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| 2. |
- Brandi, Maya, et al.
(författare)
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Multiscale modeling through MUSIC multi-simulation : Modeling a dendritic spine using MOOSE and NeuroRD
- 2011
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Ingår i: Front. Neuroinform. Conference Abstract. - : Frontiers Media SA.
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Konferensbidrag (refereegranskat)abstract
- The nervous system encompasses structure and phenomena at different spatial and temporal scales from molecule to behavior. In addition, different scales are described by different physical and mathematical formalisms. The dynamics of second messenger pathways can be formulated as stochastic reaction-diffusion systems [1] while the electrical dynamics of the neuronal membrane is often described by compartment models and the Hodgkin-Huxley formalism. In neuroscience, there is an increasing need and interest to study multi-scale phenomena where multiple scales and physical formalisms are covered by a single model. While there exists simulators/frameworks, such as GENESIS and MOOSE [3], which span such scales (kinetikit/HH-models), most software applications are specialized for a given domain. Here, we report about initial steps towards a framework for multi-scale modeling which builds on the concept of multi-simulations [2]. We aim to provide a standard API and communication framework allowing parallel simulators targeted at different scales and/or different physics to communicate on-line in a cluster environment. Specifically, we show prototype work on simulating the effect on receptor induced cascades on membrane excitability. Electrical properties of a compartment model is simulated in MOOSE, while receptor induced cascades are simulated in NeuroRD [4,7] . In a prototype system, the two simulators are connected using PyMOOSE [5] and JPype [6]. The two models with their different physical properties (membrane currents in MOOSE, molecular biophysics in NeuroRD), are joined into a single model system. We demonstrate the interaction of the numerical solvers of two simulators (MOOSE, NeuroRD) targeted at different spatiotemporal scales and different physics while solving a multi-scale problem. We analyze some of the problems that may arise in multi-scale multi-simulations and present requirements for a generic API for parallel solvers. This work represents initial steps towards a flexible modular framework for simulation of large-scale multi-scale multi-physics problems in neuroscience. References 1. Blackwell KT: An efficient stochastic diffusion algorithm for modeling second messengers in dendrites and spines. J Neurosci Meth 2006, 157: 142-153. 2. Djurfeldt M, Hjorth J, Eppler JM, Dudani N, Helias M, Potjans TC, Bhalla US, Diesmann M, Hellgren Kotaleski J, Ekeberg Ö: Run-Time Interoperability Between Neural Network Simulators Based on the MUSIC Framework. Neurinform 2010, 8: 43-60. 3. Dudani N, Ray S, George S, Bhalla US: Multiscale modeling and interoperability in MOOSE. Neuroscience 2009, 10(Suppl 1): 54. 4. Oliveira RF, Terrin A, Di Benedetto G, Cannon RC, Koh W, Kim M, Zaccolo M, Blacwell KT: The Role of Type 4 Phosphdiesterases in Generating Microdomains of cAMP: Large Scale Stochastic Simulations.
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| 3. |
- Djurfeldt, Mikael, et al.
(författare)
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Efficient generation of connectivity in neuronal networks from simulator-independent descriptions
- 2014
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Ingår i: Frontiers in Neuroinformatics. - : Frontiers Media SA. - 1662-5196. ; 8, s. 43-
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Tidskriftsartikel (refereegranskat)abstract
- Simulator-independent descriptions of connectivity in neuronal networks promise greater ease of model sharing, improved reproducibility of simulation results, and reduced programming effort for computational neuroscientists. However, until now, enabling the use of such descriptions in a given simulator in a computationally efficient way has entailed considerable work for simulator developers, which must be repeated for each new connectivity-generating library that is developed. We have developed a generic connection generator interface that provides a standard way to connect a connectivity-generating library to a simulator, such that one library can easily be replaced by another, according to the modeler's needs. We have used the connection generator interface to connect C++ and Python implementations of the previously described connection-set algebra to the NEST simulator. We also demonstrate how the simulator-independent modeling framework PyNN can transparently take advantage of this, passing a connection description through to the simulator layer for rapid processing in C++ where a simulator supports the connection generator interface and falling-back to slower iteration in Python otherwise. A set of benchmarks demonstrates the good performance of the interface.
