MEA-ToolBox: an Open Source Toolbox for Standardized Analysis of Multi-Electrode Array Data

被引:0
作者
Michel Hu
Monica Frega
Else A. Tolner
A. M. J. M. van den Maagdenberg
J. P. Frimat
Joost le Feber
机构
[1] Leiden University Medical Centre,Department of Human Genetics
[2] Leiden University Medical Centre,Department of Neurology
[3] University of Twente,Department of Clinical Neurophysiology
来源
Neuroinformatics | 2022年 / 20卷
关键词
Electrophysiology; Data visualization; Burst analysis; Multi-electrode array; Neuron; Spike analysis;
D O I
暂无
中图分类号
学科分类号
摘要
Functional assessment of in vitro neuronal networks—of relevance for disease modelling and drug testing—can be performed using multi-electrode array (MEA) technology. However, the handling and processing of the large amount of data typically generated in MEA experiments remains a huge hurdle for researchers. Various software packages have been developed to tackle this issue, but to date, most are either not accessible through the links provided by the authors or only tackle parts of the analysis. Here, we present ‘‘MEA-ToolBox’’, a free open-source general MEA analytical toolbox that uses a variety of literature-based algorithms to process the data, detect spikes from raw recordings, and extract information at both the single-channel and array-wide network level. MEA-ToolBox extracts information about spike trains, burst-related analysis and connectivity metrics without the need of manual intervention. MEA-ToolBox is tailored for comparing different sets of measurements and will analyze data from multiple recorded files placed in the same folder sequentially, thus considerably streamlining the analysis pipeline. MEA-ToolBox is available with a graphic user interface (GUI) thus eliminating the need for any coding expertise while offering functionality to inspect, explore and post-process the data. As proof-of-concept, MEA-ToolBox was tested on earlier-published MEA recordings from neuronal networks derived from human induced pluripotent stem cells (hiPSCs) obtained from healthy subjects and patients with neurodevelopmental disorders. Neuronal networks derived from patient’s hiPSCs showed a clear phenotype compared to those from healthy subjects, demonstrating that the toolbox could extract useful parameters and assess differences between normal and diseased profiles.
引用
收藏
页码:1077 / 1092
页数:15
相关论文
共 79 条
[1]  
Bateup HS(2013)Excitatory/Inhibitory Synaptic Imbalance Leads to Hippocampal Hyperexcitability in Mouse Models of Tuberous Sclerosis Neuron 78 510-522
[2]  
Becchetti A(2012)Exact distinction of excitatory and inhibitory neurons in neural networks: A study with GFP-GAD67 neurons optically and electrophysiologically recognized on multielectrode arrays Front. Neural Circuits 6 1-11
[3]  
Bologna LL(2010)Investigating neuronal activity by SPYCODE multi-channel data analyzer Neural Networks 23 685-697
[4]  
Bradley JA(2018)In vitro screening for seizure liability using microelectrode array technology Toxicological Sciences 163 240-253
[5]  
Luithardt HH(2012)Clustered burst firing in FMR1 premutation hippocampal neurons: Amelioration with allopregnanolone Human Molecular Genetics 21 2923-2935
[6]  
Metea MR(2016)A comparison of computational methods for detecting bursts in neuronal spike trains and their application to human stem cell-derived neuronal networks Journal of Neurophysiology 116 306-321
[7]  
Strock CJ(2008)BSMART: A Matlab/C toolbox for analysis of multichannel neural time series Neural Networks 21 1094-1104
[8]  
Cao Z(2020)MEAnalyzer – a Spike Train Analysis Tool for Multi Electrode Arrays Neuroinformatics 18 163-179
[9]  
Cotterill E(2019)Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling Nature Communications 10 1-15
[10]  
Charlesworth P(2018)meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays PLoS Computational Biology 14 1-20