IP Library Granted Patent US 12,198,329
Granted Patent B2
US 12,198,329 · App. 17/103,414 · Granted Jan 14, 2025

Automated detection and characterization of micro-objects in microfluidic devices

Inventors: John A. Tenney (Emeryville, CA); Thomas M. Vetterli (Emeryville, CA); Hansohl E. Kim (Emeryville, CA)
G06T7/0012G06T7/174G06T7/30G06T7/11G06T2207/10056G06T2207/10064G06T2207/10152G06T2207/20081G06T2207/20084G06T2207/20224G06T2207/30024
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Quick Facts
Patent No.
US 12,198,329
App. No.
17/103,414
Granted
Jan 14, 2025
Kind
B2
Abstract

Methods are provided for the automated detection, characterization, and selection of micro-objects in a microfluidic device. In addition, methods are provided for grouping detected micro-objects into subgroups that share the same characteristics and, optionally, repositioning micro-objects in a selected sub-population within the microfluidic device. For example, micro-objects in a selected sub-population can be moved into sequestration pens. The methods also provide for visual displays of the micro-object characteristics, such as two- or three-dimensional graphs, and for user-based definition and/or selection of sub-populations of the detected micro-objects. In addition, non-transitory computer-readable medium in which a program is stored and systems for carrying out any of the disclosed methods are provided.

Claims (35)

1. A method for detecting and characterizing micro-objects in a microfluidic device, the method comprising:

receiving a first image and one or more second images of a region of interest in the microfluidic device, the first image comprising an illuminated image and the one or more second images comprising one or more non-illuminated images;

transforming each of the one or more second images to optically align the one or more second images with the first image;

processing pixel data in the first image using a machine learning algorithm to detect micro-objects present in the region of interest, wherein detecting each micro-object comprises identifying a boundary of the micro-object; and

detecting a signal located within each boundary of each detected micro-object in each one of the one or more second images, wherein each detected signal is associated with a reagent that specifically binds to a biological molecule comprised by one or more of the detected micro-objects.

2. The method of claim 1 , wherein at least one of the one or more second images is a fluorescent image, and wherein the detected signal in the one or more second images is a fluorescent signal.

3. The method of claim 2 , wherein each fluorescent image represents fluorescent signal from a non-overlapping portion of the visible light spectrum.

4. The method of claim 1 , wherein each of the one or more second images is a fluorescent image, and wherein the detected signal in each of the one or more second images is a fluorescent signal.

5. The method of claim 1 , wherein processing pixel data in the first image to detect micro-objects present in the region of interest comprises using the machine learning algorithm to generate a plurality of pixel masks from the first image for a corresponding plurality of micro-object characteristics, wherein each pixel mask comprises a set of pixel annotations, each pixel annotation of the set representing a probability that a corresponding pixel in the image represents the corresponding micro-object characteristic.

6. The method of claim 5 , wherein detecting the micro-objects comprises using a combination of pixel masks of the plurality of pixel masks.

7. The method of claim 5 , wherein the plurality of micro-object characteristics comprises at least: (i) micro-object center; (ii) micro-object edge; and (iii) non-micro-object.

8. The method of claim 7 , wherein detecting the micro-objects is based upon the pixel mask corresponding to the micro-object center characteristic or a combination of pixel masks that includes the pixel mask corresponding to the micro-object center characteristic.

9. The method of claim 1 , wherein there are at least two second images.

10. The method of claim 1 , further comprising:

grouping the detected micro-objects into sub-populations of micro-objects that share one or more of the same characteristics.

11. The method of claim 10 , wherein the detected micro-objects are grouped into sub-populations based upon their proximity in n-dimensional space, wherein each of the n dimensions is a measurable characteristic of the micro-objects.

12. The method of claim 1 , further comprising:

providing a visual display representing a distribution of at least one characteristic of the detected micro-objects.

13. The method of claim 12 , further comprising providing a user interface that allows the user to select a sub-population of the detected micro-objects and, optionally, to provide instruction(s) for repositioning the selected sub-population.

14. The method of claim 1 , further comprising increasing or decreasing the identified boundary of the micro-object.

15. The method of claim 1 , wherein the micro-objects are imaged within the microfluidic device, and wherein the pre-processing comprises subtracting out a repeating pattern produced by at least one component of the microfluidic device during imaging.

16. The method of claim 15 , wherein the pre-processing comprises applying a Fourier transform to the image to identify the repeating pattern.

17. The method of claim 15 , wherein the at least one component of the microfluidic device is a substrate surface.

18. The method of claim 15 , wherein the at least one component of the microfluidic device is a substrate surface including a photo-transistor array.

19. The method of claim 1 , wherein the micro-objects are living biological cells.

20. The method of claim 19 , wherein the living biological cells are: immunological cells; cells from a cell line or cancer cells; or oocytes, sperm, or embryos.

21. A system for automatically detecting micro-objects in a microfluidic device, comprising:

an image acquisition unit, comprising:

an imaging element configured to capture a first image and one or more second images of a region of interest in the microfluidic device, the first image comprising an illuminated image and the one or more second images comprising one or more non-illuminated images; and

an alignment engine configured to transform the second image to optically align the one or more second images with the first image, and

a micro-object detection and characterization unit communicatively connected to the image acquisition unit, comprising:

an image processing engine configured to process pixel data in the first image using a machine learning algorithm to detect micro-objects present in the region of interest, wherein detecting the micro-objects comprises identifying a boundary of each detected micro-object; and

a detection engine configured to detect a signal located within each boundary of each detected micro-object in each of the one or more second images, the first image comprising an illuminated image and the one or more second images comprising one or more non-illuminated images.

22. The system of claim 21 , further comprising:

a user interface, wherein the user interface is configured to allow the user to select a sub-population of the detected micro-objects and, optionally, to provide instruction(s) for repositioning the selected sub-population.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded Nov 30, 2023
From: PHENOMEX INC.; BIRD MERGERSUB CORPORATION
To: BRUKER CELLULAR ANALYSIS, INC.
Reel/Frame 065726/0624 →
CHANGE OF NAME Recorded Sep 20, 2023
From: BERKELEY LIGHTS, INC.
To: PHENOMEX INC.
Reel/Frame 064961/0794 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 24, 2020
From: TENNEY, JOHN A.; VETTERLI, THOMAS M.; KIM, HANSOHL E.
To: BERKELEY LIGHTS, INC.
Reel/Frame 054462/0070 →
Continuity (3)
Continuation PCTUS2019035046 · May 31, 2019
Provisional Application 62678791 · May 31, 2018
Related Publication 20210209752A1 · Jul 8, 2021
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