350 research outputs found
Testing Measurement Invariance with Ordinal Missing Data: A Comparison of Estimators and Missing Data Techniques
Ordinal missing data are common in measurement equivalence/invariance (ME/I) testing studies. However, there is a lack of guidance on the appropriate method to deal with ordinal missing data in ME/I testing. Five methods may be used to deal with ordinal missing data in ME/I testing, including the continuous full information maximum likelihood estimation method (FIML), continuous robust FIML (rFIML), FIML with probit links (pFIML), FIML with logit links (lFIML), and mean and variance adjusted weight least squared estimation method combined with pairwise deletion (WLSMV_PD). The current study evaluates the relative performance of these methods in producing valid chi-square difference tests (Δχ2) and accurate parameter estimates. The result suggests that all methods except for WLSMV_PD can reasonably control the type I error rates of (Δχ2) tests and maintain sufficient power to detect noninvariance in most conditions. Only pFIML and lFIML yield accurate factor loading estimates and standard errors across all the conditions. Recommendations are provided to researchers based on the results
A Comprehensive Python Library for Deep Learning-Based Event Detection in Multivariate Time Series Data and Information Retrieval in NLP
Event detection in time series data is crucial in various domains, including
finance, healthcare, cybersecurity, and science. Accurately identifying events
in time series data is vital for making informed decisions, detecting
anomalies, and predicting future trends. Despite extensive research exploring
diverse methods for event detection in time series, with deep learning
approaches being among the most advanced, there is still room for improvement
and innovation in this field. In this paper, we present a new deep learning
supervised method for detecting events in multivariate time series data. Our
method combines four distinct novelties compared to existing deep-learning
supervised methods. Firstly, it is based on regression instead of binary
classification. Secondly, it does not require labeled datasets where each point
is labeled; instead, it only requires reference events defined as time points
or intervals of time. Thirdly, it is designed to be robust by using a stacked
ensemble learning meta-model that combines deep learning models, ranging from
classic feed-forward neural networks (FFNs) to state-of-the-art architectures
like transformers. This ensemble approach can mitigate individual model
weaknesses and biases, resulting in more robust predictions. Finally, to
facilitate practical implementation, we have developed a Python package to
accompany our proposed method. The package, called eventdetector-ts, can be
installed through the Python Package Index (PyPI). In this paper, we present
our method and provide a comprehensive guide on the usage of the package. We
showcase its versatility and effectiveness through different real-world use
cases from natural language processing (NLP) to financial security domains.Comment: 2023 International Conference on Machine Learning and Applications
(ICMLA
Event Detection in Time Series: Universal Deep Learning Approach
Event detection in time series is a challenging task due to the prevalence of
imbalanced datasets, rare events, and time interval-defined events. Traditional
supervised deep learning methods primarily employ binary classification, where
each time step is assigned a binary label indicating the presence or absence of
an event. However, these methods struggle to handle these specific scenarios
effectively. To address these limitations, we propose a novel supervised
regression-based deep learning approach that offers several advantages over
classification-based methods. Our approach, with a limited number of
parameters, can effectively handle various types of events within a unified
framework, including rare events and imbalanced datasets. We provide
theoretical justifications for its universality and precision and demonstrate
its superior performance across diverse domains, particularly for rare events
and imbalanced datasets.Comment: To be submitted to ICML 202
Nonlinear dynamics of waves and modulated waves in 1D thermocapillary flows. I: General presentation and periodic solutions
We present experimental results on hydrothermal traveling-waves dynamics in
long and narrow 1D channels. The onset of primary traveling-wave patterns is
briefly presented for different fluid heights and for annular or bounded
channels, i.e., within periodic or non-periodic boundary conditions. For
periodic boundary conditions, by increasing the control parameter or changing
the discrete mean-wavenumber of the waves, we produce modulated waves patterns.
