Gemma Taverni, Diederik Paul Moeys, F. Voigt, Chenghan Li, C. Cavaco, V. Motsnyi, Stewart Berry, Pia Sipila, D. S. S. Bello, F. Helmchen, T. Delbrück
{"title":"In-vivo imaging of neural activity with dynamic vision sensors","authors":"Gemma Taverni, Diederik Paul Moeys, F. Voigt, Chenghan Li, C. Cavaco, V. Motsnyi, Stewart Berry, Pia Sipila, D. S. S. Bello, F. Helmchen, T. Delbrück","doi":"10.1109/BIOCAS.2017.8325076","DOIUrl":null,"url":null,"abstract":"Optical recording of neural activity using calcium or voltage indicators requires cameras capable of detecting small temporal contrast in light intensity with sample rates of 10 Hz to 1 kHz. Large pixel scientific CMOS image sensors (sCMOS) are typically used due to their high resolution, high frame rate, and low noise. However, using such sensors for long-term recording is challenging due to their high data rates of up to 1 Gb/s. Here we studied the use of dynamic vision sensor (DVS) event cameras for neural recording. DVS have high dynamic range and a sparse asynchronous output consisting of brightness change events. Using DVS for neural recording could avoid transferring and storing redundant information. We compared the use of a Hamamatsu Orca V2 sCMOS with two advanced DVS sensors (a higher temporal contrast sensitivity 188×180 pixel SDAVIS and a 346×260 pixel higher light sensitivity back-side-illuminated BSIDAVIS) for neural activity recordings with fluorescent calcium indicators both in brain slices and awake mice. The DVS activity responds to the fast dynamics of neural activity, indicating that a sensor combining SDAVIS and BSIDAVIS technologies would be beneficial for long-term in-vivo neural recording using calcium indicators as well as potentially faster voltage indicators.","PeriodicalId":361477,"journal":{"name":"2017 IEEE Biomedical Circuits and Systems Conference (BioCAS)","volume":"30 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2017 IEEE Biomedical Circuits and Systems Conference (BioCAS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BIOCAS.2017.8325076","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
Abstract
Optical recording of neural activity using calcium or voltage indicators requires cameras capable of detecting small temporal contrast in light intensity with sample rates of 10 Hz to 1 kHz. Large pixel scientific CMOS image sensors (sCMOS) are typically used due to their high resolution, high frame rate, and low noise. However, using such sensors for long-term recording is challenging due to their high data rates of up to 1 Gb/s. Here we studied the use of dynamic vision sensor (DVS) event cameras for neural recording. DVS have high dynamic range and a sparse asynchronous output consisting of brightness change events. Using DVS for neural recording could avoid transferring and storing redundant information. We compared the use of a Hamamatsu Orca V2 sCMOS with two advanced DVS sensors (a higher temporal contrast sensitivity 188×180 pixel SDAVIS and a 346×260 pixel higher light sensitivity back-side-illuminated BSIDAVIS) for neural activity recordings with fluorescent calcium indicators both in brain slices and awake mice. The DVS activity responds to the fast dynamics of neural activity, indicating that a sensor combining SDAVIS and BSIDAVIS technologies would be beneficial for long-term in-vivo neural recording using calcium indicators as well as potentially faster voltage indicators.