scholarly journals Understanding Complex Single Molecule Emission Patterns with Deep Learning

2019 ◽  
Vol 116 (3) ◽  
pp. 281a
Author(s):  
Peiyi Zhang ◽  
Sheng Liu ◽  
Abhishek Chaurasia ◽  
Donghan Ma ◽  
Michael J. Mlodzianoski ◽  
...  
2021 ◽  
Author(s):  
Artur Speiser ◽  
Lucas-Raphael Müller ◽  
Philipp Hoess ◽  
Ulf Matti ◽  
Christopher J. Obara ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Jieming Li ◽  
Leyou Zhang ◽  
Alexander Johnson-Buck ◽  
Nils G. Walter

AbstractTraces from single-molecule fluorescence microscopy (SMFM) experiments exhibit photophysical artifacts that typically necessitate human expert screening, which is time-consuming and introduces potential for user-dependent expectation bias. Here, we use deep learning to develop a rapid, automatic SMFM trace selector, termed AutoSiM, that improves the sensitivity and specificity of an assay for a DNA point mutation based on single-molecule recognition through equilibrium Poisson sampling (SiMREPS). The improved performance of AutoSiM is based on accepting both more true positives and fewer false positives than the conventional approach of hidden Markov modeling (HMM) followed by hard thresholding. As a second application, the selector is used for automated screening of single-molecule Förster resonance energy transfer (smFRET) data to identify high-quality traces for further analysis, and achieves ~90% concordance with manual selection while requiring less processing time. Finally, we show that AutoSiM can be adapted readily to novel datasets, requiring only modest Transfer Learning.


2021 ◽  
Author(s):  
Artur Speiser ◽  
Lucas-Raphael Müller ◽  
Philipp Hoess ◽  
Ulf Matti ◽  
Christopher J. Obara ◽  
...  

2021 ◽  
Author(s):  
Amin Zehtabian ◽  
Paul Markus Müller ◽  
Maximilian Goisser ◽  
Leon Obendorf ◽  
Lea Jänisch ◽  
...  

The combination of image analysis and fluorescence superresolution microscopy methods allows for unprecedented insight into the organization of macromolecular assemblies in cells. Advances in deep learning-based object recognition enables the automated processing of large amounts of data, resulting in high accuracy through averaging. However, while the analysis of highly symmetric structures of constant size allows for a resolution approaching the dimensions of structural biology, deep learning methods are prone to different forms of bias. A biased recognition of structures may prohibit the development of readouts for processes that involve significant changes in size or shape of amorphous macromolecular complexes. What is required to overcome this problem is a detailed investigation of potential sources of bias and the rigorous testing of trained models using real or simulated data covering a wide dynamic range of possible results. Here we combine single molecule localization-based superresolution microscopy of septin ring structures with the training of several different deep learning models for a quantitative investigation of bias resulting from different training approaches and finally quantitative changes in septin ring structures. We find that trade-off exists between measurement accuracy and the dynamic range of recognized phenotypes. Using our trained models, we furthermore find that septin ring size can be explained by the number of subunits they are assembled from alone. Our work provides a new experimental system for the investigation of septin polymerization.


Author(s):  
Johannes Thomsen ◽  
Magnus B. Sletfjerding ◽  
Stefano Stella ◽  
Bijoya Paul ◽  
Simon Bo Jensen ◽  
...  

AbstractSingle molecule Förster Resonance energy transfer (smFRET) is a mature and adaptable method for studying the structure of biomolecules and integrating their dynamics into structural biology. The development of high throughput methodologies and the growth of commercial instrumentation have outpaced the development of rapid, standardized, and fully automated methodologies to objectively analyze the wealth of produced data. Here we present DeepFRET, an automated standalone solution based on deep learning, where the only crucial human intervention in transiting from raw microscope images to histogram of biomolecule behavior, is a user-adjustable quality threshold. Integrating all standard features of smFRET analysis, DeepFRET will consequently output common kinetic information metrics for biomolecules. We validated the utility of DeepFRET by performing quantitative analysis on simulated, ground truth, data and real smFRET data. The accuracy of classification by DeepFRET outperformed human operators and current commonly used hard threshold and reached >95% precision accuracy only requiring a fraction of the time (<1% as compared to human operators) on ground truth data. Its flawless and rapid operation on real data demonstrates its wide applicability. This level of classification was achieved without any preprocessing or parameter setting by human operators, demonstrating DeepFRET’s capacity to objectively quantify biomolecular dynamics. The provided a standalone executable based on open source code capitalises on the widespread adaptation of machine learning and may contribute to the effort of benchmarking smFRET for structural biology insights.


2020 ◽  
Author(s):  
Gili Dardikman-Yoffe ◽  
Yonina C. Eldar

AbstractThe use of photo-activated fluorescent molecules to create long sequences of low emitter-density diffraction-limited images enables high-precision emitter localization. However, this is achieved at the cost of lengthy imaging times, limiting temporal resolution. In recent years, a variety of approaches have been suggested to reduce imaging times, ranging from classical optimization and statistical algorithms to deep learning methods. Classical methods often rely on prior knowledge of the optical system and require heuristic adjustment of parameters or do not lead to good enough performance. Deep learning methods proposed to date tend to suffer from poor generalization ability outside the specific distribution they were trained on, and require learning of many parameters. They also tend to lead to black-box solutions that are hard to interpret. In this paper, we suggest combining a recent high-performing classical method, SPARCOM, with model-based deep learning, using the algorithm unfolding approach which relies on an iterative algorithm to design a compact neural network considering domain knowledge. We show that the resulting network, Learned SPARCOM (LSPARCOM), requires far fewer layers and parameters, and can be trained on a single field of view. Nonetheless it yields comparable or superior results to those obtained by SPARCOM with no heuristic parameter determination or explicit knowledge of the point spread function, and is able to generalize better than standard deep learning techniques. It even allows producing a high-quality reconstruction from as few as 25 frames. This is due to a significantly smaller network, which also contributes to fast performance - 5× improvement in execution time relative to SPARCOM, and a full order of magnitudes improvement relative to a leading competing deep learning method (Deep-STORM) when implemented serially. Our results show that we can obtain super-resolution imaging from a small number of high emitter density frames without knowledge of the optical system and across different test sets. Thus, we believe LSPARCOM will find broad use in single molecule localization microscopy of biological structures, and pave the way to interpretable, efficient live-cell imaging in a broad range of settings.


Optica ◽  
2018 ◽  
Vol 5 (4) ◽  
pp. 458 ◽  
Author(s):  
Elias Nehme ◽  
Lucien E. Weiss ◽  
Tomer Michaeli ◽  
Yoav Shechtman

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