The present disclosure describes a computer implemented method, a system, and a computer program product of measuring light scattering of a sample.

Provided herein are an optical test platform and corresponding method of manufacturing the same. The test platform may include a shell defining a cavity for receiving a sample tube, a first aperture, and a second aperture. The first aperture and the second aperture of the shell may each be configured to optically couple the cavity with an exterior of the shell. The test platform may further include a first window and a second window embedded in the shell. The first window may seal a first aperture and the second window may seal a second aperture. The first window and second window may each permit the optical coupling of the cavity with the exterior of the shell. The first window and the second window may be optically coupled via the cavity, and the shell may prohibit optical coupling between the first window and the second window through the shell.

The present disclosure describes a computer implemented method, a system, and a computer program product of measuring light scattering of a sample.

The invention relates to a method for inspecting a coated surface for a surface defect. The method comprises: using (102) a device (200, 300, 400, 700, 800, 900) for covering the coated surface to be inspected, the device being configured to create an enclosed space to isolate the surface coating to be inspected from ambient illumination in order to provide predefined photographic acquisition conditions within the enclosed space; acquiring (104) a photo of the coated surface being within the enclosed space; and inspecting (106) the photo for the presence of the surface defect.

A method of analyzing a tissue specimen is provided. The method includes imaging a tissue specimen to produce autofluorescence images acquired at different excitation and emission wavelengths, and/or reflectance images, using data produced during the imaging to identify one or more regions of interest within the tissue specimen, and performing an omics profiling on the identified one or more regions of interest within the tissue specimen to produce information relating to the tissue specimen.

An imaging reflectometer includes a source module configured to generate a plurality of input beams at different nominal wavelengths. An illumination pupil having a first numerical aperture (NA) is arranged so that each of the plurality of input beams passes through the illumination pupil. A large field lens is configured to receive at least a portion of each of the plurality of input beams and provide substantially telecentric illumination over a sample being imaged. The large field lens is also configured to receive reflected portions of the substantially telecentric illumination reflected from the sample. The reflected portions pass through an imaging pupil having a second NA that is lower than the first NA and are received by an imaging sensor module that generates image information.

A tomography method, system, and apparatus based on time-domain spectroscopy are provided. A light emitter is controlled to emit a pulse beam to scan a cross-section of an object to be measured while using a light receiver to detect the pulse beam passing through the object to be measured, so as to obtain time-domain pulse signals at locations of a scan path. A scan angle is repeatedly changed to perform the scanning and detecting steps, so as to collect the time-domain pulse signals of multiple angles of the cross-section as a time information set. Features are retrieved from the time-domain pulse signals using kernels of a trained machine learning model, which is trained with time information sets and corresponding ground truth images of cross-sections to learn the kernels for retrieving the features. The retrieved features are converted into a spatial domain to reconstruct a cross-sectional image of the object.

A spatial gradient-based fluorometer featuring a signal processor or processing module configured to: receive signaling containing information about light reflected off fluorophores in a liquid and sensed by a linear sensor array having a length and rows and columns of optical elements; and determine corresponding signaling containing information about a fluorophore concentration of the liquid a fluorophore concentration of the liquid that depends on a spatial gradient of the light reflected and sensed along the length of the linear sensor array, based upon the signaling received

Instruments, systems, and methods for measuring optical density of microbiological samples are provided. In particular, optical density instruments providing improved safety, efficiency, comfort, and convenience are provided. Such optical density instruments include a handheld portion and a base station. The optical density instruments may be used in systems and methods for measuring optical density of biological samples.

A LIBS analysis system comprises a focusing lens arrangement having a focal plane; a laser for propagating a laser beam through the focusing lens arrangement to be focused at the focal plane; a detector for generating an output that is proportional to an intensity of incident electromagnetic radiation that is incident on the detector; a translation mechanism configured to cause a relative movement of the sample holder and the focusing lens arrangement to vary a position of the focal plane along the optical path with respect to the sample holder; and a controller configured to automatically control the translation mechanism to cause the relative movement of the sample holder and the focusing lens arrangement to achieve an optimum position at which the focal plane and an analysis region of the upper surface intersecting the optical path are at or are close to coincidence.