Cytometric Data Scaling for Signal-to-Noise Optimization

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Solution Overview

Problem

Flow-type particle detection and analysis systems face challenges in effectively distinguishing between signal and noise, particularly with high dimensionality cytometric data, which affects the accuracy of particle characterization and population identification.

Innovation Solution

The method involves obtaining cytometric data, identifying a parameter of interest, specifying positive and negative measurement intervals, and scaling the data by transforming the parameter based on these intervals, using techniques such as adaptive scaling to improve signal-to-noise ratios.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If high dimensionality cytometric data is analyzed without scaling, then more parameters can be measured and analyzed, but signal-to-noise ratio deteriorates and noise affects particle clustering

Engineering Contradiction:
Improvedimensionality of cytometric dataVSAvoidsignal-to-noise ratio
Core Design Contradiction:
Adaptability or versatilityVSMeasurement precision

Solution Approach 1:

The patent applies parameter changes by transforming the cytometric data through scaling operations. Specifically, it scales the data based on the coefficient of variation (CV) of each parameter, converting raw values into standardized scores that account for the variability inherent in high-dimensional measurements. This transformation changes the parameter representation from raw intensity values to scaled scores, thereby improving signal-to-noise ratio while preserving the high dimensionality information.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces an additional dimensional transformation by adding a scaled score dimension to the existing high-dimensional cytometric data. Each parameter is enhanced with a scaled score that represents its signal-to-noise characteristics, creating an extended feature space that maintains the original dimensional information while adding discriminative power for noise reduction.

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

2Ease of operation

If conventional scaling methods are applied to cytometric data, then data normalization is achieved, but signal-to-noise characteristics are not optimized

Engineering Contradiction:
Improvedata normalizationVSAvoidsignal-to-noise characteristics
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The patent improves upon conventional normalization by changing the scaling parameter from simple min-max or z-score normalization to CV-based scaling. The scaling factor is derived from the coefficient of variation (standard deviation divided by mean) of each parameter, which captures the relative variability specific to cytometric measurements. This parameter change optimizes the scaling to reflect the actual signal-to-noise characteristics of the data.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent incorporates feedback mechanisms by using the observed distribution characteristics (mean and standard deviation) of each parameter to dynamically adjust the scaling factor. The scaling process uses feedback from the data itself - parameters with higher variability receive different scaling treatment than those with lower variability, creating an adaptive normalization that optimizes signal-to-noise ratio based on the actual data characteristics.

Inventive Principle:
Principle #23Feedback

Data Source

PatentUS12306087B2Method for optimal scaling of cytometry data for machine learning analysis and systems for same
Publication Date: 2025.05.20 BECTON DICKINSON & CO
  • US12306087B2 patent drawing
  • US12306087B2 patent drawing
  • US12306087B2 patent drawing

AI summary

Aspects of the present disclosure include methods for processing and scaling cytometric data. Methods according to certain embodiments include obtaining cytometric data for a sample, wherein the cytometric data comprises measurements of a plurality of parameters from particles irradiated in the sample flowing in a flow stream; identifying a parameter of interest; specifying positive and negative measurement intervals on the parameter of interest; scaling the cytometric data by transforming the parameter of interest based at least in part on the corresponding specified positive and negative intervals. Systems for practicing the subject methods are also provided. Non-transitory computer readable storage mediums are also described.