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| 4. |
- Djurfeldt, Mikael, 1967-, et al.
(författare)
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Large-scale modeling - a tool for conquering the complexity of the brain
- 2008
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Ingår i: Frontiers in Neuroinformatics. - : Frontiers Media SA. - 1662-5196. ; 2, s. 1-4
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Tidskriftsartikel (refereegranskat)abstract
- Is there any hope of achieving a thorough understanding of higher functions such as perception, memory, thought and emotion or is the stunning complexity of the brain a barrier which will limit such efforts for the foreseeable future? In this perspective we discuss methods to handle complexity, approaches to model building, and point to detailed large-scale models as a new contribution to the toolbox of the computational neuroscientist. We elucidate some aspects which distinguishes large-scale models and some of the technological challenges which they entail.
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| 6. |
- Eklund, Anders, et al.
(författare)
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BROCCOLI : Software for fast fMRI analysis on many-core CPUs and GPUs
- 2014
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Ingår i: Frontiers in Neuroinformatics. - : Progressive Frontiers Press. - 1662-5196. ; 8:24
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Tidskriftsartikel (refereegranskat)abstract
- Analysis of functional magnetic resonance imaging (fMRI) data is becoming ever more computationally demanding as temporal and spatial resolutions improve, and large, publicly available data sets proliferate. Moreover, methodological improvements in the neuroimaging pipeline, such as non-linear spatial normalization, non-parametric permutation tests and Bayesian Markov Chain Monte Carlo approaches, can dramatically increase the computational burden. Despite these challenges, there do not yet exist any fMRI software packages which leverage inexpensive and powerful graphics processing units (GPUs) to perform these analyses. Here, we therefore present BROCCOLI, a free software package written in OpenCL (Open Computing Language) that can be used for parallel analysis of fMRI data on a large variety of hardware configurations. BROCCOLI has, for example, been tested with an Intel CPU, an Nvidia GPU, and an AMD GPU. These tests show that parallel processing of fMRI data can lead to significantly faster analysis pipelines. This speedup can be achieved on relatively standard hardware, but further, dramatic speed improvements require only a modest investment in GPU hardware. BROCCOLI (running on a GPU) can perform non-linear spatial normalization to a 1 mm3 brain template in 4–6 s, and run a second level permutation test with 10,000 permutations in about a minute. These non-parametric tests are generally more robust than their parametric counterparts, and can also enable more sophisticated analyses by estimating complicated null distributions. Additionally, BROCCOLI includes support for Bayesian first-level fMRI analysis using a Gibbs sampler. The new software is freely available under GNU GPL3 and can be downloaded from github (https://github.com/wanderine/BROCCOLI/).
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| 8. |
- Gu, Xuan, 1988-, et al.
