G01N2201/12761

SWEPT FREQUENCY FLUOROMETER
20210364433 · 2021-11-25 ·

A swept frequency fluorometer having a signal processor or processing module configured to:

receive signaling containing information about reflected light off one or more fluorescence species-of-interest in a liquid sample that is swept with light having a variable frequency range, the information including a characteristic optical frequency corresponding to a fluorescence species-of-interest in the liquid, and a characteristic/lifetime optical frequency corresponding to a distinct fluorescence lifetime in which the fluorescence species-of-interest remains in an excited state; and

provide corresponding signaling containing information about an identity of the fluorescence species-of-interest detected and distinguished from overlapping fluorescence species in the liquid using the characteristic/lifetime optical frequency, based upon the signaling received

DEVICES, SYSTEMS, AND METHODS FOR FLUORESCENCE LIFETIME IMAGING MICROSCOPY

The invention provides novel non-invasive in vitro methods for assessing the metabolic condition of oocytes and/or embryos with fluorescence lifetime imaging microscope, that can be used, for example, in assessment of oocytes and embryos in assisted reproductive technologies.

FLUORESCENCE OBSERVATION APPARATUS AND FLUORESCENCE OBSERVATION METHOD

A fluorescence observation apparatus according to an embodiment of the present technology includes a stage, an excitation section, and a spectroscopic imaging section. The stage is capable of supporting a fluorescently stained pathological specimen. The excitation section irradiates the pathological specimen on the stage with a plurality of line illuminations of different wavelengths, the plurality of line illuminations being a plurality of line illuminations situated on different axes and parallel to a certain-axis direction. The spectroscopic imaging section includes at least one imaging device capable of separately receiving pieces of fluorescence respectively excited with the plurality of line illuminations.

SAMPLE ANALYSIS APPARATUS AND SAMPLE ANALYSIS PROGRAM
20210201140 · 2021-07-01 ·

A learning model creation unit 12A that creates a learning model using parameters of a plurality of fitting functions corresponding to a generation source of a composite waveform fit to a frequency spectrum obtained by spectroscopic measurement of a terahertz wave, and a sample information prediction unit 22A that applies a parameter obtained for a sample to be predicted to the learning mode thereby predicting information about the sample to be predicted are included, and the information about the sample to be predicted can be more accurately predicted using a learning model in which a feature quantity representing a property of a sample is reflected as the parameters of the plurality of fitting functions corresponding to the generation source of the composite waveform fit to the frequency spectrum.

SYSTEM AND METHOD FOR ACQUISITION AND PROCESSING OF MULTIPLEXED FLUORESCENCE IN-SITU HYBRIDIZATION IMAGES
20210199584 · 2021-07-01 ·

In acquisition of spatial transcriptomic information, a plurality of images representing a common field of view of a sample are obtained and registered. Each pixel of the registered images is decoded by identifying a code word from a plurality of code words in a code book that provides a best match to data values in the plurality of registered images for the pixel. For each code word identified as a best match and each pixel, whether a bit ratio for an image word for the pixel meets a threshold for the code word is determined. The image word is formed from the data values in the plurality of registered images for the pixel. For at least one pixel that is determined to meet the threshold, a gene associated with the code word is determined. Pixels for which the bit ratio does not meet the threshold are screened.

SYSTEM FOR ACQUISITION AND PROCESSING OF MULTIPLEXED FLUORESCENCE IN-SITU HYBRIDIZATION IMAGES
20210181111 · 2021-06-17 ·

In a fluorescent in-situ hybridization imaging system performs, as nested loops, the following: (1) a valve sequentially couples a flow cell to a plurality of different reagent sources to expose the sample to a plurality of different reagents, (2) for each reagent of the plurality of different reagents, a motor sequentially positions the fluorescence microscope relative to sample at a plurality of different fields of view, (3) for each field of view of the plurality of different fields of view, a variable frequency excitation light source sequentially emits a plurality of different wavelengths, (4) for each wavelength of the plurality of different wavelengths, an actuator sequentially positions the fluorescence microscope relative to sample at a plurality of different vertical heights, and (5) for each vertical height of the plurality of different vertical heights, an image is obtained.

REGISTRATION TECHNIQUES FOR MULTIPLEXED FLUORESCENCE IN-SITU HYBRIDIZATION IMAGES
20210182531 · 2021-06-17 ·

For acquisition of spatial transcriptomic information, one or more filters are applied to deconvolution is performed on each image of a plurality of images to generate a plurality of filtered images, and registration of the plurality of filtered images is performed to generate a plurality of registered and filtered images. For each pixel of at least two pixels of the plurality of registered and filtered images, the pixel is decoded by identifying a code word from a plurality of code words in a code book that provides a best match to data values in the plurality of registered and filtered images for the pixel. For each pixel of at least two pixels, a gene is associated with the code word is determined and an indication that the gene is expressed at the pixel is stored.

IMAGE PROCESSING TECHNIQUES IN MULTIPLEXED FLUORESCENCE IN-SITU HYBRIDIZATION
20210183034 · 2021-06-17 ·

A fluorescent in-situ hybridization imaging and analysis system includes a flow cell to contain a sample to be exposed to fluorescent probes in a reagent, a fluorescence microscope to obtain sequentially collect a plurality of images of the sample at a plurality of different combinations of imaging parameters, and a data processing system. The data processing system includes an online pre-processing system configured to sequentially receive the images from the fluorescence microscope as the images are collected and perform on-the-fly image pre-processing to remove experimental artifacts of the image and to provide RNA image spot sharpening, and an offline processing system configured to, after the plurality of images are collected, perform registration of images having a same field of view and to decode intensity values in the plurality of images to identify expressed genes.

GAS SENSORS

A gas sensor for measuring concentration of a predetermined gas includes a light source (2) arranged to emit pulses of light, a measurement volume (10), a detector (4) arranged to receive light that has passed through the measurement volume (10), and an adaptable filter (6) disposed between the light source (2) and the detector (4). The gas sensor has a measurement state in which it passes at least one wavelength band which is absorbed by the gas and a reference state in which said wavelength band is attenuated relative to the measurement state. A controller is connected to each of the light source, the detector and the adaptable filter to change the adaptable filter between one of said measurement state and said reference state to the other at least once during a gas sensor operation period.

MULTI-ANALYTE CONCENTRATION ESTIMATION FOR FIXED-WAVELENGTH SPECTROSCOPY
20210151131 · 2021-05-20 ·

The absorbance of a mixed sample at multiple wavelengths is determined and the concentrations of the sample constituents deduced from the observed absorbances. Assuming the sample constituents are known, these wavelengths correspond to peak absorption wavelengths for the constituents. Rather than attempt to generate an analytical relationship among absorbance levels and constituent concentrations, a database of absorbance values for each wavelength, spanning the range of possible analyte concentrations, is employed instead. In general, the wavelengths utilized correspond to peak absorption wavelengths for each of the analytes.