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matlab software based pca  (MathWorks Inc)


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    MathWorks Inc matlab software based pca
    Matlab Software Based Pca, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 93/100, based on 76 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/matlab-based+pca/MATLAB+Parallel+Server/pm36825770-99-11-11
    Average 93 stars, based on 76 article reviews
    matlab software based pca - by Bioz Stars, 2026-10
    93/100 stars

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    other:

    Article Title: Application of weighted centroid algorithm based on weight correction in node localization of wireless sensor networks
    Article Snippet: The computer operating system was Windows 10 Pro 64 bit, the CPU was Intel Core i7-10700 K @ 3.8 GHz, and supported MATLAB parallel computing.

    Article Title: Application of weighted centroid algorithm based on weight correction in node localization of wireless sensor networks.
    Article Snippet: The computer operating system was Windows 10 Pro 64 bit, the CPU was Intel Core i7-10700 K @ 3.8 GHz, and supported MATLAB parallel computing.

    Blocking Assay:

    Article Title: Remote Real-Time Monitoring and Control of Small Wind Turbines Using Open-Source Hardware and Software
    Article Snippet: .. Algorithm 1: Pseudocode—Process Management and Communication Logic maestro.py (Process Manager) ---------------------- Define list of subprocesses: [process1.py, process2.py] For each process in list: -Create a new worker process -Assign target: run process as Python script Start all worker processes in parallel Wait for processes to run continuously (blocking) process1.py (Measurement Data Server) ------------------------------- Initialize UART port (9600 bps, timeout 2.5 s) Start WebSocket server on port 8081 On client connection: Loop indefinitely: -Read up to 32 bytes from UART buffer -If more data is available: -Read remaining bytes (in waiting) -Concatenate full message -Send raw data to client via WebSocket -Wait for client acknowledgment before next cycle process2.py (Control Command Server) ------------------------------- Start WebSocket server on port 8080 On client connection: Loop indefinitely: -Wait for command from client via WebSocket -Convert string command to ASCII bytes -Open UART port (9600 bps) -Send command to Arduino® -Send confirmation back to client Under normal conditions, the total system latency—from signal acquisition on the Arduino® to data visualization on the MATLAB® app—remains under 200 ms, supporting effective real-time control. ..

    Control:

    Article Title: Remote Real-Time Monitoring and Control of Small Wind Turbines Using Open-Source Hardware and Software
    Article Snippet: .. Algorithm 1: Pseudocode—Process Management and Communication Logic maestro.py (Process Manager) ---------------------- Define list of subprocesses: [process1.py, process2.py] For each process in list: -Create a new worker process -Assign target: run process as Python script Start all worker processes in parallel Wait for processes to run continuously (blocking) process1.py (Measurement Data Server) ------------------------------- Initialize UART port (9600 bps, timeout 2.5 s) Start WebSocket server on port 8081 On client connection: Loop indefinitely: -Read up to 32 bytes from UART buffer -If more data is available: -Read remaining bytes (in waiting) -Concatenate full message -Send raw data to client via WebSocket -Wait for client acknowledgment before next cycle process2.py (Control Command Server) ------------------------------- Start WebSocket server on port 8080 On client connection: Loop indefinitely: -Wait for command from client via WebSocket -Convert string command to ASCII bytes -Open UART port (9600 bps) -Send command to Arduino® -Send confirmation back to client Under normal conditions, the total system latency—from signal acquisition on the Arduino® to data visualization on the MATLAB® app—remains under 200 ms, supporting effective real-time control. ..

    Software:

    Article Title: A Proxy-guided Workflow for Virtual Population Development.
    Article Snippet: .. Our software runs on a cluster using MATLAB Parallel Server (MPS) on MATLAB R2024a. ..



