Frontiers in Neuroinformatics Journal Impact Factor & Information

Publisher: Frontiers Research Foundation, Frontiers

Journal description

Current impact factor: 3.26

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2014 Impact Factor 3.261

Additional details

5-year impact 0.00
Cited half-life 3.80
Immediacy index 0.71
Eigenfactor 0.00
Article influence 0.00
ISSN 1662-5196
OCLC 250621701
Material type Document, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details


  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author can archive a post-print version
  • Conditions
    • On open access repositories
    • Authors retain copyright
    • Creative Commons Attribution License
    • Published source must be acknowledged
    • Publisher's version/PDF may be used
    • Set statement to accompany [This Document is Protected by copyright and was first published by Frontiers. All rights reserved. it is reproduced with permission.]
    • Articles are placed in PubMed Central immediately on behalf of authors.
    • All titles are open access journals
    • Publisher last contacted on 16/07/2015
  • Classification
    ​ green

Publications in this journal

  • Frontiers in Neuroinformatics 09/2015; 9. DOI:10.3389/fninf.2015.00023
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    ABSTRACT: Contemporary simulators for networks of point and few-compartment model neurons come with a plethora of ready-to-use neuron and synapse models and support complex network topologies. Recent technological advancements have broadened the spectrum of application further to the efficient simulation of brain-scale networks on supercomputers. In distributed network simulations the amount of spike data that accrues per millisecond and process is typically low, such that a common optimization strategy is to communicate spikes at relatively long intervals, where the upper limit is given by the shortest synaptic transmission delay in the network. This approach is well-suited for simulations that employ only chemical synapses but it has so far impeded the incorporation of gap-junction models, which require instantaneous neuronal interactions. Here, we present a numerical algorithm based on a waveform-relaxation technique which allows for network simulations with gap junctions in a way that is compatible with the delayed communication strategy. Using a reference implementation in the NEST simulator, we demonstrate that the algorithm and the required data structures can be smoothly integrated with existing code such that they complement the infrastructure for spiking connections. To show that the unified framework for gap-junction and spiking interactions achieves high performance and delivers high accuracy in the presence of gap junctions, we present benchmarks for workstations, clusters, and supercomputers. Finally, we discuss limitations of the novel technology.
    Frontiers in Neuroinformatics 09/2015; 9. DOI:10.3389/fninf.2015.00022
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    ABSTRACT: Many modern neural simulators focus on the simulation of networks of spiking neurons on parallel hardware. Another important framework in computational neuroscience, rate-coded neural networks, is mostly difficult or impossible to implement using these simulators. We present here the ANNarchy (Artificial Neural Networks architect) neural simulator, which allows to easily define and simulate rate-coded and spiking networks, as well as combinations of both. The interface in Python has been designed to be close to the PyNN interface, while the definition of neuron and synapse models can be specified using an equation-oriented mathematical description similar to the Brian neural simulator. This information is used to generate C++ code that will efficiently perform the simulation on the chosen parallel hardware (multi-core system or graphical processing unit). Several numerical methods are available to transform ordinary differential equations into an efficient C++code. We compare the parallel performance of the simulator to existing solutions.
    Frontiers in Neuroinformatics 08/2015; 9:19. DOI:10.3389/fninf.2015.00019
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    ABSTRACT: Neurons come in a wide variety of shapes and sizes. In a quest to understand this neuronal diversity, researchers have three-dimensionally traced tens of thousands of neurons; many of these tracings are freely available through online repositories like NeuroMorpho.Org and ModelDB. Tracings can be visualized on the computer screen, used for statistical analysis of the properties of different cell types, used to simulate neuronal behavior, and more. We introduce the use of 3D printing as a technique for visualizing traced morphologies. Our method for generating printable versions of a cell or group of cells is to expand dendrite and axon diameters and then to transform the tracing into a 3D object with a neuronal surface generating algorithm like Constructive Tessellated Neuronal Geometry (CTNG). We show that 3D printed cells can be readily examined, manipulated, and compared with other neurons to gain insight into both the biology and the reconstruction process. We share our printable models in a new database, 3DModelDB, and encourage others to do the same with cells that they generate using our code or other methods. To provide additional context, 3DModelDB provides a simulatable version of each cell, links to papers that use or describe it, and links to associated entries in other databases.
    Frontiers in Neuroinformatics 06/2015; 9:18. DOI:10.3389/fninf.2015.00018
