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Träfflista för sökning "WFRF:(Wu Yanan) srt2:(2015-2019)"

Sökning: WFRF:(Wu Yanan) > (2015-2019)

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1.
  • Kristanl, Matej, et al. (författare)
  • The Seventh Visual Object Tracking VOT2019 Challenge Results
  • 2019
  • Ingår i: 2019 IEEE/CVF INTERNATIONAL CONFERENCE ON COMPUTER VISION WORKSHOPS (ICCVW). - : IEEE COMPUTER SOC. - 9781728150239 ; , s. 2206-2241
  • Konferensbidrag (refereegranskat)abstract
    • The Visual Object Tracking challenge VOT2019 is the seventh annual tracker benchmarking activity organized by the VOT initiative. Results of 81 trackers are presented; many are state-of-the-art trackers published at major computer vision conferences or in journals in the recent years. The evaluation included the standard VOT and other popular methodologies for short-term tracking analysis as well as the standard VOT methodology for long-term tracking analysis. The VOT2019 challenge was composed of five challenges focusing on different tracking domains: (i) VOT-ST2019 challenge focused on short-term tracking in RGB, (ii) VOT-RT2019 challenge focused on "real-time" short-term tracking in RGB, (iii) VOT-LT2019 focused on long-term tracking namely coping with target disappearance and reappearance. Two new challenges have been introduced: (iv) VOT-RGBT2019 challenge focused on short-term tracking in RGB and thermal imagery and (v) VOT-RGBD2019 challenge focused on long-term tracking in RGB and depth imagery. The VOT-ST2019, VOT-RT2019 and VOT-LT2019 datasets were refreshed while new datasets were introduced for VOT-RGBT2019 and VOT-RGBD2019. The VOT toolkit has been updated to support both standard short-term, long-term tracking and tracking with multi-channel imagery. Performance of the tested trackers typically by far exceeds standard baselines. The source code for most of the trackers is publicly available from the VOT page. The dataset, the evaluation kit and the results are publicly available at the challenge website(1).
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2.
  • Wu, Yunzhen, et al. (författare)
  • Orienting Active Crystal Planes of New Class Lacunaris Fe2PO5 Polyhedrons for Robust Water Oxidation in Alkaline and Neutral Media
  • 2018
  • Ingår i: Advanced Functional Materials. - : Wiley-VCH Verlagsgesellschaft. - 1616-301X .- 1616-3028. ; 28:35
  • Tidskriftsartikel (refereegranskat)abstract
    • Developing efficient and stable oxygen evolution reaction (OER) electrocatalysts is essential for realizing sustainable energy conversion, such as solar fuels. Although modulating active sites and electron transfer is of great significance to boost electrocatalysis activity, it still remains a big challenge to desirably actualize this goal. Herein, engineering of active sites and electronic framework is implemented via oriented modulation of crystal planes and construction of lacunaris architecture supported by ammonification-elicited simultaneous incorporation of nitrogen and oxygen-defect strategy. The new class porous nitrogen-incorporated Fe2PO5 with oxygen-defect (N-Fe2PO5-x) polyhedron with dominantly exposed {110} reactive facets exhibits superior performance toward water oxidation, achieving current densities of 10 mA cm(-2) at quite low overpotentials of 235 and 315 mV in alkaline and neutral media, respectively. Furthermore, density functional theoretical calculations reveal the energetically favorable {110} planes of lower absorption energy of intermediates and remolding of electronic density framework arising from the ammoniated elicitation process, contributing to excellent OER performance of lacunaris N-Fe2PO5-x polyhedrons. This work may offer a feasible guideline for regulating active sites and electron transfer to develop low-cost and highly efficient OER electrocatalysts in energy conversion systems.
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3.
  • Wang, Ying, et al. (författare)
  • Screening for Differentially Expressed Circular RNAs in the Cartilage of Osteoarthritis Patients for Their Diagnostic Value
  • 2019
  • Ingår i: Genetic Testing and Molecular Biomarkers. - : Mary Ann Liebert. - 1945-0265 .- 1945-0257. ; 23:10, s. 706-716
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Osteoarthritis (OA) is the most prevalent osteoarticular disease, which typically involves chronic cartilage degeneration and synovitis. The latest research shows that circular RNAs (circRNAs) play a role in the development of a variety of diseases, including osteoarthrosis.Purposes: The aim of this study was to explore the expression of circRNAs in OA chondrocytes and predict biomarkers for diagnosis.Materials and Methods: The circRNA expression profile was analyzed through use of the Gene Spring software V13.0; differentially expressed circRNAs were screened by comparing OA chondrocytes and normal articular chondrocytes. We validated the microarray data by quantitative real-time polymerase chain reaction analyses of OA chondrocytes and chondrocytes from normal controls. TargetScan software and miRanda software were used to predict networks of circRNA–miRNA interactions in cartilage. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and Gene Ontology (GO) analyses were applied to predict the functions of differentially expressed circRNAs.Results: Overall, 1380 circRNAs were differentially expressed between OA chondrocytes and normal articular chondrocytes (fold-change ≥2, p ≤ 0.05), including 215 that were upregulated and 1165 that were downregulated circRNAs. After analyzing the differentially expressed circRNA genes, the top 20 enriched GO entries and KEGG pathways were annotated. The hsa_circrna_0032131 was identified for further analysis. A circRNA–miRNA network was constructed to represent the 10 most likely target genes associated with the validated circRNA.Conclusions: Our research suggests that some of the differentially expressed circRNAs in OA chondrocytes compared to normal chondrocytes are etiologically associated with the pathological process of OA. It was found that hsa_circRNA_0032131 likely participates in the initiation and progression of OA and has potential as a diagnostic marker.Clinical Relevance: To analyze the difference of circRNA expression profiles between OA and normal controls and explore biomarkers for diagnosis.
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4.
  • Wu, Jian, et al. (författare)
  • Base-Station Sleeping Control and Power Matching for Energy–Delay Tradeoffs With Bursty Traffic
  • 2016
  • Ingår i: IEEE Transactions on Vehicular Technology. - : IEEE Press. - 0018-9545 .- 1939-9359.
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper, we study sleeping control (SC) and power matching (PM) for a single cell in cellular networks with bursty traffic. The base station (BS) sleeps whenever the system is empty and wakes up when N users are assembled during the sleep period. The service capacity of the BS in the active mode is controlled by adjusting its transmit power. The total power consumption and average delay are analyzed, and based on this, the impact of parameter N and transmit power on the energy-delay tradeoff is studied. It is shown that, given the average traffic load, the more bursty the traffic is, the less total power consumed, although the delay performance of more bursty traffic is better only under certain circumstances. The optimal energy-delay tradeoff is then obtained through joint SC and PM optimization. The relationship between the optimal control parameters and the asymptotic performance are also provided. Moreover, the influence of the traffic autocorrelation is explored, which shows less impact on the system performance compared with that of the burstiness. Numerical results show the energy saving gain of the joint SC and PM scheme, as well as the impact of burstiness on the optimal energy-delay tradeoff.
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