A laser scanning microscope includes: an objective that irradiates a specimen with a laser beam; a detection lens that condenses the laser beam that passes through the specimen, the detection lens being arranged so as to face the objective; an optical element that is removably arranged between an image plane on which the detection lens forms an image of the specimen and a first surface that is a lens surface closest to the specimen of the detection lens, the optical element converting the laser beam made incident on the optical element into diffused light or deflecting a portion of the laser beam made incident on the optical element; and a photodetector that detects detection light emitted from the optical element arranged between the image plane and the first surface to the image plane.

A SIngle-frame LAbel-free Cell Tomography (SILACT) system and methods are provided to reconstruct 3D Refractive Index (RI) distribution of cells at over 10,000 volumes/second while resolving subcellular compartments without fluorescence labelling. The SILACT includes a high-speed interference microscope with multiplex illumination and a fast reconstruction method utilizing a pre-trained physics-incorporating Deep Neural Network (DNN). With SILACT, it is demonstrated that 3D imaging cytometry at a throughput of over 20,000 cells/second can be achieved, and transient dynamics of Red Blood Cells (RBCs) undergoing shear-induced 3D deformation inside a microfluidic channel can be observed.

A system and method for optical sectioning in bright field microscopy (OSBM). The system includes a bright field optical microscope having automated change of focus, a substage condenser fitted with an adjustable aperture iris diaphragm, a digital camera that records the microscope image of samples, and one or more digital computers to perform digital image processing. The OSBM method comprises operating the microscope to Kohler illumination, using the iris diaphragm of the condenser to generate contrast in images, acquiring a Z-stack of images of the unstained sample, and applying a sequence of digital image processing filters to the Z-stack, resulting in optical sections from where the final three-dimensional (3D) image of the sample can be reconstructed by computational device. The final 3D images produced by this invention present quality comparable to that of available optical sectioning techniques that require sample labeling, such as light sheet fluorescence microscopy.

An ergonomic digital imaging system obviates the need for, and replaces, the standard microscope with binoculars for viewing images, thereby freeing the user from using his or her hands to manipulate images seen through the binoculars of the microscope, whereby the user can use his or her hands for other tasks, such as dental or other surgery, from a position away from the exhaled breath of the patient being treated. The images are maintained focused, no matter how close or far the viewer is to the viewing display screen. The system is collapsible and portable, so that specialists can take the system from office to office, a plug and play work environment. The extended maneuverability of the camera head results in simple and fast patient positioning, and the camera and display module adjust for any comfortable sit or stand ergonomics of the practitioner.

An analyzer of a component in a sample fluid includes an optical source and an optical detector defining a beam path of a beam, wherein the optical source emits the beam and the optical detector measures the beam after partial absorption by the sample fluid, a fluid flow cell disposed on the beam path defining an interrogation region in the a fluid flow cell in which the optical beam interacts with the sample fluid and a reference fluid; and wherein the sample fluid and the reference fluid are in laminar flow, and a scanning system that scans the beam relative to the laminar flow within the fluid flow cell, wherein the scanning system scans the beam relative to both the sample fluid and the reference fluid.

A large-field-of-view, high-throughput and high-resolution pathological section analyzer includes an image collector for collecting a set of computing microscopic images of a pathological section sample; a data preprocessing circuit for iteratively updating the set of computing microscopic images by a multi-height phase recovery algorithm to obtain a low-resolution reconstructed image; an image super-resolution circuit for super-resolving the low-resolution reconstructed image according to a pre-trained super-resolution model to obtain a high-resolution reconstructed image; and an image analysis circuit for automatically analyzing the high-resolution reconstructed image according to different tasks, and specifically selecting different analysis models according to the different tasks to obtain corresponding auxiliary diagnosis results. Imaging visual field of the pathological section analyzer is hundreds of times that of the traditional optical microscope, a deep learning network is adopted to analyze pathological conditions of unstained pathological sections, so that the analysis process of pathological sections is simplified.

Examples relate to a microscope system (100; 400) and to a corresponding system (110), method and computer program for a microscope system. The system comprises one or more processors (114) and one or more storage devices (116). The system is configured to determine a quality indicator of a quality of image data of a fluorescence imaging sensor (122) of a microscope (120) of the microscope system. The system is configured to identify, for one or more user settings of the microscope, a range of values that are suitable in view of the quality indicator. The system is configured to control a change of the one or more user settings based on the range of values that are suitable in view of the quality indicator.

The invention relates to a detection device (2) for a laser scanning microscope, the detection device (2) having a light inlet (4), at least one filter module (14) and at least one spatially resolving detector (22) and being configured to guide light from the light inlet (4) to the filter module (14) and from there to the spatially resolving detector (22), at least one filter module (14) being designed as a continuous filter module with two continuously tunable filter elements (16), and at least one compensator element (26) being arranged optically downstream of the continuous filter module (14), by means of which a focal position of light on the spatially resolving detector (22) can be adjusted.

Systems, methods and devices are implemented for microscope imaging solutions. One embodiment of the present disclosure is directed toward an epifluorescence microscope. The microscope includes an image capture circuit including an array of optical sensor. An optical arrangement is configured to direct excitation light of less than about 1 mW to a target object in a field of view of that is at least 0.5 mm.sup.2 and to direct epi-fluorescence emission caused by the excitation light to the array of optical sensors. The optical arrangement and array of optical sensors are each sufficiently close to the target object to provide at least 2.5 μm resolution for an image of the field of view.

A scanner for scanning a QA test slide as part of a stain QA method, and method of using the scanner are described. The scanner comprises a housing defining an interior of the scanner, a slide holder within the housing and configured to receive a QA test slide, a digital camera within the housing and arranged to capture an image of the QA test slide when located in the slide holder, and a light source within the housing and arranged to illuminate both a rear side and a front side of the QA test slide when located in the slide holder.