A biological information detection device includes: a video capture unit, a blood flow analysis unit, a local pulse wave detection unit, a pulse wave propagation velocity calculation unit, and a blood pressure estimation unit. The video capture unit obtains video information on a face of a living body. The blood flow analysis unit analyzes video data of at least three skin areas in the video information, as blood flow information. The local pulse wave detection unit is provided for each skin area to calculate pulse information based on the blood flow information sequenced chronologically. The pulse wave propagation velocity calculation unit calculates a pulse wave propagation velocity based on a phase difference between pieces of the pulse information at each skin area calculated by the local pulse wave detection unit. The blood pressure estimation unit estimates blood pressure based on the pulse wave propagation velocity.

An imaging system and method for microbial growth detection, counting or identification. One colony may be contrasted in an image that is not optimal for another type of colony. The system and method provides contrast from all available material through space (spatial differences), time (differences appearing over time for a given capture condition) and color space transformation using image input information over time to assess whether microbial growth has occurred for a given sample.

Fluorescence based tracking of a light-emitting marker in a bodily fluid stream is conducted by: providing a light-emitting marker into a fluid stream; establishing field of view monitoring by placement of a sensor, such as a high speed camera, at a region of interest; recording image data of light emitted by the marker at the region of interest; determining time characteristics of the light output of the marker traversing the field of view; and calculating flow characteristics based on the time characteristics. Furthermore generating a velocity vector map may be conducted using a cross correlation technique, leading and falling edge considerations, subtraction, and/or thresholding.

One variation of method for monitoring growth of plants within a facility includes: aggregating global ambient data recorded by a suite of fixed sensors, arranged proximal a grow area within the facility, at a first frequency during a grow period; extracting interim outcomes of a set of plants, occupying a module in the grow area, from module-level images recorded by a mover at a second frequency less than the first frequency while interfacing with the module during the period of time; dispatching the mover to autonomously deliver the module to a transfer station; extracting interim outcomes of the set of plants from plant-level images recorded by the transfer station while sequentially transferring plants out of the module at the conclusion of the grow period; and deriving relationships between ambient conditions, interim outcomes, and final outcomes from a corpus of plant records associated with plants grown in the facility.

Some aspects include a method of detecting change in biological subject matter of a patient positioned within a low-field magnetic resonance imaging device, the method comprising: while the patient remains positioned within the low-field magnetic resonance device: acquiring first magnetic resonance image data of a portion of the patient; acquiring second magnetic resonance image data of the portion of the patient subsequent to acquiring the first magnetic resonance image data; aligning the first magnetic resonance image data and the second magnetic resonance image data; and comparing the aligned first magnetic resonance image data and second magnetic resonance image data to detect at least one change in the biological subject matter of the portion of the patient.

In some embodiments, a set of eye images related to a subject may be provided to a prediction model. A first prediction may be obtained via the prediction model, where the first prediction is derived from a first eye image and indicates whether an eye condition is present in the subject. A second prediction may be obtained via the prediction model, where the second prediction is derived from a second eye image and indicates that the eye condition is present in the subject. An aspect associated with the first prediction may be adjusted via the prediction model based on the second prediction's indication that the eye condition is present in the subject. One or more predictions related to at least one eye condition for the subject may be obtained from the prediction model, where the prediction model generates the predictions based on the adjustment of the first prediction.

There is provided a medical imaging processing device, comprising: at least one hardware processor executing a code for: iteratively generating instructions for iterative adjustment of presentation parameter(s) of a 2D frame of the 3D anatomical image presented on the display, for creating a sequence of adapted 2D frames of the 3D anatomical image, the instructions transmitted from the medical imaging processing device to a physical input interface of at least one of the client terminal and display, for each respective 2D frame: capturing the respective 2D frame from video signals transmitted from the client terminal to the display, analyzing the respective captured 2D frame for extraction of a 2D anatomical image, analyzing the respective captured 2D frame to identify metadata element(s), converting the metadata element(s) into converted metadata value(s), and formatting the extracted 2D anatomical images and associated converted metadata values for reconstruction of the 3D anatomical image.

A method of quantifying changes in a visceral organ comprises acquiring first (310) and second (410) medical scans of a visceral organ at first and second timepoints. At least part of the visceral organ in the first medical scan is parcellated into a first set of one or more subregions (420), based on image content, each subregion comprising a plurality of voxels. The first medical scan (310) is aligned to the second medical scan (410), before or after parcellating the first medical scan (310). Then the second medical scan is parcellated into a second set of one or more subregions. A metric is evaluated for a subregion in the first medical scan (310), and for the corresponding subregion in the second medical scan (410). A difference in the metric values provides a measure of a change that has occurred in the subregion, between the first and second timepoints.

A radiographic imaging apparatus (100) is configured to generate movement maps (30) of pixels (21) belonging to a first image (11) based on the first image (11) and a second image (12) captured at different times, to move a pixel (21) of the first image (11) based on a smoothed movement map (30a) in which high-frequency components of the movement maps (30) have been suppressed in a spatial direction and generate a deformed image (11a), and to combine the deformed image (11a) and the second image (12).

In the present invention, a first image acquisition means 81 acquires a first image of an inspection target including an abnormal part. A second image acquisition means 82 acquires a second image of the inspection target captured earlier than the time when the first image is captured. A learning data generation means 83 generates learning data indicating that the second image includes an abnormal part. A learning means 84 learns a discrimination dictionary by using the learning data generated by the learning data generation means 83.