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Stefan Roepcke

dblp:81/1759 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2008
0000-0003-1271-1590ORCID · corroborated

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › network bioinformatics › biological network analysis
functional module identification
0.112008
Inferring differentiation pathways from gene expression · ISMB 2008
Bioinformatics and computational biology
gene expression analysis
0.112008
Inferring differentiation pathways from gene expression · ISMB 2008
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112005
MACAT - microarray chromosome analysis tool · Bioinform. 2005

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

unsupervised learning · 0.1mixture of trees · 0.1statistical analysis · 0.1
YearPublicationVenuePosition
2008 Inferring differentiation pathways from gene expression
abstract
MOTIVATION: The regulation of proliferation and differentiation of embryonic and adult stem cells into mature cells is central to developmental biology. Gene expression measured in distinguishable developmental stages helps to elucidate underlying molecular processes. In previous work we showed that functional gene modules, which act distinctly in the course of development, can be represented by a mixture of trees. In general, the similarities in the gene expression programs of cell populations reflect the similarities in the differentiation path. RESULTS: We propose a novel model for gene expression profiles and an unsupervised learning method to estimate developmental similarity and infer differentiation pathways. We assess the performance of our model on simulated data and compare it with favorable results to related methods. We also infer differentiation pathways and predict functional modules in gene expression data of lymphoid development. CONCLUSIONS: We demonstrate for the first time how, in principal, the incorporation of structural knowledge about the dependence structure helps to reveal differentiation pathways and potentially relevant functional gene modules from microarray datasets. Our method applies in any area of developmental biology where it is possible to obtain cells of distinguishable differentiation stages. AVAILABILITY: The implementation of our method (GPL license), data and additional results are available at http://algorithmics.molgen.mpg.de/Supplements/InfDif/. SUPPLEMENTARY INFORMATION: Supplementary data is available at Bioinformatics online.
Ivan G. Costa, Stefan Roepcke, Christoph Hafemeister, Alexander Schliep
ISMB2
2005 MACAT - microarray chromosome analysis tool
abstract
UNLABELLED: By linking differential gene expression to the chromosomal localization of genes, one can investigate microarray data for characteristic patterns of expression phenomena involving sizeable parts of specific chromosomes. We have implemented a statistical approach for identifying significantly differentially expressed chromosome regions. We demonstrate the applicability of the approach on a publicly available data set on acute lymphocytic leukemia. AVAILABILITY: The R-package MACAT can be obtained from http://www.compdiag.molgen.mpg.de/software/macat.shtml SUPPLEMENTARY INFORMATION: http://www.compdiag.molgen.mpg.de/software/macat.shtml.
Joern Toedling, Sebastian Schmeier, Matthias Heinig, Benjamin Georgi, Stefan Roepcke
Bioinform.5