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chemometrics toolbox pls toolbox  (MathWorks Inc)


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    MathWorks Inc chemometrics toolbox pls toolbox
    Chemometrics Toolbox Pls Toolbox, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 2340 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pls+toolbox+for/Database+Toolbox/pm41724080-106-10-17
    Average 96 stars, based on 2340 article reviews
    chemometrics toolbox pls toolbox - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Biomarker Discovery:

    Article Title: Identification of biopsychological trait markers in functional neurological disorders
    Article Snippet: We used the publicly available PLS toolbox for MATLAB ( https://github.com/FND-ResearchGroup/myPLS_SL.git ), the use of which has already been described in other studies., We conducted three individual PLSC analyses.

    Article Title: Ethanol- and trifluoroethanol-induced changes in phase states of DPPC membranes. Prodan emission-excitation fluorescence spectroscopy supported by PARAFAC analysis.
    Article Snippet: Article history: Received 9 August 2017 Received in revised form 5 October 2017 Accepted 27 October 2017 Available online 28 October 2017 It has been shown that Prodan emission-excitation fluorescence spectroscopy supported by Parallel Factor (PARAFAC) analysis is a fast, simple and sensitive method used in the study of the phase transition from the noninterdigitated gel (Lβ′) state to the interdigitated gel (LβI) phase, triggered by ethanol and 2,2,2trifluoroethanol (TFE) molecules in dipalmitoylphosphatidylcholines (DPPC) membranes.. The relative contribution of lipid phases with spectral characteristics of each pure phase component has been presented as a function of an increase in alcohol concentration.. It has been stated that both alcohol molecules can induce a formation of the LβI phase, but TFE is over six times stronger inducer of the interdigitated phase in DPPC membranes than ethanol molecules.



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    Study schematic. ( A ) Univariate associations between FC matrices <t>and</t> <t>MBI</t> diagnosis, MBI-C total score or MBI-C subdomain score were examined using separate linear regression models, with age, sex, years of education, diagnosis and total intracranial volumes included as nuisance covariates. ( B ) In parallel, <t>partial</t> <t>least</t> <t>squares</t> correlation was conducted to examine multivariate associations between residuals of FC matrices and MBI-C subdomain scores after regressing out age, sex, years of education, diagnosis and total intracranial volumes. This approach gives rise to a set of latent variables, which are linear weighted combinations of the original variables (i.e., FC and MBI-C score loadings) that have maximal covariance with each other. Individual connectome scores and MBI-C scores were then obtained by back projecting the FC and MBI-C score loadings to their original residual values. Connectome scores describe the extent to which each participant expresses the FC pattern maximally associated with the MBI-C scores, with higher connectome scores indicating greater MBI-related functional network disruptions. ( C ) Subsequently, we examined whether connectome score or MBI-C total score interacted with global amyloid SUVR and temporal meta-ROI tau SUVR to influence baseline and rate of change in global cognition and functional performance using linear regression models. MBI-C = Mild Behavioural Impairment Checklist; MBI-C = Mild Behavioural Impairment Checklist; SUVR = standardized uptake value ratio; ROI = region-of-interest; FC = functional connectivity; AD = Alzheimer’s disease; CDR = Clinical Dementia Rating; MoCA = Montreal Cognitive Assessment
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    MathWorks Inc pls toolbox solo
    Study schematic. ( A ) Univariate associations between FC matrices <t>and</t> <t>MBI</t> diagnosis, MBI-C total score or MBI-C subdomain score were examined using separate linear regression models, with age, sex, years of education, diagnosis and total intracranial volumes included as nuisance covariates. ( B ) In parallel, <t>partial</t> <t>least</t> <t>squares</t> correlation was conducted to examine multivariate associations between residuals of FC matrices and MBI-C subdomain scores after regressing out age, sex, years of education, diagnosis and total intracranial volumes. This approach gives rise to a set of latent variables, which are linear weighted combinations of the original variables (i.e., FC and MBI-C score loadings) that have maximal covariance with each other. Individual connectome scores and MBI-C scores were then obtained by back projecting the FC and MBI-C score loadings to their original residual values. Connectome scores describe the extent to which each participant expresses the FC pattern maximally associated with the MBI-C scores, with higher connectome scores indicating greater MBI-related functional network disruptions. ( C ) Subsequently, we examined whether connectome score or MBI-C total score interacted with global amyloid SUVR and temporal meta-ROI tau SUVR to influence baseline and rate of change in global cognition and functional performance using linear regression models. MBI-C = Mild Behavioural Impairment Checklist; MBI-C = Mild Behavioural Impairment Checklist; SUVR = standardized uptake value ratio; ROI = region-of-interest; FC = functional connectivity; AD = Alzheimer’s disease; CDR = Clinical Dementia Rating; MoCA = Montreal Cognitive Assessment
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    Study schematic. ( A ) Univariate associations between FC matrices and MBI diagnosis, MBI-C total score or MBI-C subdomain score were examined using separate linear regression models, with age, sex, years of education, diagnosis and total intracranial volumes included as nuisance covariates. ( B ) In parallel, partial least squares correlation was conducted to examine multivariate associations between residuals of FC matrices and MBI-C subdomain scores after regressing out age, sex, years of education, diagnosis and total intracranial volumes. This approach gives rise to a set of latent variables, which are linear weighted combinations of the original variables (i.e., FC and MBI-C score loadings) that have maximal covariance with each other. Individual connectome scores and MBI-C scores were then obtained by back projecting the FC and MBI-C score loadings to their original residual values. Connectome scores describe the extent to which each participant expresses the FC pattern maximally associated with the MBI-C scores, with higher connectome scores indicating greater MBI-related functional network disruptions. ( C ) Subsequently, we examined whether connectome score or MBI-C total score interacted with global amyloid SUVR and temporal meta-ROI tau SUVR to influence baseline and rate of change in global cognition and functional performance using linear regression models. MBI-C = Mild Behavioural Impairment Checklist; MBI-C = Mild Behavioural Impairment Checklist; SUVR = standardized uptake value ratio; ROI = region-of-interest; FC = functional connectivity; AD = Alzheimer’s disease; CDR = Clinical Dementia Rating; MoCA = Montreal Cognitive Assessment