These patterns range from stable periodic phase-solutions, due to supercritical
Eckhaus instability, to spatio-temporal defect-chaos involving traveling holes
and/or counter-propagating-waves competition, i.e., traveling sources and
sinks. The transition from non-linearly saturated Eckhaus modulations to
transient pattern-breaks by traveling holes and spatio-temporal defects is
documented. Our observations are presented in the framework of coupled complex
Ginzburg-Landau equations with additional fourth and fifth order terms which
account for the reflection symmetry breaking at high wave-amplitude far from
onset. The second part of this paper (nlin.PS/0208030) extends this study to
spatially non-periodic patterns observed in both annular and bounded channel.Comment: 45 pages, 21 figures (elsart.cls + AMS extensions). Accepted in
Physica D. See also companion paper "Nonlinear dynamics of waves and
modulated waves in 1D thermocapillary flows. II: Convective/absolute
transitions" (nlin.PS/0208030). A version with high resolution figures is
available on N.G. web pag
EB1 regulates microtubule dynamics and tubulin sheet closure in vitro.
International audienceEnd binding 1 (EB1) is a plus-end-tracking protein (+TIP) that localizes to microtubule plus ends where it modulates their dynamics and interactions with intracellular organelles. Although the regulating activity of EB1 on microtubule dynamics has been studied in cells and purified systems, the molecular mechanisms involved in its specific activity are still unclear. Here, we describe how EB1 regulates the dynamics and structure of microtubules assembled from pure tubulin. We found that EB1 stimulates spontaneous nucleation and growth of microtubules, and promotes both catastrophes (transitions from growth to shrinkage) and rescues (reverse events). Electron cryomicroscopy showed that EB1 induces the initial formation of tubulin sheets, which rapidly close into the common 13-protofilament-microtubule architecture. Our results suggest that EB1 favours the lateral association of free tubulin at microtubule-sheet edges, thereby stimulating nucleation, sheet growth and closure. The reduction of sheet length at microtubule growing-ends together with the elimination of stressed microtubule lattices may account for catastrophes. Conversely, occasional binding of EB1 to the microtubule lattice may induce rescues
Capability of Neutrophils to Form NETs Is Not Directly Influenced by a CMA-Targeting Peptide
During inflammatory reaction, neutrophils exhibit numerous cellular and immunological functions, notably the formation of neutrophil extracellular traps (NETs) and autophagy. NETs are composed of decondensed chromatin fibers coated with various antimicrobial molecules derived from neutrophil granules. NETs participate in antimicrobial defense and can also display detrimental roles and notably trigger some of the immune features of systemic lupus erythematosus (SLE) and other autoimmune diseases. Autophagy is a complex and finely regulated mechanism involved in the cell survival/death balance that may be connected to NET formation. To shed some light on the connection between autophagy and NET formation, we designed a number of experiments in human neutrophils and both in normal and lupus-prone MRL/lpr mice to determine whether the synthetic peptide P140, which is capable of selectively modulating chaperone-mediated autophagy (CMA) in lymphocytes, could alter NET formation. P140/Lupuzor™ is currently being evaluated in phase III clinical trials involving SLE patients. Overall our in vitro and in vivo studies established that P140 does not influence NET formation, cytokine/chemokine production, or CMA in neutrophils. Thus, the beneficial effect of P140/Lupuzor™ in SLE is apparently not directly related to modulation of neutrophil function
Capability of Neutrophils to Form NETs Is Not Directly Influenced by a CMA-Targeting Peptide
During inflammatory reaction, neutrophils exhibit numerous cellular and immunological functions, notably the formation of neutrophil extracellular traps (NETs) and autophagy. NETs are composed of decondensed chromatin fibers coated with various antimicrobial molecules derived from neutrophil granules. NETs participate in antimicrobial defense and can also display detrimental roles and notably trigger some of the immune features of systemic lupus erythematosus (SLE) and other autoimmune diseases. Autophagy is a complex and finely regulated mechanism involved in the cell survival/death balance that may be connected to NET formation. To shed some light on the connection between autophagy and NET formation, we designed a number of experiments in human neutrophils and both in normal and lupus-prone MRL/lpr mice to determine whether the synthetic peptide P140, which is capable of selectively modulating chaperone-mediated autophagy (CMA) in lymphocytes, could alter NET formation. P140/Lupuzor™ is currently being evaluated in phase III clinical trials involving SLE patients. Overall our in vitro and in vivo studies established that P140 does not influence NET formation, cytokine/chemokine production, or CMA in neutrophils. Thus, the beneficial effect of P140/Lupuzor™ in SLE is apparently not directly related to modulation of neutrophil function
