General Dimensional Multiple-Output Support Vector Regressions and Their Multiple Kernel Learning

2015 ◽  
Vol 45 (11) ◽  
pp. 2572-2584 ◽  
Author(s):  
Wooyong Chung ◽  
Jisu Kim ◽  
Heejin Lee ◽  
Euntai Kim
2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Wenjia Niu ◽  
Kewen Xia ◽  
Baokai Zu ◽  
Jianchuan Bai

Unlike Support Vector Machine (SVM), Multiple Kernel Learning (MKL) allows datasets to be free to choose the useful kernels based on their distribution characteristics rather than a precise one. It has been shown in the literature that MKL holds superior recognition accuracy compared with SVM, however, at the expense of time consuming computations. This creates analytical and computational difficulties in solving MKL algorithms. To overcome this issue, we first develop a novel kernel approximation approach for MKL and then propose an efficient Low-Rank MKL (LR-MKL) algorithm by using the Low-Rank Representation (LRR). It is well-acknowledged that LRR can reduce dimension while retaining the data features under a global low-rank constraint. Furthermore, we redesign the binary-class MKL as the multiclass MKL based on pairwise strategy. Finally, the recognition effect and efficiency of LR-MKL are verified on the datasets Yale, ORL, LSVT, and Digit. Experimental results show that the proposed LR-MKL algorithm is an efficient kernel weights allocation method in MKL and boosts the performance of MKL largely.


2018 ◽  
Vol 2018 ◽  
pp. 1-15 ◽  
Author(s):  
Hong Zheng ◽  
Haibin Li ◽  
Xingjian Lu ◽  
Tong Ruan

Air quality prediction is an important research issue due to the increasing impact of air pollution on the urban environment. However, existing methods often fail to forecast high-polluting air conditions, which is precisely what should be highlighted. In this paper, a novel multiple kernel learning (MKL) model that embodies the characteristics of ensemble learning, kernel learning, and representative learning is proposed to forecast the near future air quality (AQ). The centered alignment approach is used for learning kernels, and a boosting approach is used to determine the proper number of kernels. To demonstrate the performance of the proposed MKL model, its performance is compared to that of classical autoregressive integrated moving average (ARIMA) model; widely used parametric models like random forest (RF) and support vector machine (SVM); popular neural network models like multiple layer perceptron (MLP); and long short-term memory neural network. Datasets acquired from a coastal city Hong Kong and an inland city Beijing are used to train and validate all the models. Experiments show that the MKL model outperforms the other models. Moreover, the MKL model has better forecast ability for high health risk category AQ.


Author(s):  
Ren Qi ◽  
Jin Wu ◽  
Fei Guo ◽  
Lei Xu ◽  
Quan Zou

Abstract Single-cell RNA-sequencing (scRNA-seq) data widely exist in bioinformatics. It is crucial to devise a distance metric for scRNA-seq data. Almost all existing clustering methods based on spectral clustering algorithms work in three separate steps: similarity graph construction; continuous labels learning; discretization of the learned labels by k-means clustering. However, this common practice has potential flaws that may lead to severe information loss and degradation of performance. Furthermore, the performance of a kernel method is largely determined by the selected kernel; a self-weighted multiple kernel learning model can help choose the most suitable kernel for scRNA-seq data. To this end, we propose to automatically learn similarity information from data. We present a new clustering method in the form of a multiple kernel combination that can directly discover groupings in scRNA-seq data. The main proposition is that automatically learned similarity information from scRNA-seq data is used to transform the candidate solution into a new solution that better approximates the discrete one. The proposed model can be efficiently solved by the standard support vector machine (SVM) solvers. Experiments on benchmark scRNA-Seq data validate the superior performance of the proposed model. Spectral clustering with multiple kernels is implemented in Matlab, licensed under Massachusetts Institute of Technology (MIT) and freely available from the Github website, https://github.com/Cuteu/SMSC/.