    Journal: Alzheimer's Research & Therapy

    Article Title: Functional network phenotypes of mild behavioural impairment: cognitive effects moderated by amyloid

    doi: 10.1186/s13195-026-01980-2

    Figure Lengend Snippet: Study schematic. ( A ) Univariate associations between FC matrices and MBI diagnosis, MBI-C total score or MBI-C subdomain score were examined using separate linear regression models, with age, sex, years of education, diagnosis and total intracranial volumes included as nuisance covariates. ( B ) In parallel, partial least squares correlation was conducted to examine multivariate associations between residuals of FC matrices and MBI-C subdomain scores after regressing out age, sex, years of education, diagnosis and total intracranial volumes. This approach gives rise to a set of latent variables, which are linear weighted combinations of the original variables (i.e., FC and MBI-C score loadings) that have maximal covariance with each other. Individual connectome scores and MBI-C scores were then obtained by back projecting the FC and MBI-C score loadings to their original residual values. Connectome scores describe the extent to which each participant expresses the FC pattern maximally associated with the MBI-C scores, with higher connectome scores indicating greater MBI-related functional network disruptions. ( C ) Subsequently, we examined whether connectome score or MBI-C total score interacted with global amyloid SUVR and temporal meta-ROI tau SUVR to influence baseline and rate of change in global cognition and functional performance using linear regression models. MBI-C = Mild Behavioural Impairment Checklist; MBI-C = Mild Behavioural Impairment Checklist; SUVR = standardized uptake value ratio; ROI = region-of-interest; FC = functional connectivity; AD = Alzheimer’s disease; CDR = Clinical Dementia Rating; MoCA = Montreal Cognitive Assessment

    Article Snippet: Behaviour partial least squares correlation was then performed on the standardized FC and MBI-C subdomain score residuals using the PLS toolbox [ ] in MATLAB.

    Techniques: Biomarker Discovery, Functional Assay

    The presence and severity of MBI are associated with whole-brain FC dysfunctions. ( A ) FC matrix (left) displays significant bootstrap ratios (> 2) of functional connections corresponding to this latent variable, while bar chart (right) displays the mean correlation values between connectome scores of this latent variable and each of the MBI-C subdomain scores (error bars denote 95% bootstrapped confidence intervals). Partial least squares correlation analysis identified one significant latent variable that explained 68.0% of covariance between FC and MBI-C subdomain scores. The latent variable was characterized by high scores across all MBI-C subdomains, indicating global, rather than domain-specific effects of MBI on brain functional networks. Further, the latent variable was associated with whole-brain FC dysfunction between and within networks, particularly in the higher-order default, control and salience/ventral attention networks. ( B-C ) FC matrices display the T-scores of functional connections showing significant (uncorrected P < 0.05) associations (hot colour: positive association; cool colour: negative association) with ( B ) MBI-C total score and ( C ) MBI diagnosis. Both higher MBI-C total score and MBI positivity were associated with widespread within- and between- network FC disruptions notably in higher-order networks, recapitulating the FC dysfunction pattern observed in the partial least squares correlation analysis. MBI = Mild Behavioural Impairment; FC = functional connectivity; MBI-C = Mild Behavioural Impairment Checklist; SalVentAttn = salience/ventral attention; DorsalAttn = dorsal attention; SomMot = somatomotor; TempPar = temporoparietal

    Journal: Alzheimer's Research & Therapy

    Article Title: Functional network phenotypes of mild behavioural impairment: cognitive effects moderated by amyloid

    doi: 10.1186/s13195-026-01980-2

    Figure Lengend Snippet: The presence and severity of MBI are associated with whole-brain FC dysfunctions. ( A ) FC matrix (left) displays significant bootstrap ratios (> 2) of functional connections corresponding to this latent variable, while bar chart (right) displays the mean correlation values between connectome scores of this latent variable and each of the MBI-C subdomain scores (error bars denote 95% bootstrapped confidence intervals). Partial least squares correlation analysis identified one significant latent variable that explained 68.0% of covariance between FC and MBI-C subdomain scores. The latent variable was characterized by high scores across all MBI-C subdomains, indicating global, rather than domain-specific effects of MBI on brain functional networks. Further, the latent variable was associated with whole-brain FC dysfunction between and within networks, particularly in the higher-order default, control and salience/ventral attention networks. ( B-C ) FC matrices display the T-scores of functional connections showing significant (uncorrected P < 0.05) associations (hot colour: positive association; cool colour: negative association) with ( B ) MBI-C total score and ( C ) MBI diagnosis. Both higher MBI-C total score and MBI positivity were associated with widespread within- and between- network FC disruptions notably in higher-order networks, recapitulating the FC dysfunction pattern observed in the partial least squares correlation analysis. MBI = Mild Behavioural Impairment; FC = functional connectivity; MBI-C = Mild Behavioural Impairment Checklist; SalVentAttn = salience/ventral attention; DorsalAttn = dorsal attention; SomMot = somatomotor; TempPar = temporoparietal

    Article Snippet: Behaviour partial least squares correlation was then performed on the standardized FC and MBI-C subdomain score residuals using the PLS toolbox [ ] in MATLAB.

    Techniques: Functional Assay, Control, Biomarker Discovery