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matlab code  (MathWorks Inc)


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    MathWorks Inc matlab code
    Matlab Code, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 95/100, based on 172 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/matlab+software+r2015a/MATLAB+Coder/pm38817021-58-20-22
    Average 95 stars, based on 172 article reviews
    matlab code - by Bioz Stars, 2026-10
    95/100 stars

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    other:

    Article Title: Towards the transformation of MATLAB models into FPGA-Based hardware accelerators
    Article Snippet: The forward pass of the reference model is independently reimplemented in MATLAB scripts and in manually optimized HLS-based C + + code, while the HDL Coder workflow is used as a comparative baseline.

    Article Title: Method and system for measuring, predicting and optimizing human alertness
    Article Snippet: The algorithms for group-average and individualized predictions were written in MATLAB, translated to C with MATLAB Coder, and then compiled into a native library.

    Article Title: Predictive temperature control of electric two wheeler hub motor using gradient aware neural regulation with degradation tracking and fault tolerant multi condition torque adaptation.
    Article Snippet: All artificial neural network (ANN) models were converted into fixed-point C code using MATLAB Coder and Embedded Coder toolchains.

    Article Title: Real-time Covid-19 diagnosis on embedded IoT platforms
    Article Snippet: The trained model was converted into an embedded-compatible format using MATLAB Coder and GPU Coder, generating CUDA-accelerated code optimized for the GPU resources available on the NVIDIA Jetson platform.

    Article Title: Towards the transformation of MATLAB models into FPGA-Based hardware accelerators.
    Article Snippet: The forward pass of the reference model is independently reimplemented in MATLAB scripts and in manually optimized HLS-based C++ code, while the HDL Coder workflow is used as a comparative baseline.

    Software:

    Article Title: Towards the transformation of MATLAB models into FPGA-Based hardware accelerators.
    Article Snippet: AMD’s Vitis Model Composer, integrated as a Simulink add-on, supports rapid prototyping of FPGA-oriented systems [12]. .. Similarly, MATLAB Coder and Hardware Description Language (HDL) Coder facilitate the conversion of algorithms developed in MATLAB into C/C++ or HDL representations, thereby bridging software-oriented models with hardware-oriented implementations [13]. ..

    Article Title: Towards the transformation of MATLAB models into FPGA-Based hardware accelerators
    Article Snippet: AMD’s Vitis Model Composer, integrated as a Simulink add-on, supports rapid prototyping of FPGA-oriented systems . .. Similarly, MATLAB Coder and Hardware Description Language (HDL) Coder facilitate the conversion of algorithms developed in MATLAB into C/C + + or HDL representations, thereby bridging software-oriented models with hardware-oriented implementations . ..

    Blocking Assay:

    Article Title: Predictive temperature control of electric two wheeler hub motor using gradient aware neural regulation with degradation tracking and fault tolerant multi condition torque adaptation.
    Article Snippet: .. Once trained, the ANN model is exported as a lightweight C-code block using MATLAB CoderTM for embedded deployment. ..



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    ( a ) Droplet-like DPICs were initially formed by mixing 20 μM ATTO565-labeled p53 4M ΔTAD with 0.6 μM ATTO488-labeled Random DNA and incubating for 30 minutes at room temperature. Subsequently, Cy5-labeled p21 DNA was added at varying concentrations and incubated for an additional 120 minutes: (i) 0.15 μM; (ii) 0.225 μM; (iii) 0.3 μM; (iv) 0.45 μM; (v) 0.6 μM; (vi) 0.75 μM; (vii) 0.9 μM. Representative fluorescence images at incubation time t = 4-min and t = 120-min are shown. Independent in vitro droplet experiments were repeated three times (n = 3). ( b ) <t>Boxplot</t> of characteristic time constants τ 1 and τ 2 for p21 DNA concentrations ranging from 0.3 to 0.9 μM. N indicates the number of individual biomolecule-rich condensates analyzed under each condition. In box plots, the black line denotes the median, box edges represent the 25 th and 75 th percentiles, whiskers indicate the range excluding outliers, and outliers are shown as individual dots (•). ( c ) Phase diagram showing normalized fluorescence intensities of ATTO565-labeled p53 4M ΔTAD and ATTO488-labeled Random DNA at the center of condensates under increasing concentrations of p21 DNA (0.3, 0.45, 0.6, and 0.75 μM). Values are shown both before p21 DNA addition and at the end of Stage I. Control experiments in which Random DNA was used in place of p21 DNA are also included. Error bars indicate mean ± s.d. Green dashed lines mark the estimated binodal boundary, and purple dashed lines represent the spinodal boundary, as confirmed by our phase-field model (see – ).
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    Image Search Results


