研究目的
To develop a flexible software package for visualization and analysis of single-molecule localization microscopy data to extract quantitative information from super-resolution datasets.
研究成果
SMoLR provides a versatile tool for quantitative analysis of SMLM data, enabling visualization, clustering, and feature-based alignment to study nanoscale biological structures. It complements existing software by offering batch processing and integration with the R environment, facilitating deeper insights into protein organization and biological processes.
研究不足
SMoLR is primarily designed for 2D-localization data; 3D clustering is not directly implemented. The software may require computational resources for large datasets, and its effectiveness depends on the quality and format of the input data.
1:Experimental Design and Method Selection:
The study involves the development of the SMoLR software package in the R programming environment, designed to handle SMLM data consisting of Cartesian coordinates and localization precision. Methods include importing data from various formats, visualization techniques (Gaussian plotting, 2D-KDE, scatter plots), clustering algorithms (KDE, DBSCAN, Voronoi tessellation), and particle averaging based on image features.
2:Sample Selection and Data Sources:
SMLM data from biological samples, such as proteins involved in DNA double strand break repair (e.g., RAD51 and BRCA2 in U2Os cells), are used. Data is obtained from single-molecule localization software like ThunderSTORM, Zeiss ZEN, SOSplugin, or plain text files.
3:List of Experimental Equipment and Materials:
Not specified in the paper; the focus is on software tools rather than physical equipment.
4:Experimental Procedures and Operational Workflow:
Data is extracted from microscopy images, imported into SMoLR, regions of interest (ROIs) are selected manually or automatically using ImageJ or SMoLR functions, and analyses (visualization, clustering, statistical exploration) are performed. Particle averaging involves aligning structures based on extracted features.
5:Data Analysis Methods:
Statistical analysis is conducted using R's capabilities, including functions from packages like spatstat for spatial point pattern analysis, EBImage for image features, and custom scripts for clustering and averaging.
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ThunderSTORM
Plugin for ImageJ used for PALM and STORM data analysis and super-resolution imaging.
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Zeiss ZEN software
Zeiss
Software for microscopy data acquisition and analysis.
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SOSplugin
Plugin for single-molecule localization data extraction.
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ImageJ
Open-source platform for biological-image analysis, used for ROI selection.
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Fiji
Distribution of ImageJ with bundled plugins, used for image analysis.
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spatstat
R package for spatial point pattern analysis, used for visualization and clustering.
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EBImage
R package for image processing, used for calculating image features.
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dbscan
R package for density-based clustering algorithms.
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