2019 ◽  
Vol 35 (24) ◽  
pp. 5137-5145 ◽  
Author(s):  
Onur Dereli ◽  
Ceyda Oğuz ◽  
Mehmet Gönen

Abstract Motivation Survival analysis methods that integrate pathways/gene sets into their learning model could identify molecular mechanisms that determine survival characteristics of patients. Rather than first picking the predictive pathways/gene sets from a given collection and then training a predictive model on the subset of genomic features mapped to these selected pathways/gene sets, we developed a novel machine learning algorithm (Path2Surv) that conjointly performs these two steps using multiple kernel learning. Results We extensively tested our Path2Surv algorithm on 7655 patients from 20 cancer types using cancer-specific pathway/gene set collections and gene expression profiles of these patients. Path2Surv statistically significantly outperformed survival random forest (RF) on 12 out of 20 datasets and obtained comparable predictive performance against survival support vector machine (SVM) using significantly fewer gene expression features (i.e. less than 10% of what survival RF and survival SVM used). Availability and implementation Our implementations of survival SVM and Path2Surv algorithms in R are available at https://github.com/mehmetgonen/path2surv together with the scripts that replicate the reported experiments. Supplementary information Supplementary data are available at Bioinformatics online.


Author(s):  
SHIJUN WANG ◽  
JIANHUA YAO ◽  
NICHOLAS PETRICK ◽  
RONALD M. SUMMERS

Computed tomographic colonography (CTC) combined with a computer aided detection system provides a feasible approach for improving colonic polyps detection and increasing the use of CTC for colon cancer screening. To distinguish true polyps from false positives, various features extracted from polyp candidates have been proposed. Most of these traditional features try to capture the shape information of polyp candidates or neighborhood knowledge about the surrounding structures (fold, colon wall, etc.). In this paper, we propose a new set of shape descriptors for polyp candidates based on statistical curvature information. These features called histograms of curvature features are rotation, translation and scale invariant and can be treated as complementing existing feature set. Then in order to make full use of the traditional geometric features (defined as group A) and the new statistical features (group B) which are highly heterogeneous, we employed a multiple kernel learning method based on semi-definite programming to learn an optimized classification kernel from the two groups of features. We conducted leave-one-patient-out test on a CTC dataset which contained scans from 66 patients. Experimental results show that a support vector machine (SVM) based on the combined feature set and the semi-definite optimization kernel achieved higher FROC performance compared to SVMs using the two groups of features separately.


2020 ◽  
Vol 36 (12) ◽  
pp. 3766-3772 ◽  
Author(s):  
Arezou Rahimi ◽  
Mehmet Gönen

Abstract Motivation Genomic information is increasingly being used in diagnosis, prognosis and treatment of cancer. The severity of the disease is usually measured by the tumor stage. Therefore, identifying pathways playing an important role in progression of the disease stage is of great interest. Given that there are similarities in the underlying mechanisms of different cancers, in addition to the considerable correlation in the genomic data, there is a need for machine learning methods that can take these aspects of genomic data into account. Furthermore, using machine learning for studying multiple cancer cohorts together with a collection of molecular pathways creates an opportunity for knowledge extraction. Results We studied the problem of discriminating early- and late-stage tumors of several cancers using genomic information while enforcing interpretability on the solutions. To this end, we developed a multitask multiple kernel learning (MTMKL) method with a co-clustering step based on a cutting-plane algorithm to identify the relationships between the input tasks and kernels. We tested our algorithm on 15 cancer cohorts and observed that, in most cases, MTMKL outperforms other algorithms (including random forests, support vector machine and single-task multiple kernel learning) in terms of predictive power. Using the aggregate results from multiple replications, we also derived similarity matrices between cancer cohorts, which are, in many cases, in agreement with available relationships reported in the relevant literature. Availability and implementation Our implementations of support vector machine and multiple kernel learning algorithms in R are available at https://github.com/arezourahimi/mtgsbc together with the scripts that replicate the reported experiments. Supplementary information Supplementary data are available at Bioinformatics online.


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