IP Library Granted Patent US 11,501,432
Granted Patent B2
US 11,501,432 · App. 16/913,765 · Granted Nov 15, 2022

Spiking retina microscope

Inventors: William Mark Severa (Albuquerque, NM); John Darby Smith (Albuquerque, NM); Suma George Cardwell (Albuquerque, NM)
Assignee: National Technology & Engineering Solutions of Sandia, LLC
G06T7/0012G06K9/6267G06T5/002G06T7/20H04N5/2253H04N5/2254H04N7/18G06T2207/10056G06T2207/30024
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Quick Facts
Patent No.
US 11,501,432
App. No.
16/913,765
Granted
Nov 15, 2022
Kind
B2
Abstract

A spiking retina microscope comprising microscope optics and a neuromorphic imaging sensor. The microscope optics are configured to direct a magnified image of a specimen onto the neuromorphic imaging sensor. The neuromorphic imaging sensor comprises a plurality of sensor elements that are configured to generate spike signals in response to integrated light from the magnified image reaching a threshold. The spike signals may be processed by a processor unit to generate a result, such as tracking biological particles in a specimen comprising biological material.

Claims (26)

1. A spiking retina microscope, comprising:

microscope optics; and

a neuromorphic imaging sensor, wherein the microscope optics are configured to direct a magnified image of a specimen onto the neuromorphic imaging sensor and the neuromorphic imaging sensor comprises a plurality of sensor elements that are configured to generate spike signals in response to integrated light from the magnified image reaching a threshold, wherein each of the spike signals identifies a location in the magnified image and a time of occurrence of the spike signal.

2. The spiking retina microscope of claim 1 , further comprising illumination of the specimen.

3. The spiking retina microscope of claim 1 , wherein the plurality of sensor elements are leaky sensor elements.

4. The spiking retina microscope of claim 1 , wherein the plurality of sensor elements are non-leaky sensor elements.

5. The spiking retina microscope of claim 1 , further comprising a processor unit configured to process the spike signals to generate a result.

6. The spiking retina microscope of claim 5 , wherein the processor unit is an embedded coprocessor on the neuromorphic imaging sensor.

7. The spiking retina microscope of claim 5 , wherein the processor unit is a computer or a neuromorphic processor.

8. The spiking retina microscope of claim 5 , wherein the processor unit is configured to process the spike signals to track biological particles in the specimen comprising biological material.

9. A method of examining a specimen, comprising:

placing the specimen in a spiking retina microscope, wherein the spiking retina microscope comprises microscope optics and a neuromorphic imaging sensor, such that a magnified image of the specimen is directed from the microscope optics onto the neuromorphic imaging sensor; and

processing spike signals from the neuromorphic imaging sensor to generate a result, wherein the spike signals are generated by a plurality of sensor elements in the neuromorphic imaging sensor in response to integrated light from the magnified image reaching a threshold, and wherein each of the spike signals identifies a location in the magnified image and a time of occurrence of the spike signal.

10. The method of claim 9 , further comprising illuminating the specimen.

11. The method of claim 9 , wherein the plurality of sensor elements are leaky sensor elements.

12. The method of claim 9 , wherein the plurality of sensor elements are non-leaky sensor elements.

13. The method of claim 9 , wherein processing the spike signals comprises processing the spike signals by an embedded coprocessor on the neuromorphic imaging sensor.

14. The method of claim 9 , wherein processing the spike signals comprises processing the spike signals by a processor unit comprising a computer or a neuromorphic processor.

15. The method of claim 9 , wherein processing the spike signals comprises processing the spike signals using a data cube or back projection.

16. The method of claim 9 , wherein processing the spike signals to generate the result comprises tracking an object in the specimen, noise reduction, background subtraction, or classification of an object in the specimen.

17. A method of tracking biological particles, comprising:

placing a specimen comprising biological material in a spiking retina microscope, wherein the spiking retina microscope comprises microscope optics and a neuromorphic imaging sensor, such that a magnified image of the specimen is directed from the microscope optics onto the neuromorphic imaging sensor; and

processing spike signals from the neuromorphic imaging sensor to track the biological particles in the biological material, wherein the spike signals are generated by a plurality of sensor elements in the neuromorphic imaging sensor in response to integrated light from the magnified image reaching a threshold, and wherein each of the spike signals identifies a location in the magnified image and a time of occurrence of the spike signal.

18. The method of claim 17 , wherein the biological particles comprise biological cells or biological particles within biological cells.

19. The spiking retina microscope of claim 1 , wherein the neuromorphic imaging sensor comprises a dynamic vision sensor (DVS) or a dynamic and active-pixel vision sensor (DAVIS).

20. The spiking retina microscope of claim 1 , wherein the neuromorphic imaging sensor comprises a spiking processing array (SPARR).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2020
From: SEVERA, WILLIAM MARK; SMITH, JOHN DARBY; CARDWELL, SUMA GEORGE
To: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
Reel/Frame 054393/0178 →
CONFIRMATORY LICENSE Recorded Jul 17, 2020
From: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 053235/0965 →
Continuity (1)
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