    ( a ) Droplet-like DPICs were initially formed by mixing 20 μM ATTO565-labeled p53 4M ΔTAD with 0.6 μM ATTO488-labeled Random DNA and incubating for 30 minutes at room temperature. Subsequently, Cy5-labeled p21 DNA was added at varying concentrations and incubated for an additional 120 minutes: (i) 0.15 μM; (ii) 0.225 μM; (iii) 0.3 μM; (iv) 0.45 μM; (v) 0.6 μM; (vi) 0.75 μM; (vii) 0.9 μM. Representative fluorescence images at incubation time t = 4-min and t = 120-min are shown. Independent in vitro droplet experiments were repeated three times (n = 3). ( b ) Boxplot of characteristic time constants τ 1 and τ 2 for p21 DNA concentrations ranging from 0.3 to 0.9 μM. N indicates the number of individual biomolecule-rich condensates analyzed under each condition. In box plots, the black line denotes the median, box edges represent the 25 th and 75 th percentiles, whiskers indicate the range excluding outliers, and outliers are shown as individual dots (•). ( c ) Phase diagram showing normalized fluorescence intensities of ATTO565-labeled p53 4M ΔTAD and ATTO488-labeled Random DNA at the center of condensates under increasing concentrations of p21 DNA (0.3, 0.45, 0.6, and 0.75 μM). Values are shown both before p21 DNA addition and at the end of Stage I. Control experiments in which Random DNA was used in place of p21 DNA are also included. Error bars indicate mean ± s.d. Green dashed lines mark the estimated binodal boundary, and purple dashed lines represent the spinodal boundary, as confirmed by our phase-field model (see – ).

    Journal: bioRxiv

    Article Title: Hollow condensates emerge from gelation-induced spinodal decomposition

    doi: 10.1101/2025.06.25.661497

    Figure Lengend Snippet: ( a ) Droplet-like DPICs were initially formed by mixing 20 μM ATTO565-labeled p53 4M ΔTAD with 0.6 μM ATTO488-labeled Random DNA and incubating for 30 minutes at room temperature. Subsequently, Cy5-labeled p21 DNA was added at varying concentrations and incubated for an additional 120 minutes: (i) 0.15 μM; (ii) 0.225 μM; (iii) 0.3 μM; (iv) 0.45 μM; (v) 0.6 μM; (vi) 0.75 μM; (vii) 0.9 μM. Representative fluorescence images at incubation time t = 4-min and t = 120-min are shown. Independent in vitro droplet experiments were repeated three times (n = 3). ( b ) Boxplot of characteristic time constants τ 1 and τ 2 for p21 DNA concentrations ranging from 0.3 to 0.9 μM. N indicates the number of individual biomolecule-rich condensates analyzed under each condition. In box plots, the black line denotes the median, box edges represent the 25 th and 75 th percentiles, whiskers indicate the range excluding outliers, and outliers are shown as individual dots (•). ( c ) Phase diagram showing normalized fluorescence intensities of ATTO565-labeled p53 4M ΔTAD and ATTO488-labeled Random DNA at the center of condensates under increasing concentrations of p21 DNA (0.3, 0.45, 0.6, and 0.75 μM). Values are shown both before p21 DNA addition and at the end of Stage I. Control experiments in which Random DNA was used in place of p21 DNA are also included. Error bars indicate mean ± s.d. Green dashed lines mark the estimated binodal boundary, and purple dashed lines represent the spinodal boundary, as confirmed by our phase-field model (see – ).

    Article Snippet: The function of “boxplot” in MATLAB software (R2015a, 64-bit, February 12, 2015) was used to plot the boxplots in , , and Supplementary Fig. 3.

    Techniques: Labeling, Incubation, Fluorescence, In Vitro, Control