Determinants of low bone mineral density in people with multiple sclerosis: Role of physical activity
Background
People with multiple sclerosis (PwMS) have reduced bone mineral density (BMD), but the causes are unclear. Some factors that may cause reduced BMD in PwMS have been understudied, including physical activity, inflammation, cortisol, symptomatic fatigue, and depression. The aim of this study was to investigate factors that may uniquely contribute to reduced BMD in PwMS as compared to people without MS. We hypothesized that physical activity would be the primary determinant of low BMD in PwMS, with additional contributions from inflammation and sympathetic nervous system activation. Methods
We tested 23 PwMS (16 women; median EDSS: 2) and 22 control participants (16 women). BMD was measured from the femoral neck and lumbar spine with dual x-ray absorptiometry. Disability was measured with the Expanded Disability Status Scale, and functional capacity was measured with the Multiple Sclerosis Functional Composite. Questionnaires measured symptomatic fatigue and depression. A blood draw was used to measure calcium, phosphate, vitamin D, N-terminal telopeptide, osteopontin, and cytokine markers of inflammation. Physical activity was measured with accelerometry. Salivary cortisol and cardiac heart rate variability also were obtained. All outcome variables were compared between groups with independent samples t-tests. Variables that were different between groups and significantly correlated (Pearson product-moment) with femoral neck BMD, were included in a theoretical model to explain femoral neck BMD. The expected direction of relations in the theoretical model were developed based upon the results of previous research. A Bayesian path analysis was used to test the relations of predictive variables with femoral neck BMD and interrelations among predictive variables, as detailed in the theoretical model. Results
PwMS had lower BMD at the femoral neck than controls (p = =0.04; mean difference: -0.09; 95% CI: -0.2, -0.004; Cohen\u27s d = =0.65), and there was a smaller, statistically non-significant difference in BMD at the lumbar spine (p = =0.07; mean difference: -0.08; 95% CI: -0.17, 0.007; Cohen\u27s d = =0.59). PwMS also had lower functional capacity (p ≤ 0.001; Cohen\u27s d = =1.50), greater fatigue (pd = =1.88), greater depression (pd = =1.31), and decreased physical activity (p = =0.03; Cohen\u27s d = =0.62). Using path analysis to test our theoretical model, we found that disability (standardized estimate= -0.17), physical activity (standardized estimate=0.39), symptomatic fatigue (standardized estimate= -0.36), depression (standardized estimate= -0.30), and inflammatory markers (standardized estimate=0.27) explained 51% of the variance in femoral neck BMD. Inflammatory markers were also predictive of disability (standardized estimate=0.44) and physical activity (standardized estimate= -0.40). Symptomatic fatigue and depression were correlated (r = =0.64). Conclusion
Physical activity, symptomatic fatigue, depression, disability, and inflammation all contributed independently to decreased femoral neck BMD in PWMS. Bone metabolism in PwMS is complex. Efforts to increase physical activity and address symptomatic fatigue and depression may improve bone mineral density in PwMS. Future research should investigate the mechanisms through which symptomatic fatigue and depression contribute to reduced BMD in PwMS
Capability of Neutrophils to Form NETs Is Not Directly Influenced by a CMA-Targeting Peptide
During inflammatory reaction, neutrophils exhibit numerous cellular and immunological functions, notably the formation of neutrophil extracellular traps (NETs) and autophagy. NETs are composed of decondensed chromatin fibers coated with various antimicrobial molecules derived from neutrophil granules. NETs participate in antimicrobial defense and can also display detrimental roles and notably trigger some of the immune features of systemic lupus erythematosus (SLE) and other autoimmune diseases. Autophagy is a complex and finely regulated mechanism involved in the cell survival/death balance that may be connected to NET formation. To shed some light on the connection between autophagy and NET formation, we designed a number of experiments in human neutrophils and both in normal and lupus-prone MRL/lpr mice to determine whether the synthetic peptide P140, which is capable of selectively modulating chaperone-mediated autophagy (CMA) in lymphocytes, could alter NET formation. P140/Lupuzor™ is currently being evaluated in phase III clinical trials involving SLE patients. Overall our in vitro and in vivo studies established that P140 does not influence NET formation, cytokine/chemokine production, or CMA in neutrophils. Thus, the beneficial effect of P140/Lupuzor™ in SLE is apparently not directly related to modulation of neutrophil function
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