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

Marc Daniel Haunschild

dblp:00/599 · DBLP profile ↗
← Back
1ranked-venue papers
1as first author
0since 2021 · last 2005
—ORCID · none

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%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
Distributed systems · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › systems biology › biochemical modeling
biochemical network modeling
0.112005
Investigating the dynamic behavior of biochemical networks using model families · Bioinform. 2005
Bioinformatics and computational biology › systems biology › metabolic network analysis
elementary flux modes
0.112005
Investigating the dynamic behavior of biochemical networks using model families · Bioinform. 2005
Distributed systems
grid computing
0.012005
Investigating the dynamic behavior of biochemical networks using model families · Bioinform. 2005

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

spline interpolation · 0.1combinatorial model specification · 0.1automatic differentiation · 0.1
YearPublicationVenuePosition
2005 Investigating the dynamic behavior of biochemical networks using model families
abstract
MOTIVATION: Supporting the evolutionary modeling process of dynamic biochemical networks based on sampled in vivo data requires more than just simulation. In the course of the modeling process, the modeler is typically concerned not only with a single model but also with sequences, alternatives and structural variants of models. Powerful automatic methods are then required to assist the modeler in the organization and the evaluation of alternative models. Moreover, the structure and peculiarities of the data require dedicated tool support. SUMMARY: To support all stages of an evolutionary modeling process, a new general formalism for the combinatorial specification of large model families is introduced. It allows for automatic navigation in the space of models and excludes biologically meaningless models on the basis of elementary flux mode analysis. An incremental usage of the measured data is supported by using splined data instead of state variables. With MMT2, a versatile tool has been developed as a computational engine intended to be built into a tool chain. Using automatic code generation, automatic differentiation for sensitivity analysis and grid computing technology, a high performance computing environment is achieved. MMT2 supplies XML model specification and several software interfaces. The performance of MMT2 is illustrated by several examples from ongoing research projects. AVAILABILITY: http://www.simtec.mb.uni-siegen.de/ CONTACT: [email protected].
Marc Daniel Haunschild, Bernd Freisleben, Ralf Takors, Wolfgang Wiechert
Bioinform.1