Due to photo-toxicity, fluorescence microscopy imaging is a trade-off between signal to noise ratio, total observation time and spatio-temporal resolution. We propose a new and simple method to quantify the signal-dependent and the non-signal-dependent components of the noise from a single fluorescence microscopy image. No reference image is required and the computation time allows on line quantification of the noise. The estimation is realized in two steps. We first estimate the signal-dependent noise by fitting the intensity of an estimated noise free image, computed by median filtering, to the estimated global noise variance. The second step estimates the signal-independent noise as the background variance, by computing the variance of the most homogeneous sub blocks of the image. After having shown the validity of our approach, we then use this method to quantify the noise in one experiment and show its correlation with the qualitative expected image quality.
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http://dx.doi.org/10.1016/j.compmedimag.2010.04.001 | DOI Listing |
Nat Biotechnol
January 2025
Department of Automation, Tsinghua University, Beijing, China.
Super-resolution (SR) neural networks transform low-resolution optical microscopy images into SR images. Application of single-image SR (SISR) methods to long-term imaging has not exploited the temporal dependencies between neighboring frames and has been subject to inference uncertainty that is difficult to quantify. Here, by building a large-scale fluorescence microscopy dataset and evaluating the propagation and alignment components of neural network models, we devise a deformable phase-space alignment (DPA) time-lapse image SR (TISR) neural network.
View Article and Find Full Text PDFTissue microenvironments are extremely complex and heterogeneous. It is challenging to study metabolic interaction between the different cell types in a tissue with the techniques that are currently available. Here we describe a multimodal imaging pipeline that allows cell type identification and nanoscale tracing of stable isotope-labeled compounds.
View Article and Find Full Text PDFNano Lett
January 2025
Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016, India.
Structured illumination microscopy (SIM) is a robust wide-field optical nanoscopy technique. Several approaches are implemented to improve SIM's resolution capability (∼2-fold). However, achieving a high resolution with a large field of view (FOV) is still challenging.
View Article and Find Full Text PDFJ Biol Chem
January 2025
Department of Biomedical Science, Faculty of Health and Society, Malmö University, SE-205 06 Malmö, Sweden. Electronic address:
Apolipoprotein E (APOE) is distributed across various human tissues and plays a crucial role in lipid metabolism. Recent investigations have uncovered an additional facet of APOE's functionality, revealing its role in host defense against bacterial infections. To assess the antibacterial attributes of APOE3 and APOE4, we conducted antibacterial assays using P.
View Article and Find Full Text PDFJ Vis Exp
January 2025
Institute of Biochemistry and Molecular Biology, Hengyang Medical School, University of South China; National Health Commission Key Laboratory of Birth Defect Research and Preventio, Hunan Provincial Maternal and Child Health Care Hospital;
Both DNA replication and RNA transcription utilize genomic DNA as their template, necessitating spatial and temporal separation of these processes. Conflicts between the replication and transcription machinery, termed transcription-replication conflicts (TRCs), pose a considerable risk to genome stability, a critical factor in cancer development. While several factors regulating these collisions have been identified, pinpointing primary causes remains difficult due to limited tools for direct visualization and clear interpretation.
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