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1.
Ann Appl Stat ; 18(2): 1294-1318, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38682044

ABSTRACT

Neuroimaging studies often involve predicting a scalar outcome from an array of images collectively called tensor. The use of magnetic resonance imaging (MRI) provides a unique opportunity to investigate the structures of the brain. To learn the association between MRI images and human intelligence, we formulate a scalar-on-image quantile regression framework. However, the high dimensionality of the tensor makes estimating the coefficients for all elements computationally challenging. To address this, we propose a low-rank coefficient array estimation algorithm based on tensor train (TT) decomposition which we demonstrate can effectively reduce the dimensionality of the coefficient tensor to a feasible level while ensuring adequacy to the data. Our method is more stable and efficient compared to the commonly used, Canonic Polyadic rank approximation-based method. We also propose a generalized Lasso penalty on the coefficient tensor to take advantage of the spatial structure of the tensor, further reduce the dimensionality of the coefficient tensor, and improve the interpretability of the model. The consistency and asymptotic normality of the TT estimator are established under some mild conditions on the covariates and random errors in quantile regression models. The rate of convergence is obtained with regularization under the total variation penalty. Extensive numerical studies, including both synthetic and real MRI imaging data, are conducted to examine the empirical performance of the proposed method and its competitors.

2.
J Acoust Soc Am ; 153(5): 2878, 2023 May 01.
Article in English | MEDLINE | ID: mdl-37171898

ABSTRACT

The majority of reported measurements on high intensity ultrasound beams in air are below 40 kHz and performed on standing waves inside of a guide. Here, experimental characterization of high intensity progressive and divergent sound beams in air at 300 kHz are presented. Measurements in this frequency range are challenging. Accurate characterization of high intensity sound beams requires a measurement bandwidth at least ten times the beam's primary frequency, as high intensity soundwaves steepen and form shocks and, therefore, contain significant signal power at harmonic frequencies. Hence, a measurement bandwidth of at least 3 MHz is required. Calibrated measurement microphones are generally not available in this frequency range. This limitation has been overcome by using a hydrophone with a calibrated response from 250 kHz to 20 MHz. A narrowband piezoelectric transducer is used as the source in this study, and it is capable of generating tone burst waveforms centered at 300 kHz with 160 dB sound pressure level surface pressure. Cumulative wave steepening and shock formation are observed in on-axis measurements. The source's surface vibration profile is measured using a scanning laser Doppler vibrometer, and the vibration profile is imported into a numerical wide-angle Khokhlov-Zabolotskaya-Kuznetsov simulation for comparison against measured on-axis waveforms.

3.
Genet Epidemiol ; 47(3): 215-230, 2023 04.
Article in English | MEDLINE | ID: mdl-36691909

ABSTRACT

Analysis of host genetic components provides insights into the susceptibility and response to viral infection such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19). To reveal genetic determinants of susceptibility to COVID-19 related mortality, we train a deep learning model to identify groups of genetic variants and their interactions that contribute to the COVID-19 related mortality risk using the UK Biobank data (28,097 affected cases and 1656 deaths). We refer to such groups of variants as super variants. We identify 15 super variants with various levels of significance as susceptibility loci for COVID-19 mortality. Specifically, we identify a super variant (odds ratio [OR] = 1.594, p = 5.47 × 10-9 ) on Chromosome 7 that consists of the minor allele of rs76398985, rs6943608, rs2052130, 7:150989011_CT_C, rs118033050, and rs12540488. We also discover a super variant (OR = 1.353, p = 2.87 × 10-8 ) on Chromosome 5 that contains rs12517344, rs72733036, rs190052994, rs34723029, rs72734818, 5:9305797_GTA_G, and rs180899355.


Subject(s)
COVID-19 , Deep Learning , Humans , SARS-CoV-2 , Biological Specimen Banks , Models, Genetic , United Kingdom
4.
Article in English | MEDLINE | ID: mdl-35584070

ABSTRACT

We consider the problem of nonparametric classification from a high-dimensional input vector (small n large p problem). To handle the high-dimensional feature space, we propose a random projection (RP) of the feature space followed by training of a neural network (NN) on the compressed feature space. Unlike regularization techniques (lasso, ridge, etc.), which train on the full data, NNs based on compressed feature space have significantly lower computation complexity and memory storage requirements. Nonetheless, a random compression-based method is often sensitive to the choice of compression. To address this issue, we adopt a Bayesian model averaging (BMA) approach and leverage the posterior model weights to determine: 1) uncertainty under each compression and 2) intrinsic dimensionality of the feature space (the effective dimension of feature space useful for prediction). The final prediction is improved by averaging models with projected dimensions close to the intrinsic dimensionality. Furthermore, we propose a variational approach to the afore-mentioned BMA to allow for simultaneous estimation of both model weights and model-specific parameters. Since the proposed variational solution is parallelizable across compressions, it preserves the computational gain of frequentist ensemble techniques while providing the full uncertainty quantification of a Bayesian approach. We establish the asymptotic consistency of the proposed algorithm under the suitable characterization of the RPs and the prior parameters. Finally, we provide extensive numerical examples for empirical validation of the proposed method.

5.
J Alzheimers Dis ; 83(4): 1859-1875, 2021.
Article in English | MEDLINE | ID: mdl-34459391

ABSTRACT

BACKGROUND: The transition from mild cognitive impairment (MCI) to dementia is of great interest to clinical research on Alzheimer's disease and related dementias. This phenomenon also serves as a valuable data source for quantitative methodological researchers developing new approaches for classification. However, the growth of machine learning (ML) approaches for classification may falsely lead many clinical researchers to underestimate the value of logistic regression (LR), which often demonstrates classification accuracy equivalent or superior to other ML methods. Further, when faced with many potential features that could be used for classifying the transition, clinical researchers are often unaware of the relative value of different approaches for variable selection. OBJECTIVE: The present study sought to compare different methods for statistical classification and for automated and theoretically guided feature selection techniques in the context of predicting conversion from MCI to dementia. METHODS: We used data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to evaluate different influences of automated feature preselection on LR and support vector machine (SVM) classification methods, in classifying conversion from MCI to dementia. RESULTS: The present findings demonstrate how similar performance can be achieved using user-guided, clinically informed pre-selection versus algorithmic feature selection techniques. CONCLUSION: These results show that although SVM and other ML techniques are capable of relatively accurate classification, similar or higher accuracy can often be achieved by LR, mitigating SVM's necessity or value for many clinical researchers.


Subject(s)
Alzheimer Disease/classification , Cognitive Dysfunction/classification , Machine Learning , Aged , Brain/pathology , Female , Humans , Magnetic Resonance Imaging , Male , Support Vector Machine
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