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Eigenvector Research Inc pls toolbox 8 9 2
Pls Toolbox 8 9 2, supplied by Eigenvector Research Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pls-toolbox/pls+toolbox/pmc13164873-218-16-18
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pls toolbox 8 9 2 - by Bioz Stars, 2026-09
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Article Title: Method for assessing nitrogen nutritional status in plants by visible-to-shortwave infrared reflectance spectroscopy of carbohydrates
Article Snippet: All the data processing was applied by PLS-Toolbox (Eigenvector Research Inc., WA, USA) running under a Matlab environment version 9.3 (The Mathworks Inc., MA, USA).

Article Title: Portable Near Infrared spectrometer to predict physicochemical properties in Cape gooseberry (Physalis peruviana L.): an approach using hierarchical classification/regression modelling
Article Snippet: Cape gooseberries are highly valued for their taste, nutraceutical benefits, and health properties, earning them recognition as a superfruit.. However, these properties vary according to the ripening stage, making it important to monitor the composition of cape gooseberries throughout their maturation.. In this study, we used a portable NIR spectrometer (900–1700 nm) combined with chemometrics to predict soluble solid content (SSC), vitamin C content, and firmness.

Article Title: Prediction of total lipids and fatty acids in black soldier fly (Hermetia illucens L.) dried larvae by NIR-hyperspectral imaging and chemometrics.
Article Snippet: • NIR-HSI predicts lipid content in intact black soldier fly larvae accurately.. • Myristic acid was accurately predicted

Article Title: Modelling and numerical methods for identifying low-level adulteration in ground beef using near-infrared hyperspectral imaging (NIR-HSI).
Article Snippet: The chemometrics analysis was conducted using PLS-Toolbox (Eigenvector Research Inc, Wenatchee, USA) and MATLAB package “Classification toolbox” [17], the statistical study was conducted via MATLAB 2022a (MathWorks Inc, MA, USA).

Article Title: The role of cytochrome c in mitochondrial metabolism of human oocytes
Article Snippet: The obtained Raman data were analyzed by Cluster Analysis using the Project Plus (WITec GmbH, Germany), Origin 2018 (Origin Lab, USA) and Principal Component Analysis (PCA) analysis was performed using MATLAB (MathWorks, USA) with PLS-Toolbox (Eigenvector Research Inc., USA).

Article Title: Metabolomic signature identifies HDL and apolipoproteins as potential biomarker for systemic sclerosis with interstitial lung disease.
Article Snippet: Quantitative values obtained from Bruker’s IVDr analysis were scaled by variance and mean-centered for Principal Component Analysis (PCA) and Partial Least Square-Discriminant Analysis (PLS-DA) performed in PLS-Toolbox (Eigenvector Research Inc., Wenatchee, WA) in Matlab.

Article Title: Analysis of biodegradable films made from cassava starch and oregano essential oil using hyperspectral imaging and portable NIR spectroscopy.
Article Snippet: • NIR-HSI is an accurate alternative for estimating the percentage of oregano essential oil (OEO) in the films.. • NIR-HSI models allow the visualization of OEO distribution on the surface of the



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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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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