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    MathWorks Inc matlab-based principal component analysis (pca)
    Decoding of cell marker compositions <t>during</t> <t>DAD</t> progression . (A-C) Zoomed-in micrographs of diffuse alveolar damage (DAD) patterns, as viewed by traditional H&E staining and corresponding multiplex immunohistochemistry. Panels A-C show paired H&E and multiplex images and typical patterns during exudative, intermediate, and advanced DAD, respectively. (D-E) Quantitative data on the density of immune cells (D) and structural cell markers (E) across the DAD patterns. The data are from marker density analysis in 95 multiplex-stained tissue regions of interest (ROIs) that were selected from H&E-stained sections with the criteria of having a uniform and distinct DAD histopathology. Statistical comparisons were determined by a non-parametric Kruskal–Wallis test, followed by Bonferroni post-hoc test. (F) Multivariate analysis of individual DAD region marker content and identification of 3 clusters of marker constellations by principal component analysis <t>(PCA)</t> and unsupervised K-mean clustering (Clusters 1-3). Individual ROIs within the PCA-defined clusters are color-coded according to previously H&E-confirmed DAD patterns. (G) Individual ROIs sorted for increasing abundance of the 4 markers that had the most statistical influence on initial cluster identification, again individual ROIs are color-coded according to DAD category. (H) Cell plots with relative marker densities across the identified clusters. Each horizontal line represents one DAD region; with its DAD category color-coding to the right. * p <0·05 and ** p <0·01.
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    Decoding of cell marker compositions <t>during</t> <t>DAD</t> progression . (A-C) Zoomed-in micrographs of diffuse alveolar damage (DAD) patterns, as viewed by traditional H&E staining and corresponding multiplex immunohistochemistry. Panels A-C show paired H&E and multiplex images and typical patterns during exudative, intermediate, and advanced DAD, respectively. (D-E) Quantitative data on the density of immune cells (D) and structural cell markers (E) across the DAD patterns. The data are from marker density analysis in 95 multiplex-stained tissue regions of interest (ROIs) that were selected from H&E-stained sections with the criteria of having a uniform and distinct DAD histopathology. Statistical comparisons were determined by a non-parametric Kruskal–Wallis test, followed by Bonferroni post-hoc test. (F) Multivariate analysis of individual DAD region marker content and identification of 3 clusters of marker constellations by principal component analysis <t>(PCA)</t> and unsupervised K-mean clustering (Clusters 1-3). Individual ROIs within the PCA-defined clusters are color-coded according to previously H&E-confirmed DAD patterns. (G) Individual ROIs sorted for increasing abundance of the 4 markers that had the most statistical influence on initial cluster identification, again individual ROIs are color-coded according to DAD category. (H) Cell plots with relative marker densities across the identified clusters. Each horizontal line represents one DAD region; with its DAD category color-coding to the right. * p <0·05 and ** p <0·01.
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    Decoding of cell marker compositions during DAD progression . (A-C) Zoomed-in micrographs of diffuse alveolar damage (DAD) patterns, as viewed by traditional H&E staining and corresponding multiplex immunohistochemistry. Panels A-C show paired H&E and multiplex images and typical patterns during exudative, intermediate, and advanced DAD, respectively. (D-E) Quantitative data on the density of immune cells (D) and structural cell markers (E) across the DAD patterns. The data are from marker density analysis in 95 multiplex-stained tissue regions of interest (ROIs) that were selected from H&E-stained sections with the criteria of having a uniform and distinct DAD histopathology. Statistical comparisons were determined by a non-parametric Kruskal–Wallis test, followed by Bonferroni post-hoc test. (F) Multivariate analysis of individual DAD region marker content and identification of 3 clusters of marker constellations by principal component analysis (PCA) and unsupervised K-mean clustering (Clusters 1-3). Individual ROIs within the PCA-defined clusters are color-coded according to previously H&E-confirmed DAD patterns. (G) Individual ROIs sorted for increasing abundance of the 4 markers that had the most statistical influence on initial cluster identification, again individual ROIs are color-coded according to DAD category. (H) Cell plots with relative marker densities across the identified clusters. Each horizontal line represents one DAD region; with its DAD category color-coding to the right. * p <0·05 and ** p <0·01.

    Journal: eBioMedicine

    Article Title: Diffuse alveolar damage patterns reflect the immunological and molecular heterogeneity in fatal COVID-19

    doi: 10.1016/j.ebiom.2022.104229

    Figure Lengend Snippet: Decoding of cell marker compositions during DAD progression . (A-C) Zoomed-in micrographs of diffuse alveolar damage (DAD) patterns, as viewed by traditional H&E staining and corresponding multiplex immunohistochemistry. Panels A-C show paired H&E and multiplex images and typical patterns during exudative, intermediate, and advanced DAD, respectively. (D-E) Quantitative data on the density of immune cells (D) and structural cell markers (E) across the DAD patterns. The data are from marker density analysis in 95 multiplex-stained tissue regions of interest (ROIs) that were selected from H&E-stained sections with the criteria of having a uniform and distinct DAD histopathology. Statistical comparisons were determined by a non-parametric Kruskal–Wallis test, followed by Bonferroni post-hoc test. (F) Multivariate analysis of individual DAD region marker content and identification of 3 clusters of marker constellations by principal component analysis (PCA) and unsupervised K-mean clustering (Clusters 1-3). Individual ROIs within the PCA-defined clusters are color-coded according to previously H&E-confirmed DAD patterns. (G) Individual ROIs sorted for increasing abundance of the 4 markers that had the most statistical influence on initial cluster identification, again individual ROIs are color-coded according to DAD category. (H) Cell plots with relative marker densities across the identified clusters. Each horizontal line represents one DAD region; with its DAD category color-coding to the right. * p <0·05 and ** p <0·01.

    Article Snippet: The generated DAD ROI data were subjected to multivariate analysis using a MATLAB-based principal component analysis (PCA) and K-means exploration to identify cluster formation in the PCA plot.

    Techniques: Marker, Staining, Multiplex Assay, Immunohistochemistry, Histopathology