@misc{OberlaenderDercksenLangetal.2009, author = {Oberlaender, Marcel and Dercksen, Vincent J. and Lang, Stefan and Sakmann, Bert}, title = {3D mapping of synaptic connections within "in silico" microcircuits of full compartmental neurons in extended networks on the example of VPM axons projecting into S1 of rats.}, journal = {Conference Abstract, Neuroinformatics}, doi = {10.3389/conf.neuro.11.2009.08.092}, year = {2009}, language = {en} } @misc{OberlaenderBrunodeKocketal.2009, author = {Oberlaender, Marcel and Bruno, Randy M. and de Kock, Christiaan P. J. and Meyer, Hanno and Dercksen, Vincent J. and Sakmann, Bert}, title = {3D distribution and sub-cellular organization of thalamocortical VPM synapses for individual excitatory neuronal cell types in rat barrel cortex}, journal = {Conference Abstract No. 173.19/Y35, 39th Annual Meeting of the Society for Neuroscience (SfN)}, year = {2009}, language = {en} } @misc{OberlaenderDercksenBroseretal.2008, author = {Oberlaender, Marcel and Dercksen, Vincent J. and Broser, Philip J. and Bruno, Randy M. and Sakmann, Bert}, title = {NeuroMorph and NeuroCount: Automated tools for fast and objective acquisition of neuronal morphology for quantitative structural analysis}, journal = {Frontiers in Neuroinformatics. Conference Abstract: Neuroinformatics}, doi = {10.3389/conf.neuro.11.2008.01.065}, year = {2008}, language = {en} } @inproceedings{DercksenWeberGuentheretal.2009, author = {Dercksen, Vincent J. and Weber, Britta and G{\"u}nther, David and Oberlaender, Marcel and Prohaska, Steffen and Hege, Hans-Christian}, title = {Automatic alignment of stacks of filament data}, booktitle = {Proc. IEEE International Symposium on Biomedical Imaging}, publisher = {IEEE press}, address = {Boston, USA}, pages = {971 -- 974}, year = {2009}, language = {en} } @article{OberlaenderDercksenEggeretal.2009, author = {Oberlaender, Marcel and Dercksen, Vincent J. and Egger, Robert and Gensel, Maria and Sakmann, Bert and Hege, Hans-Christian}, title = {Automated three-dimensional detection and counting of neuron somata}, volume = {180}, journal = {Journal of Neuroscience Methods}, number = {1}, doi = {10.1016/j.jneumeth.2009.03.008}, pages = {147 -- 160}, year = {2009}, language = {en} } @misc{DercksenGenselKuss2009, author = {Dercksen, Vincent J. and Gensel, Maria and Kuß, Anja}, title = {Visual Accentuation of Spatial Relationships between Filamentous and Voluminous Surface Structures}, journal = {Conference Abstract, Eurographics / IEEE Symposium on Visualization}, year = {2009}, language = {en} } @article{EggerDercksenUdvaryetal.2014, author = {Egger, Robert and Dercksen, Vincent J. and Udvary, Daniel and Hege, Hans-Christian and Oberlaender, Marcel}, title = {Generation of dense statistical connectomes from sparse morphological data}, volume = {8}, journal = {Frontiers in Neuroanatomy}, number = {129}, doi = {10.3389/fnana.2014.00129}, year = {2014}, language = {en} } @incollection{PfisterKaynigBothaetal.2014, author = {Pfister, Hanspeter and Kaynig, Verena and Botha, Charl P. and Bruckner, Stefan and Dercksen, Vincent J. and Hege, Hans-Christian and Roerdink, Jos B.T.M.}, title = {Visualization in Connectomics}, booktitle = {Scientific Visualization - Uncertainty, Multifield, Biomedical, and Scalable Visualization}, editor = {Hansen, Charles D. and Chen, Min and Johnson, Christopher R. and Kaufman, Arie E. and Hagen, Hans}, publisher = {Springer}, isbn = {978-1-4471-6496-8}, arxiv = {http://arxiv.org/abs/1206.1428}, doi = {10.1007/978-1-4471-6497-5_21}, pages = {221 -- 245}, year = {2014}, abstract = {Connectomics is a branch of neuroscience that attempts to create a connectome, i.e., a complete map of the neuronal system and all connections between neuronal structures. This representation can be used to understand how functional brain states emerge from their underlying anatomical structures and how dysfunction and neuronal diseases arise. We review the current state-of-the-art of visualization and image processing techniques in the field of connectomics and describe a number of challenges. After a brief summary of the biological background and an overview of relevant imaging modalities, we review current techniques to extract connectivity information from image data at macro-, meso- and microscales. We also discuss data integration and neural network modeling, as well as the visualization, analysis and comparison of brain networks.}, language = {en} } @misc{EggerDercksenUdvaryetal.2014, author = {Egger, Robert and Dercksen, Vincent J. and Udvary, Daniel and Hege, Hans-Christian and Oberlaender, Marcel}, title = {Generation of dense statistical connectomes from sparse morphological data}, issn = {1438-0064}, doi = {10.3389/fnana.2014.00129}, url = {http://nbn-resolving.de/urn:nbn:de:0297-zib-53075}, year = {2014}, abstract = {Sensory-evoked signal flow, at cellular and network levels, is primarily determined by the synaptic wiring of the underlying neuronal circuitry. Measurements of synaptic innervation, connection probabilities and sub-cellular organization of synaptic inputs are thus among the most active fields of research in contemporary neuroscience. Methods to measure these quantities range from electrophysiological recordings over reconstructions of dendrite-axon overlap at light-microscopic levels to dense circuit reconstructions of small volumes at electron-microscopic resolution. However, quantitative and complete measurements at subcellular resolution and mesoscopic scales to obtain all local and long-range synaptic in/outputs for any neuron within an entire brain region are beyond present methodological limits. Here, we present a novel concept, implemented within an interactive software environment called NeuroNet, which allows (i) integration of sparsely sampled (sub)cellular morphological data into an accurate anatomical reference frame of the brain region(s) of interest, (ii) up-scaling to generate an average dense model of the neuronal circuitry within the respective brain region(s) and (iii) statistical measurements of synaptic innervation between all neurons within the model. We illustrate our approach by generating a dense average model of the entire rat vibrissal cortex, providing the required anatomical data, and illustrate how to measure synaptic innervation statistically. Comparing our results with data from paired recordings in vitro and in vivo, as well as with reconstructions of synaptic contact sites at light- and electron-microscopic levels, we find that our in silico measurements are in line with previous results.}, language = {en} }