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    ABSTRACT: Most of the software platforms for cellular electrophysiology are limited in terms of flexibility, hardware support, ease of use, or re-configuration and adaptation for non-expert users. Moreover, advanced experimental protocols requiring real-time closed-loop operation to investigate excitability, plasticity, dynamics, are largely inaccessible to users without moderate to substantial computer proficiency. Here we present an approach based on MATLAB/Simulink, exploiting the benefits of LEGO-like visual programming and configuration, combined to a small, but easily extendible library of functional software components. We provide and validate several examples, implementing conventional and more sophisticated experimental protocols such as dynamic-clamp or the combined use of intracellular and extracellular methods, involving closed-loop real-time control. The functionality of each of these examples is demonstrated with relevant experiments. These can be used as a starting point to create and support a larger variety of electrophysiological tools and methods, hopefully extending the range of default techniques and protocols currently employed in experimental labs across the world.
    Frontiers in Neuroinformatics 06/2015; 9:17. DOI:10.3389/fninf.2015.00017
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    Frontiers in Neuroinformatics 06/2015; 9:15. DOI:10.3389/fninf.2015.00015
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    ABSTRACT: [This corrects the article on p. 71 in vol. 8, PMID: 25206330.].
    Frontiers in Neuroinformatics 06/2015; 9. DOI:10.3389/fninf.2015.00014
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    ABSTRACT: Spiking neuron models can accurately predict the response of neurons to somatically injected currents if the model parameters are carefully tuned. Predicting the response of in-vivo neurons responding to natural stimuli presents a far more challenging modeling problem. In this study, an algorithm is presented for parameter estimation of spiking neuron models. The algorithm is a hybrid evolutionary algorithm which uses a spike train metric as a fitness function. We apply this to parameter discovery in modeling two experimental data sets with spiking neurons; in-vitro current injection responses from a regular spiking pyramidal neuron are modeled using spiking neurons and in-vivo extracellular auditory data is modeled using a two stage model consisting of a stimulus filter and spiking neuron model.
    Frontiers in Neuroinformatics 04/2015; 9:10. DOI:10.3389/fninf.2015.00010
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    ABSTRACT: Different non-invasive neuroimaging modalities and multi-level analysis of human connectomics datasets yield a great amount of heterogeneous data which are hard to integrate into an unified representation. Biomedical ontologies can provide a suitable integrative framework for domain knowledge as well as a tool to facilitate information retrieval, data sharing and data comparisons across scales, modalities and species. Especially, it is urgently needed to fill the gap between neurobiology and in vivo human connectomics in order to better take into account the reality highlighted in Magnetic Resonance Imaging (MRI) and relate it to existing brain knowledge. The aim of this study was to create a neuroanatomical ontology, called "Human Connectomics Ontology" (HCO), in order to represent macroscopic gray matter regions connected with fiber bundles assessed by diffusion tractography and to annotate MRI connectomics datasets acquired in the living human brain. First a neuroanatomical "view" called NEURO-DL-FMA was extracted from the reference ontology Foundational Model of Anatomy (FMA) in order to construct a gross anatomy ontology of the brain. HCO extends NEURO-DL-FMA by introducing entities (such as "MR_Node" and "MR_Route") and object properties (such as "tracto_connects") pertaining to MR connectivity. The Web Ontology Language Description Logics (OWL DL) formalism was used in order to enable reasoning with common reasoning engines. Moreover, an experimental work was achieved in order to demonstrate how the HCO could be effectively used to address complex queries concerning in vivo MRI connectomics datasets. Indeed, neuroimaging datasets of five healthy subjects were annotated with terms of the HCO and a multi-level analysis of the connectivity patterns assessed by diffusion tractography of the right medial Brodmann Area 6 was achieved using a set of queries. This approach can facilitate comparison of data across scales, modalities and species.
    Frontiers in Neuroinformatics 04/2015; 9:9. DOI:10.3389/fninf.2015.00009
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    Frontiers in Neuroinformatics 03/2015; 9:5. DOI:10.3389/fninf.2015.00005
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    ABSTRACT: This paper presents a system for declaratively transforming medical subjects' data into a common data model representation. Our work is part of the "GAAIN" project on Alzheimer's disease data federation across multiple data providers. We present a general purpose data transformation system that we have developed by leveraging the existing state-of-the-art in data integration and query rewriting. In this work we have further extended the current technology with new formalisms that facilitate expressing a broader range of data transformation tasks, plus new execution methodologies to ensure efficient data transformation for disease datasets.
    Frontiers in Neuroinformatics 02/2015; 9:1. DOI:10.3389/fninf.2015.00001