Indoor Crowd Counting by Mixture of Gaussians Label Distribution Learning.
Ling Miaogen,Geng Xin
IEEE transactions on image processing : a publication of the IEEE Signal Processing Society
In this paper, we tackle the problem of crowd counting in indoor videos, where people often stay almost static for a long time. The label distribution, which covers a certain number of crowd counting labels, representing the degree to which each label describes the video frame, is previously adopted to model the label ambiguity of the crowd number. However, since the label ambiguity is significantly affected by the crowd number of the scene, we initialize the label distribution of each frame by the discretized Gaussian distribution with adaptive variance instead of the original single static Gaussian distribution. Moreover, considering the gradual change of crowd numbers in the adjacent frames, a mixture of Gaussian models is proposed to generate the final label distribution representation for each frame. The weights of the Gaussian models rely on the frame and feature distances between the current frame and the adjacent frames. The mixed l -norm is adopted to restrict the weights of predicting the adjacent crowd numbers to be locally correlated. We collect three new indoor video datasets with frame number annotation for further research. The proposed approach achieves state-of-the-art performance on seven challenging indoor videos and cross-scene experiments.
10.1109/TIP.2019.2922818
Data-Dependent Label Distribution Learning for Age Estimation.
He Zhouzhou,Li Xi,Zhang Zhongfei,Wu Fei,Geng Xin,Zhang Yaqing,Yang Ming-Hsuan,Zhuang Yueting
IEEE transactions on image processing : a publication of the IEEE Signal Processing Society
As an important and challenging problem in computer vision, face age estimation is typically cast as a classification or regression problem over a set of face samples with respect to several ordinal age labels, which have intrinsically cross-age correlations across adjacent age dimensions. As a result, such correlations usually lead to the age label ambiguities of the face samples. Namely, each face sample is associated with a latent label distribution that encodes the cross-age correlation information on label ambiguities. Motivated by this observation, we propose a totally data-driven label distribution learning approach to adaptively learn the latent label distributions. The proposed approach is capable of effectively discovering the intrinsic age distribution patterns for cross-age correlation analysis on the basis of the local context structures of face samples. Without any prior assumptions on the forms of label distribution learning, our approach is able to flexibly model the sample-specific context aware label distribution properties by solving a multi-task problem, which jointly optimizes the tasks of age-label distribution learning and age prediction for individuals. Experimental results demonstrate the effectiveness of our approach.
10.1109/TIP.2017.2655445
A Novel Method to Detect Functional microRNA Regulatory Modules by Bicliques Merging.
Liang Cheng,Li Yue,Luo Jiawei
IEEE/ACM transactions on computational biology and bioinformatics
UNLABELLED:MicroRNAs (miRNAs) are post-transcriptional regulators that repress the expression of their targets. They are known to work cooperatively with genes and play important roles in numerous cellular processes. Identification of miRNA regulatory modules (MRMs) would aid deciphering the combinatorial effects derived from the many-to-many regulatory relationships in complex cellular systems. Here, we develop an effective method called BiCliques Merging (BCM) to predict MRMs based on bicliques merging. By integrating the miRNA/mRNA expression profiles from The Cancer Genome Atlas (TCGA) with the computational target predictions, we construct a weighted miRNA regulatory network for module discovery. The maximal bicliques detected in the network are statistically evaluated and filtered accordingly. We then employed a greedy-based strategy to iteratively merge the remaining bicliques according to their overlaps together with edge weights and the gene-gene interactions. Comparing with existing methods on two cancer datasets from TCGA, we showed that the modules identified by our method are more densely connected and functionally enriched. Moreover, our predicted modules are more enriched for miRNA families and the miRNA-mRNA pairs within the modules are more negatively correlated. Finally, several potential prognostic modules are revealed by Kaplan-Meier survival analysis and breast cancer subtype analysis. AVAILABILITY:BCM is implemented in Java and available for download in the supplementary materials, which can be found on the Computer Society Digital Library at http://doi.ieeecomputersociety.org/10.1109/ TCBB.2015.2462370.
10.1109/TCBB.2015.2462370