functions from the matlab bioinformatics toolbox Search Results


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Figure 2. PLS-DA analysis of lipidomic data. Lipid extracts of DU145 cells treated with TNFat different times were analysed through UPLC-TOF and data was imported into <t>MATLAB</t> environment. PLS-DA scores plots of matrices containing the concentrations of the selected compounds obtained by MCR-ALS analysis on full scan data matrices in the positive ionization mode.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Contribution ratio ( % Contribution ) of MUA and <t>LFP</t> features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the <t>LFP</t> <t>frequency</t> bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.
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Image Search Results


Figure 2. PLS-DA analysis of lipidomic data. Lipid extracts of DU145 cells treated with TNFat different times were analysed through UPLC-TOF and data was imported into MATLAB environment. PLS-DA scores plots of matrices containing the concentrations of the selected compounds obtained by MCR-ALS analysis on full scan data matrices in the positive ionization mode.

Journal: Molecular bioSystems

Article Title: Epithelial-to-mesenchymal transition involves triacylglycerol accumulation in DU145 prostate cancer cells.

doi: 10.1039/c5mb00413f

Figure Lengend Snippet: Figure 2. PLS-DA analysis of lipidomic data. Lipid extracts of DU145 cells treated with TNFat different times were analysed through UPLC-TOF and data was imported into MATLAB environment. PLS-DA scores plots of matrices containing the concentrations of the selected compounds obtained by MCR-ALS analysis on full scan data matrices in the positive ionization mode.

Article Snippet: Data was imported into MATLAB environment using mzcdfread and mzcdf2peaks functions from the MATLAB Bioinformatics Toolbox.

Techniques:

Contribution ratio ( % Contribution ) of MUA and LFP features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the LFP frequency bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.

Journal: APL Bioengineering

Article Title: Degradation-aware neural imputation: Advancing decoding stability in brain machine interfaces

doi: 10.1063/5.0250296

Figure Lengend Snippet: Contribution ratio ( % Contribution ) of MUA and LFP features in predicting forelimb movement velocities along the x- and y-axes during the baseline period (recording days 1–7). (a) Contribution ratios of neural features for predicting forelimb movement velocity along the x-axis. (b) Contribution ratios of neural features for predicting forelimb movement velocity along the y-axis. Each subplot displays the % Contribution of MUA and LFP features for a specific rat ( Rat #4 , #6 , #9 , and #10 ) using the kSIR neural decoder. The contribution ratios of MUA features are shown individually for each channel (labeled 1–8), while the contribution ratios of LFP features are accumulated for each frequency band ( δ , θ , α , β , γ , and γ ′ ) across all channels. MUA features from each channel show the highest contribution in predicting both x- and y-velocity components compared to LFP power. Among the LFP frequency bands, the γ and γ ′ and exhibit higher contribution ratios, indicating their relevance in decoding forelimb movements. Data are presented as mean ± SD.

Article Snippet: Frequency-spectrum features were widely used for processing LFPs; therefore, LFP raw data were further down-sampled to a 1-kHz sampling rate and converted to power spectral density using a short-time Fourier transform with a Hanning window of 1 f m ms in length and time step of 33-ms, where f m is the minimum frequency of each LFP frequency bands (using the spectrogram function from the Signal Processing Toolbox, MATLAB R2019a, MathWorks).

Techniques: Labeling