scholarly journals One-step Multi-view Spectral Clustering with Cluster Label Correlation Graph

Author(s):  
S. El Hajjar ◽  
F. Dornaika ◽  
F. Abdallah
2020 ◽  
Vol 135 ◽  
pp. 8-14
Author(s):  
Tao Tong ◽  
Jiangzhang Gan ◽  
Guoqiu Wen ◽  
Yangding Li
Keyword(s):  

2019 ◽  
Vol 31 (10) ◽  
pp. 2022-2034 ◽  
Author(s):  
Xiaofeng Zhu ◽  
Shichao Zhang ◽  
Wei He ◽  
Rongyao Hu ◽  
Cong Lei ◽  
...  
Keyword(s):  

Author(s):  
Feiping Nie ◽  
Jing Li ◽  
Xuelong Li

In multiview learning, it is essential to assign a reasonable weight to each view according to its importance. Thus, for multiview clustering task, a wise and elegant method should achieve clustering multiview data while learning the view weights. In this paper, we address this problem by exploring a Laplacian rank constrained graph, which can be approximately as the centroid of the built graph for each view with different confidences. We start our work with a natural thought that the weights can be learned by introducing a hyperparameter. By analyzing the weakness of it, we further propose a new multiview clustering method which is totally self-weighted. Furthermore, once the target graph is obtained in our models, we can directly assign the cluster label to each data point and do not need any postprocessing such as $K$-means in standard spectral clustering. Evaluations on two synthetic datasets prove the effectiveness of our methods. Compared with several representative graph-based multiview clustering approaches on four real-world datasets, experimental results demonstrate that the proposed methods achieve the better performances and our new clustering method is more practical to use.


2021 ◽  
Vol 11 (24) ◽  
pp. 12145
Author(s):  
Jun Huang ◽  
Qian Xu ◽  
Xiwen Qu ◽  
Yaojin Lin ◽  
Xiao Zheng

In multi-label learning, each object is represented by a single instance and is associated with more than one class labels, where the labels might be correlated with each other. As we all know, exploiting label correlations can definitely improve the performance of a multi-label classification model. Existing methods mainly model label correlations in an indirect way, i.e., adding extra constraints on the coefficients or outputs of a model based on a pre-learned label correlation graph. Meanwhile, the high dimension of the feature space also poses great challenges to multi-label learning, such as high time and memory costs. To solve the above mentioned issues, in this paper, we propose a new approach for Multi-Label Learning by Correlation Embedding, namely MLLCE, where the feature space dimension reduction and the multi-label classification are integrated into a unified framework. Specifically, we project the original high-dimensional feature space to a low-dimensional latent space by a mapping matrix. To model label correlation, we learn an embedding matrix from the pre-defined label correlation graph by graph embedding. Then, we construct a multi-label classifier from the low-dimensional latent feature space to the label space, where the embedding matrix is utilized as the model coefficients. Finally, we extend the proposed method MLLCE to the nonlinear version, i.e., NL-MLLCE. The comparison experiment with the state-of-the-art approaches shows that the proposed method MLLCE has a competitive performance in multi-label learning.


Author(s):  
R.P. Goehner ◽  
W.T. Hatfield ◽  
Prakash Rao

Computer programs are now available in various laboratories for the indexing and simulation of transmission electron diffraction patterns. Although these programs address themselves to the solution of various aspects of the indexing and simulation process, the ultimate goal is to perform real time diffraction pattern analysis directly off of the imaging screen of the transmission electron microscope. The program to be described in this paper represents one step prior to real time analysis. It involves the combination of two programs, described in an earlier paper(l), into a single program for use on an interactive basis with a minicomputer. In our case, the minicomputer is an INTERDATA 70 equipped with a Tektronix 4010-1 graphical display terminal and hard copy unit.A simplified flow diagram of the combined program, written in Fortran IV, is shown in Figure 1. It consists of two programs INDEX and TEDP which index and simulate electron diffraction patterns respectively. The user has the option of choosing either the indexing or simulating aspects of the combined program.


Author(s):  
Richard D. Powell ◽  
James F. Hainfeld ◽  
Carol M. R. Halsey ◽  
David L. Spector ◽  
Shelley Kaurin ◽  
...  

Two new types of covalently linked, site-specific immunoprobes have been prepared using metal cluster labels, and used to stain components of cells. Combined fluorescein and 1.4 nm “Nanogold” labels were prepared by using the fluorescein-conjugated tris (aryl) phosphine ligand and the amino-substituted ligand in the synthesis of the Nanogold cluster. This cluster label was activated by reaction with a 60-fold excess of (sulfo-Succinimidyl-4-N-maleiniido-cyclohexane-l-carboxylate (sulfo-SMCC) at pH 7.5, separated from excess cross-linking reagent by gel filtration, and mixed in ten-fold excess with Goat Fab’ fragments against mouse IgG (obtained by reduction of F(ab’)2 fragments with 50 mM mercaptoethylamine hydrochloride). Labeled Fab’ fragments were isolated by gel filtration HPLC (Superose-12, Pharmacia). A combined Nanogold and Texas Red label was also prepared, using a Nanogold cluster derivatized with both and its protected analog: the cluster was reacted with an eight-fold excess of Texas Red sulfonyl chloride at pH 9.0, separated from excess Texas Red by gel filtration, then deprotected with HC1 in methanol to yield the amino-substituted label.


2006 ◽  
Vol 73 ◽  
pp. 85-96 ◽  
Author(s):  
Richard J. Reece ◽  
Laila Beynon ◽  
Stacey Holden ◽  
Amanda D. Hughes ◽  
Karine Rébora ◽  
...  

The recognition of changes in environmental conditions, and the ability to adapt to these changes, is essential for the viability of cells. There are numerous well characterized systems by which the presence or absence of an individual metabolite may be recognized by a cell. However, the recognition of a metabolite is just one step in a process that often results in changes in the expression of whole sets of genes required to respond to that metabolite. In higher eukaryotes, the signalling pathway between metabolite recognition and transcriptional control can be complex. Recent evidence from the relatively simple eukaryote yeast suggests that complex signalling pathways may be circumvented through the direct interaction between individual metabolites and regulators of RNA polymerase II-mediated transcription. Biochemical and structural analyses are beginning to unravel these elegant genetic control elements.


2010 ◽  
Vol 43 (18) ◽  
pp. 16
Author(s):  
MATTHEW R.G. TAYLOR
Keyword(s):  

2007 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
C.W. Kim ◽  
Y.H. Kim ◽  
H.G. Cha ◽  
D.K. Lee ◽  
Y.S. Kang

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