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Inferring signalling networks from longitudinal data using sampling based approaches in the R-package 'ddepn'
Christian Bender1, Silvia vd Heyde, Frauke Henjes
1German Cancer Research Center (DKFZ), Division of Molecular Genome Analysis, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany. c.bender@dkfz-heidelberg.de
This study introduces the R-package "ddepn" for biological network inference from longitudinal data. It enables hypothesis generation for cancer research by reconstructing signaling networks with novel methods.
Area of Science:
- Systems Biology
- Computational Biology
- Bioinformatics
Background:
- Network inference from high-throughput data is crucial for understanding biological systems.
- Signaling networks of cancer-related proteins are key to identifying pathways influencing tumor development.
- Cancer cell lines provide models for time-resolved study of drug treatment responses.
Purpose of the Study:
- To develop and present a computational approach for network reconstruction from longitudinal data.
- To enable hypothesis generation regarding potential interference points in biological networks.
Main Methods:
- Implementation of a novel network reconstruction approach in the R-package 'ddepn'.
- Utilizing a Markov Chain Monte Carlo method for sampling network structures with activation and inhibition edges.
- Extending a prior model to penalize deviations from a reference network and incorporating scale-free network properties.
Main Results:
- The R-package 'ddepn' facilitates network inference from longitudinal high-throughput data.
- Novel methods allow for the reconstruction of signaling networks with directed edges (activation/inhibition).
- The package supports different prior models, including those learning scale-free network properties.
Conclusions:
- The 'ddepn' R-package is available on R-Forge and CRAN for convenient use.
- It enables network inference from longitudinal data using advanced sampling-based algorithms.
- This tool aids in the analysis of biological networks, particularly in cancer research.
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