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Jan U. Lohmann

dblp:312/0404 · DBLP profile ↗
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3ranked-venue papers
0as first author
0since 2021 · last 2020
0000-0003-3667-187XORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 3

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 regulation › regulatory element discovery
cis-regulatory module prediction
0.112009
KIRMES: kernel-based identification of regulatory modules in euchromatic sequences · Bioinform. 2009
Bioinformatics and computational biology › gene regulation › gene regulatory network
regulatory module identification
0.112009
KIRMES: kernel-based identification of regulatory modules in euchromatic sequences · Bioinform. 2009
Bioinformatics and computational biology › gene regulation
transcription factor binding site prediction
0.112009
KIRMES: kernel-based identification of regulatory modules in euchromatic sequences · Bioinform. 2009

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

support vector machine · 0.1kernel methods · 0.1gibbs sampling · 0.1
YearPublicationVenuePosition
2020 Mathematical modeling of plant cell fate transitions controlled by hormonal signals
abstract
Coordination of fate transition and cell division is crucial to maintain the plant architecture and to achieve efficient production of plant organs. In this paper, we analysed the stem cell dynamics at the shoot apical meristem (SAM) that is one of the plant stem cells locations. We designed a mathematical model to elucidate the impact of hormonal signaling on the fate transition rates between different zones corresponding to slowly dividing stem cells and fast dividing transit amplifying cells. The model is based on a simplified two-dimensional disc geometry of the SAM and accounts for a continuous displacement towards the periphery of cells produced in the central zone. Coupling growth and hormonal signaling results in a nonlinear system of reaction-diffusion equations on a growing domain with the growth rate depending on the model components. The model is tested by simulating perturbations in the level of key transcription factors that maintain SAM homeostasis. The model provides new insights on how the transcription factor HECATE is integrated in the regulatory network that governs stem cell differentiation.
Filip Z. Klawe, Thomas Stiehl, Peter Bastian, Christophe Gaillochet, Jan U. Lohmann, Anna K. Marciniak-Czochra
PLoS Comput. Biol.5
2009 KIRMES: kernel-based identification of regulatory modules in euchromatic sequences
abstract
MOTIVATION: Understanding transcriptional regulation is one of the main challenges in computational biology. An important problem is the identification of transcription factor (TF) binding sites in promoter regions of potential TF target genes. It is typically approached by position weight matrix-based motif identification algorithms using Gibbs sampling, or heuristics to extend seed oligos. Such algorithms succeed in identifying single, relatively well-conserved binding sites, but tend to fail when it comes to the identification of combinations of several degenerate binding sites, as those often found in cis-regulatory modules. RESULTS: We propose a new algorithm that combines the benefits of existing motif finding with the ones of support vector machines (SVMs) to find degenerate motifs in order to improve the modeling of regulatory modules. In experiments on microarray data from Arabidopsis thaliana, we were able to show that the newly developed strategy significantly improves the recognition of TF targets. AVAILABILITY: The python source code (open source-licensed under GPL), the data for the experiments and a Galaxy-based web service are available at http://www.fml.mpg.de/raetsch/suppl/kirmes/.
Sebastian J. Schultheiß, Wolfgang Busch, Jan U. Lohmann, Oliver Kohlbacher, Gunnar Rätsch
Bioinform.3
2009 KIRMES: kernel-based identification of regulatory modules in euchromatic sequences
Sebastian J. Schultheiß, Wolfgang Busch, Jan U. Lohmann, Oliver Kohlbacher, Gunnar Rätsch
BMC Bioinform.3