Automated Single Molecule Imaging System Illumination Correction
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Solution Overview
Problem
Current systems face challenges in accurately processing and analyzing large datasets of single molecule images, particularly in optical mapping, due to issues with uneven illumination and manual focusing, which hinders the extraction of meaningful data from single molecule studies.
Innovation Solution
An automated system for collecting and processing single molecule images that maintains focus, reduces uneven illumination through flattening, and automatically merges overlapping images, using techniques like Laplacian filters and Cross-Correlation Functions to ensure precise alignment and data quality.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Productivity
If automated image collection is implemented, then productivity is improved, but device complexity increases
Solution Approach 1:
The system performs automated focusing, illumination flattening, and image merging without continuous human intervention. The computer executes algorithms that autonomously process images, adjust parameters, and generate corrected outputs, enabling the system to serve itself in complex processing tasks.
Solution Approach 2:
Manual mechanical focusing and image processing are replaced with computer-based automated focusing algorithms and digital image processing software. The system uses computational methods to perform tasks that would otherwise require manual mechanical adjustment and analysis.
2Measurement precision
If manual focusing is used, then device complexity is reduced, but measurement precision deteriorates
Solution Approach 1:
Manual mechanical focusing is replaced with automated focusing algorithms executed by a computer. The system uses software-based focus determination and adjustment mechanisms that provide more precise and consistent focusing compared to manual methods.
Solution Approach 2:
The system employs feedback mechanisms where image quality metrics are continuously monitored and used to adjust focusing parameters. The computer analyzes image data and automatically adjusts focus settings to optimize image quality, creating a closed-loop control system.
3Measurement precision
If uneven illumination is not corrected, then device complexity is reduced, but measurement precision deteriorates
Solution Approach 1:
Physical illumination correction hardware is replaced with computational flattening algorithms. The computer processes image data to correct uneven illumination patterns through software-based image processing techniques, eliminating the need for additional optical components.
Solution Approach 2:
The system changes the parameters of image processing through automated parameter adjustment. The computer analyzes illumination patterns and automatically modifies processing parameters to correct uneven illumination, adapting the processing approach based on the specific characteristics of each image set.
4Loss of information
If overlapping images are not merged, then device complexity is reduced, but loss of information increases
Solution Approach 1:
The system merges overlapping images to create a comprehensive data set. Adjacent images that overlap are combined through automated processes that integrate information from multiple images, ensuring complete coverage and eliminating gaps in the data.
Solution Approach 2:
The system creates and uses copies of image data during the merging process. Original images are copied and processed to generate corrected versions, with overlapping regions being copied from multiple sources and integrated to produce a complete merged result.
Data Source
AI summary
There is provided a high throughput automated single molecule image collection and processing system that requires minimal initial user input. The unique features embodied in the present disclosure allow automated collection and initial processing of optical images of single molecules and their assemblies. Correct focus may be automatically maintained while images are collected. Uneven illumination in fluorescence microscopy is accounted for, and an overall robust imaging operation is provided yielding individual images prepared for further processing in external systems. Embodiments described herein are useful in studies of any macromolecules such as DNA, RNA, peptides and proteins. The automated image collection and processing system and method of same may be implemented and deployed over a computer network, and may be ergonomically optimized to facilitate user interaction.


