Dynamic Label Graph Matching for Unsupervised Video Re-identification

© 2017 IEEE. Label estimation is an important component in an unsupervised person re-identification (re-ID) system. This paper focuses on cross-camera label estimation, which can be subsequently used in feature learning to learn robust re-ID models. Specifically, we propose to construct a graph for samples in each camera, and then graph matching scheme is introduced for cross-camera labeling association. While labels directly output from existing graph matching methods may be noisy and inaccurate due to significant cross-camera variations, this paper propose a dynamic graph matching (DGM) method. DGM iteratively updates the image graph and the label estimation process by learning a better feature space with intermediate estimated labels. DGM is advantageous in two aspects: 1) the accuracy of estimated labels is improved significantly with the iterations; 2) DGM is robust to noisy initial training data. Extensive experiments conducted on three benchmarks including the large-scale MARS dataset show that DGM yields competitive performance to fully supervised baselines, and outperforms competing unsupervised learning methods.

Image-Image Domain Adaptation with Preserved Self-Similarity and Domain-Dissimilarity for Person Re-identification

© 2018 IEEE. Person re-identification (re-ID) models trained on one domain often fail to generalize well to another. In our attempt, we present a 'learning via translation' framework. In the baseline, we translate the labeled images from source to target domain in an unsupervised manner. We then train re-ID models with the translated images by supervised methods. Yet, being an essential part of this framework, unsupervised image-image translation suffers from the information loss of source-domain labels during translation. Our motivation is two-fold. First, for each image, the discriminative cues contained in its ID label should be maintained after translation. Second, given the fact that two domains have entirely different persons, a translated image should be dissimilar to any of the target IDs. To this end, we propose to preserve two types of unsupervised similarities, 1) self-similarity of an image before and after translation, and 2) domain-dissimilarity of a translated source image and a target image. Both constraints are implemented in the similarity preserving generative adversarial network (SPGAN) which consists of an Siamese network and a CycleGAN. Through domain adaptation experiment, we show that images generated by SPGAN are more suitable for domain adaptation and yield consistent and competitive re-ID accuracy on two large-scale datasets

The controlled teleportation of an arbitrary two-atom entangled state in driven cavity QED

In this paper, we propose a scheme for the controlled teleportation of an arbitrary two-atom entangled state $|\phi>_{12}=a|gg>_{12}+b|ge>_{12}+c|eg>_{12}+d|ee>_{12}$ in driven cavity QED. An arbitrary two-atom entangled state can be teleported perfectly with the help of the cooperation of the third side by constructing a three-atom GHZ entangled state as the controlled channel. This scheme does not involve apparent (or direct) Bell-state measurement and is insensitive to the cavity decay and the thermal field. The probability of the success in our scheme is 1.0.Comment: 10 page

Discovery of new selective human aldose reductase inhibitors through virtual screening multiple binding pocket conformations

Aldose reductase reduces glucose to sorbitol. It plays a key role in many of the complications arising from diabetes. Thus, aldose reductase inhibitors (ARI) have been identified as promising therapeutic agents for treating such complications of diabetes, as neuropathy, nephropathy, retinopathy, and cataracts. In this paper, a virtual screening protocol applied to a library of compounds in house has been utilized to discover novel ARIs. IC50's were determined for 15 hits that inhibited ALR2 to greater than 50% at 50 uM, and ten of these have an IC50 of 10 uM or less, corresponding to a rather substantial hit rate of 14% at this level. The specificity of these compounds relative to their cross-reactivity with human ALR1 was also assessed by inhibition assays. This resulted in identification of novel inhibitors with IC50's comparable to the commercially available drug, epalrestat, and greater than an order of magnitude better selectivity

EpiDISH web server: Epigenetic Dissection of Intra-Sample-Heterogeneity with online GUI

It is well recognized that cell-type heterogeneity hampers the interpretation of Epigenome-Wide Association Studies (EWAS). Many tools have emerged to address this issue, including several R/Bioconductor packages that infer cell-type composition. Here we present a web application for cell-type deconvolution, which offers the functionality of our EpiDISH Bioconductor/R package in a user-friendly GUI environment. Users can upload their data to infer cell-type composition and differentially methylated cytosines in individual cell-types (DMCTs) for a range of different tissues. Availability and implementation EpiDISH web server is implemented with Shiny in R, and is freely available at https://www.biosino.org/EpiDISH/