(författare)
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Evaluation of Six Phase Encoding Based Susceptibility Distortion Correction Methods for Diffusion MRI
- 2019
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Ingår i: Frontiers in Neuroinformatics. - : Frontiers Media S.A.. - 1662-5196. ; 13
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Tidskriftsartikel (refereegranskat)abstract
- Purpose: Susceptibility distortions impact diffusion MRI data analysis and is typically corrected during preprocessing. Correction strategies involve three classes of methods: registration to a structural image, the use of a fieldmap, or the use of images acquired with opposing phase encoding directions. It has been demonstrated that phase encoding based methods outperform the other two classes, but unfortunately, the choice of which phase encoding based method to use is still an open question due to the absence of any systematic comparisons.Methods: In this paper we quantitatively evaluated six popular phase encoding based methods for correcting susceptibility distortions in diffusion MRI data. We employed a framework that allows for the simulation of realistic diffusion MRI data with susceptibility distortions. We evaluated the ability for methods to correct distortions by comparing the corrected data with the ground truth. Four diffusion tensor metrics (FA, MD, eigenvalues and eigenvectors) were calculated from the corrected data and compared with the ground truth. We also validated two popular indirect metrics using both simulated data and real data. The two indirect metrics are the difference between the corrected LR and AP data, and the FA standard deviation over the corrected LR, RL, AP, and PA data.Results: We found that DR-BUDDI and TOPUP offered the most accurate and robust correction compared to the other four methods using both direct and indirect evaluation metrics. EPIC and HySCO performed well in correcting b0 images but produced poor corrections for diffusion weighted volumes, and also they produced large errors for the four diffusion tensor metrics. We also demonstrate that the indirect metric (the difference between corrected LR and AP data) gives a different ordering of correction quality than the direct metric.Conclusion: We suggest researchers to use DR-BUDDI or TOPUP for susceptibility distortion correction. The two indirect metrics (the difference between corrected LR and AP data, and the FA standard deviation) should be interpreted together as a measure of distortion correction quality. The performance ranking of the various tools inferred from direct and indirect metrics differs slightly. However, across all tools, the results of direct and indirect metrics are highly correlated indicating that the analysis of indirect metrics may provide a good proxy of the performance of a correction tool if assessment using direct metrics is not feasible.
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| 9. |
- Gu, Xuan, 1988-, et al.
(författare)
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Using the wild bootstrap to quantify uncertainty in mean apparent propagator MRI
- 2019
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Ingår i: Frontiers in Neuroinformatics. - : Frontiers Media S.A.. - 1662-5196. ; 13
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Tidskriftsartikel (refereegranskat)abstract
- Purpose: Estimation of uncertainty of MAP-MRI metricsis an important topic, for several reasons. Bootstrap deriveduncertainty, such as the standard deviation, providesvaluable information, and can be incorporated in MAP-MRIstudies to provide more extensive insight.Methods: In this paper, the uncertainty of different MAPMRImetrics was quantified by estimating the empirical distributionsusing the wild bootstrap. We applied the wildbootstrap to both phantom data and human brain data, andobtain empirical distributions for theMAP-MRImetrics returnto-origin probability (RTOP), non-Gaussianity (NG) and propagatoranisotropy (PA).Results: We demonstrated the impact of diffusion acquisitionscheme (number of shells and number of measurementsper shell) on the uncertainty of MAP-MRI metrics.We demonstrated how the uncertainty of these metrics canbe used to improve group analyses, and to compare differentpreprocessing pipelines. We demonstrated that withuncertainty considered, the results for a group analysis canbe different.Conclusion: Bootstrap derived uncertain measures provideadditional information to the MAP-MRI derived metrics, andshould be incorporated in ongoing and future MAP-MRIstudies to provide more extensive insight.
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| 10. |
- Hansson, Kristin, et al.
(författare)
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RipleyGUI : software for analyzing spatial patterns in 3D cell distributions
- 2013
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Ingår i: Frontiers in Neuroinformatics. - : Frontiers Media SA. - 1662-5196. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- The true revolution in the age of digital neuroanatomy is the ability to extensively quantify anatomical structures and thus investigate structure-function relationships in great detail. To facilitate the quantification of neuronal cell patterns we have developed RipleyGUI, a MATLAB-based software that can be used to detect patterns in the 3D distribution of cells. RipleyGUI uses Ripley's K-function to analyze spatial distributions. In addition the software contains statistical tools to determine quantitative statistical differences, and tools for spatial transformations that are useful for analyzing non-stationary point patterns. The software has a graphical user interface making it easy to use without programming experience, and an extensive user manual explaining the basic concepts underlying the different statistical tools used to analyze spatial point patterns. The described analysis tool can be used for determining the spatial organization of neurons that is important for a detailed study of structure function relationships. For example, neocortex that can be subdivided into six layers based on cell density and cell types can also be analyzed in terms of organizational principles distinguishing the layers.
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