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Padraig Gleeson
University College London
p.gleeson@ucl.ac.uk

Journal articles

2007
 
PMID 
Robert C Cannon, Marc-Oliver Gewaltig, Padraig Gleeson, Upinder S Bhalla, Hugo Cornelis, Michael L Hines, Fredrick W Howell, Eilif Muller, Joel R Stiles, Stefan Wils, Erik De Schutter (2007)  Interoperability of neuroscience modeling software: current status and future directions.   Neuroinformatics 5: 2. 127-138  
Abstract: Neuroscience increasingly uses computational models to assist in the exploration and interpretation of complex phenomena. As a result, considerable effort is invested in the development of software tools and technologies for numerical simulations and for the creation and publication of models. The diversity of related tools leads to the duplication of effort and hinders model reuse. Development practices and technologies that support interoperability between software systems therefore play an important role in making the modeling process more efficient and in ensuring that published models can be reliably and easily reused. Various forms of interoperability are possible including the development of portable model description standards, the adoption of common simulation languages or the use of standardized middleware. Each of these approaches finds applications within the broad range of current modeling activity. However more effort is required in many areas to enable new scientific questions to be addressed. Here we present the conclusions of the "Neuro-IT Interoperability of Simulators" workshop, held at the 11th computational neuroscience meeting in Edinburgh ( July 19-20 2006; http://www.cnsorg.org ). We assess the current state of interoperability of neural simulation software and explore the future directions that will enable the field to advance.
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PMID 
Sharon Crook, Padraig Gleeson, Fred Howell, Joseph Svitak, R Angus Silver (2007)  MorphML: level 1 of the NeuroML standards for neuronal morphology data and model specification.   Neuroinformatics 5: 2. 96-104  
Abstract: Quantitative neuroanatomical data are important for the study of many areas of neuroscience, and the complexity of problems associated with neuronal structure requires that research from multiple groups across many disciplines be combined. However, existing neuron-tracing systems, simulation environments, and tools for the visualization and analysis of neuronal morphology data use a variety of data formats, making it difficult to exchange data in a readily usable way. The NeuroML project was initiated to address these issues, and here we describe an extensible markup language standard, MorphML, which defines a common data format for neuronal morphology data and associated metadata to facilitate data and model exchange, database creation, model publication, and data archiving. We describe the elements of the standard in detail and outline the mappings between this format and those used by a number of popular applications for reconstruction, simulation, and visualization of neuronal morphology.
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DOI   
PMID 
Padraig Gleeson, Volker Steuber, R Angus Silver (2007)  neuroConstruct: a tool for modeling networks of neurons in 3D space.   Neuron 54: 2. 219-235 Apr  
Abstract: Conductance-based neuronal network models can help us understand how synaptic and cellular mechanisms underlie brain function. However, these complex models are difficult to develop and are inaccessible to most neuroscientists. Moreover, even the most biologically realistic network models disregard many 3D anatomical features of the brain. Here, we describe a new software application, neuroConstruct, that facilitates the creation, visualization, and analysis of networks of multicompartmental neurons in 3D space. A graphical user interface allows model generation and modification without programming. Models within neuroConstruct are based on new simulator-independent NeuroML standards, allowing automatic generation of code for NEURON or GENESIS simulators. neuroConstruct was tested by reproducing published models and its simulator independence verified by comparing the same model on two simulators. We show how more anatomically realistic network models can be created and their properties compared with experimental measurements by extending a published 1D cerebellar granule cell layer model to 3D.
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