William Meiniel, P. Spinicelli, E. Angelini, A. Fragola, V. Loriette, F. Orieux, E. Sepúlveda, J. Olivo-Marin
{"title":"Reducing data acquisition for fast Structured Illumination Microscopy using Compressed Sensing","authors":"William Meiniel, P. Spinicelli, E. Angelini, A. Fragola, V. Loriette, F. Orieux, E. Sepúlveda, J. Olivo-Marin","doi":"10.1109/ISBI.2017.7950461","DOIUrl":null,"url":null,"abstract":"In this work, we introduce an original strategy to apply the Compressed Sensing (CS) framework to a super-resolution Structured Illumination Microscopy (SIM) technique. We first define a framework for direct domain CS, that exploits the sparsity of fluorescence microscopy images in the Fourier domain. We then propose an application of this method to a fast 4-images SIM technique, which allows to reconstruct super-resolved fluorescence microscopy images using only 25% of the camera pixels for each acquisition.","PeriodicalId":6547,"journal":{"name":"2017 IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017)","volume":"33 1","pages":"32-35"},"PeriodicalIF":0.0000,"publicationDate":"2017-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2017 IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ISBI.2017.7950461","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10
Abstract
In this work, we introduce an original strategy to apply the Compressed Sensing (CS) framework to a super-resolution Structured Illumination Microscopy (SIM) technique. We first define a framework for direct domain CS, that exploits the sparsity of fluorescence microscopy images in the Fourier domain. We then propose an application of this method to a fast 4-images SIM technique, which allows to reconstruct super-resolved fluorescence microscopy images using only 25% of the camera pixels for each acquisition.