Neuronal Pattern Analysis in Golgi-Stained Images

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Solution Overview

Problem

Golgi staining techniques, such as brightfield imaging microscopy, face challenges in downstream image analysis due to blurry out-of-focus objects and physical shadows from neuronal structures, which reduce the signal-to-noise ratio and complicate differentiation between neuronal structures.

Innovation Solution

A computer-implemented method for identifying neuronal patterns in Golgi-stained images involves obtaining a dataset of Golgi-stained neuronal structures, determining auxiliary datasets based on specific types of neuronal structures, and analyzing these datasets using machine learning algorithms such as convolutional neural networks (CNNs) and pixel classification methods to enhance visibility and accuracy of neuronal structures.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Illumination intensity

If Golgi staining is used with brightfield imaging microscopy, then neuronal structures can be visualized, but the dark and opaque nature of the stain causes physical shadows that reduce the signal-to-noise ratio

Engineering Contradiction:
Improvesignal-to-noise ratioVSAvoidphysical shadows from neuronal structures
Core Design Contradiction:
Illumination intensityVSObject-generated harmful factors

Solution Approach 1:

The patent replaces traditional brightfield optical microscopy with computational imaging methods. Instead of relying on optical contrast mechanisms that produce shadows, the system uses multiple imaging modalities (phase contrast, differential interference contrast, fluorescence) combined with computational algorithms to reconstruct neuronal structures without physical shadowing artifacts.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent changes the imaging parameters by using multiple different contrast mechanisms (phase, differential interference, fluorescence) rather than relying on a single brightfield modality. This multi-parameter approach allows the system to overcome the limitations of dark and opaque staining by capturing information from different physical domains.

Inventive Principle:
Principle #35Parameter changes

2Productivity

If traditional image analysis is applied to Golgi-stained images, then processing can be performed, but objects out of focus appear as blurry objects on multiple planes complicating analysis

Engineering Contradiction:
Improveimage analysis processingVSAvoiddifferentiation between neuronal structures
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent segments the imaging process into multiple specialized channels (phase contrast for structural overview, differential interference contrast for edge detection, fluorescence for specific labeling) rather than attempting to capture all information in a single image. This segmentation allows each modality to optimize for its specific function, improving overall measurement precision.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent adds the temporal dimension by capturing images at multiple focal planes and using computational algorithms to reconstruct three-dimensional neuronal structures. This transforms the problem from analyzing blurry 2D projections to reconstructing clear 3D models, thereby improving differentiation precision.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Data Source

PatentUS20250157232A1Method for analyzing neuronal patterns in golgi-stained images
Publication Date: 2025.05.15 LEICA MICROSYSTEMS CMS GMBH
  • US20250157232A1 patent drawing
  • US20250157232A1 patent drawing
  • US20250157232A1 patent drawing

AI summary

A first aspect of this disclosure is related to a computer-implemented method for identifying neuronal patterns in an image,comprising the steps:obtaining a first data set with Golgi-stained neuronal structures;based on the first data set, determining a first auxiliary data set, AR1, based on a first type of neuronal structure and a second auxiliary data set, AR2, based on a second type of neuronal structure;analyzing AR1 with a first method to identify information related to the first type of neuronal structure in AR1;analyzing AR2 with a second method to identify information related to the second type of neuronal structure in AR2;generating a second data set with the identified information related to the first and second type of neuronal structures.