A system and method of screening biological specimens by at least one processor may include receiving a sample image depicting a biological specimen; applying a machine-learning (ML) based autoencoder on the sample image, wherein said autoencoder is trained to generate a reconstructed version of the sample image, via a latent feature vector; associating a latent feature of the latent feature vector to a corresponding visual phenotype of the biological specimen; and screening the biological specimen based on said association. Embodiments of the invention may subsequently modify a value of the latent feature to produce a vector set, comprising a plurality of latent feature vectors; apply a decoder portion of the autoencoder on the vector set, to produce a corresponding reconstructed image set, representing evolution or amplification of a visual phenotype of the biological specimen; and associate the latent feature to the visual phenotype based on the reconstructed image set.

A method for evaluating material properties includes an image processing for evaluation step, a material properties prediction step, and an evaluation step. The image processing for evaluation step includes scanning one or more images for evaluation of a material to be evaluated, creating a low-gradation image for evaluation by lowering gradation of the image for evaluation, and creating a virtual image by processing the low-gradation image for evaluation. The material properties prediction step includes extracting features for evaluation from the low-gradation image for evaluation, predicting a first material property of the material to be evaluated from the features for evaluation through a regression model, extracting a virtual-image feature from the virtual image, and predicting a second material property of the material to be evaluated from the virtual-image features through the regression model. The evaluation step is for comparing the first material property with the second material property.

Systems and methods are disclosed for receiving a digital image corresponding to a target specimen associated with a pathology category, wherein the digital image is an image of tissue specimen, determining a detection machine learning model, the detection machine learning model being generated by processing a plurality of training images to output a cancer qualification and further a cancer quantification if the cancer qualification is an confirmed cancer qualification, providing the digital image as an input to the detection machine learning model, receiving one of a pathological complete response (pCR) cancer qualification or a confirmed cancer quantification as an output from the detection machine learning model, and outputting the pCR cancer qualification or the confirmed cancer quantification.

A method of determining a clinical value for an individual based on a tumor in an image by an apparatus including processing circuitry may include executing, by the processing circuitry, instructions that cause the apparatus to determine a lymphocyte distribution of lymphocytes in the tumor based on the image; apply a classifier to the lymphocyte distribution to classify the tumor, the classifier having been trained to classify tumors into a class selected from at least two classes respectively associated with lymphocyte distributions; and determine the clinical value for the individual based on prognoses of individuals with tumors in the class into which the classifier classified the tumor.

A deep learning-based digital/virtual staining method and system enables the creation of digitally/virtually-stained microscopic images from label or stain-free samples. In one embodiment, the method of generates digitally/virtually-stained microscope images of label-free or unstained samples using fluorescence lifetime (FLIM) image(s) of the sample(s) using a fluorescence microscope. In another embodiment, a digital/virtual autofocusing method is provided that uses machine learning to generate a microscope image with improved focus using a trained, deep neural network. In another embodiment, a trained deep neural network generates digitally/virtually stained microscopic images of a label-free or unstained sample obtained with a microscope having multiple different stains. The multiple stains in the output image or sub-regions thereof are substantially equivalent to the corresponding microscopic images or image sub-regions of the same sample that has been histochemically stained.

A computer-implemented method may identify attributes of electronic images and display the attributes. The method may include receiving one or more electronic medical images associated with a pathology specimen, determining a plurality of salient regions within the one or more electronic medical images, determining a predetermined order of the plurality of salient regions, and automatically panning, using a display, across the one or more salient regions according to the predetermined order.

A non-invasive method of evaluating blood cell measurement and a non-invasive blood cell measurement evaluating system are provided. The non-invasive method of evaluating blood cell measurement includes providing of a dialysis tubing image datum of a subject, performing an image preprocessing step, performing a model predicting step and performing a determining and classifying step. The non-invasive blood cell measurement evaluating system includes an image capturing device and a processor electrically connected to the image capture device.

A computing device, method, system, and instructions in a non-transitory computer-readable medium for performing image analysis on 3D microscopy images to predict localization and/or labeling of various structures or objects of interest, by predicting the location in such images at which a dye or other marker associated with such structures would appear. The computing device, method, and system receives sets of 3D images that include unlabeled images, such as transmitted light images or electron microscope images, and labeled images, such as images captured with fluorescence tagging. The computing device trains a statistical model to associate structures in the labeled images with the same structures in the unlabeled light images. The processor further applies the statistical model to a new unlabeled image to generate a predictive labeled image that predicts the location of a structure of interest in the new image.

An image processing method according to the invention includes obtaining a ground truth image teaching a cell region occupied by a cell in an original image for each of a plurality of the original images obtained by bright-field imaging of the cell, generating a reverse image by reversing luminance of the original image at least for the cell region based on each original image, and constructing a classification model by performing machine learning using a set of the original image and the ground truth image corresponding to the original image and a set of the reverse image and the ground truth image corresponding to the original image as a basis of the reverse image respectively as training data.

Systems and methods for automated imaging and evaluation of image based features are disclosed herein. Method for automated imaging and evaluation of image based features can include receiving time-lapse images of at least one human embryo contained in a multi-well culture dish that can have a plurality of micro-wells. Image based features can be automatically generated from the time-lapse images of the human embryo. The image based features, which can include a cavitation feature, can be inputted into a classifier. The classifier can automatically and directly generate a viability prediction with the classifier from the image-based features.