The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 17, 2023

Filed:

Sep. 08, 2022
Applicant:

Sartorius Bioanalytical Instruments, Inc., Bohemia, NY (US);

Inventors:

Daniel Appledorn, Bohemia, NY (US);

Eric Endsley, Bohemia, NY (US);

Nevine Holtz, Bohemia, NY (US);

Brad Neagle, Bohemia, NY (US);

David Rock, Bohemia, NY (US);

Kirk Schroeder, Bohemia, NY (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G06K 9/00 (2022.01); G06T 7/00 (2017.01); G06T 7/254 (2017.01); G16B 45/00 (2019.01); G06V 20/69 (2022.01);
U.S. Cl.
CPC ...
G06T 7/0012 (2013.01); G06T 7/254 (2017.01); G06V 20/698 (2022.01); G16B 45/00 (2019.02); G06T 2207/10056 (2013.01); G06T 2207/10064 (2013.01); G06T 2207/30024 (2013.01); G06T 2207/30072 (2013.01);
Abstract

Systems and methods are provided for automatically imaging and analyzing cell samples in an incubator. An actuated microscope operates to generate images of samples within wells of a sample container across days, weeks, or months. A plurality of images is generated for each scan of a particular well, and the images within such a scan are used to image and analysis metabolically active cells in the well. Tins analysis includes generating a 'range image' by subtracting the minimum intensity value, across the scan, for each pixel from the maximum intensity value. This range image thus emphasizes cells or portions of cells that exhibit changes in activity over a scan period (e.g., neurons, myocytes, cardiomyocytes) while de-emphasizing regions that exhibit consistently high intensities when images (e.g., regions exhibiting a great deal of autofluorescence unrelated to cell activity).


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