Smith CS, Slotman JA, Schermelleh L, et al. Structured illumination microscopy with noise-controlled image reconstructions. Nature Methods. 2021;18(7):821-828.Super-resolution structured illumination microscopy (SIM) has become a widely used method for biological imaging. Standard reconstruction algorithms, however, are prone to generate noise-specific artifacts that limit their applicability for lower signal-to-noise data. Here we present a physically realistic noise model that explains the structured noise artifact, which we then use to motivate new complementary reconstruction approaches. True-Wiener-filtered SIM optimizes contrast given the available signal-to-noise ratio, and flat-noise SIM fully overcomes the structured noise artifact...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...
This version contains the updated results of the article " Deep-learning based denoising and reconst...
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A strai...
Super-resolution structured illumination microscopy (SIM) has become a widely used method for biolog...
Super-resolution structured illumination microscopy (SIM) has become a widely used method for biolog...
Structured illumination microscopy (SIM) is widely applied due to its high temporal and spatial reso...
The impact of the different reconstruction parameters in super-resolution structured illumination mi...
Structured illumination microscopy (SIM) is one of the most widely applied super-resolution microsco...
Of all 3D-super resolution techniques, structured illumination microscopy (SIM) provides the best co...
This thesis investigates ways for assessing the practical lateral resolution performance of imaging ...
Structured illumination microscopy (SIM) has become an important technique for optical super-resolut...
Three-dimensional fluorescence imaging is an essential tool in biology, used for everything from lon...
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A strai...
Heintzmann R, Huser T. Super-Resolution Structured Illumination Microscopy. CHEMICAL REVIEWS. 2017;1...
Structured illumination microscopy (SIM) is a very important super-resolution microscopy technique, ...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...
This version contains the updated results of the article " Deep-learning based denoising and reconst...
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A strai...
Super-resolution structured illumination microscopy (SIM) has become a widely used method for biolog...
Super-resolution structured illumination microscopy (SIM) has become a widely used method for biolog...
Structured illumination microscopy (SIM) is widely applied due to its high temporal and spatial reso...
The impact of the different reconstruction parameters in super-resolution structured illumination mi...
Structured illumination microscopy (SIM) is one of the most widely applied super-resolution microsco...
Of all 3D-super resolution techniques, structured illumination microscopy (SIM) provides the best co...
This thesis investigates ways for assessing the practical lateral resolution performance of imaging ...
Structured illumination microscopy (SIM) has become an important technique for optical super-resolut...
Three-dimensional fluorescence imaging is an essential tool in biology, used for everything from lon...
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A strai...
Heintzmann R, Huser T. Super-Resolution Structured Illumination Microscopy. CHEMICAL REVIEWS. 2017;1...
Structured illumination microscopy (SIM) is a very important super-resolution microscopy technique, ...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...
This version contains the updated results of the article " Deep-learning based denoising and reconst...
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A strai...