Bioinformatics and computational biology › statistical genetics › genotype-phenotype association
gene-phenotype association
0.012004
mdclust-exploratory microarray analysis by multidimensional clustering · Bioinform. 2004

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

two-means clustering · 0.0score-based gene selection · 0.0discriminant analysis · 0.0
YearPublicationVenuePosition
2004 mdclust-exploratory microarray analysis by multidimensional clustering
abstract
Abstract Motivation: Unsupervised clustering of microarray data may detect potentially important, but not obvious characteristics of samples, for instance subgroups of diagnoses with distinct gene profiles or systematic errors in experimentation. Results: Multidimensional clustering (mdclust) is a method, which identifies sets of sample clusters and associated genes. It applies iteratively two-means clustering and score-based gene selection. For any phenotype variable best matching sets of clusters can be selected. This provides a method to identify gene–phenotype associations, suited even for settings with a large number of phenotype variables. An optional model based discriminant step may reduce further the number of selected genes. Availability: R-code and supplemental information available from http://martin-dugas.de/mdclust/ Supplementary information: http://martin-dugas.de/mdclust/
Martin Dugas, Sylvia Merk, S. Breit, P. Dirschedl
Bioinform.3
2003 Bioinformatics for Medical Diagnostics: Assessment of Microarray Data in the Context of Clinical Databases
Martin Dugas, Sylvia Merk, S. Breit, Claudia Schoch, Torsten Haferlach, Stefan Kääb
AMIA3