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Zhenqiang Bao,Xiaoqing Ren,Yulu Yang,Junwu Zhu,Cheng Wang,Richao Yin 보안공학연구지원센터 2015 International Journal of Hybrid Information Techno Vol.8 No.7
Since that a job usually contains several working procedures in actual production, and it’s hard to optimize the flexible collaborative planning, the flexible lot splitting and scheduling of the job simultaneously in batch production mode, a model for multi-objective integration of flexible collaborative planning and fuzzy lot-splitting scheduling is established. We take four performance indicators below which are the most common as standards to optimize the model: average delivery satisfaction, fuzzy total cost, fuzzy completion time and average credibility of job tardiness, and then a multi-objective algorithm based on the Pareto optimal is established. In this algorithm, we design the integrated coding scheme, which include collaboration chromosome, lot-splitting chromosome and scheduling chromosome, meanwhile the Pareto optimal scheme is designed. Finally, the efficiency of the model and algorithm is proved by the simulation.
Finger Vein Recognition Using Generalized Local Line Binary Pattern
( Yu Lu ),( Sook Yoon ),( Shan Juan Xie ),( Jucheng Yang ),( Zhihui Wang ),( Dong Sun Park ) 한국인터넷정보학회 2014 KSII Transactions on Internet and Information Syst Vol.8 No.5
Finger vein images contain rich oriented features. Local line binary pattern (LLBP) is a good oriented feature representation method extended from local binary pattern (LBP), but it is limited in that it can only extract horizontal and vertical line patterns, so effective information in an image may not be exploited and fully utilized. In this paper, an orientation-selectable LLBP method, called generalized local line binary pattern (GLLBP), is proposed for finger vein recognition. GLLBP extends LLBP for line pattern extraction into any orientation. To effectually improve the matching accuracy, the soft power metric is employed to calculate the matching score. Furthermore, to fully utilize the oriented features in an image, the matching scores from the line patterns with the best discriminative ability are fused using the Hamacher rule to achieve the final matching score for the last recognition. Experimental results on our database, MMCBNU_6000, show that the proposed method performs much better than state-of-the-art algorithms that use the oriented features and local features, such as LBP, LLBP, Gabor filter, steerable filter and local direction code (LDC).
Yu, Lu,Chen, Yuan,Shi, Jie,Wang, Rufeng,Yang, Yingbo,Yang, Li,Zhao, Shujuan,Wang, Zhengtao The Korean Society of Ginseng 2019 Journal of Ginseng Research Vol.43 No.1
Background: Ginsenosides are known as the principal pharmacological active constituents in Panax medicinal plants such as Asian ginseng, American ginseng, and Notoginseng. Some ginsenosides, especially the 20(R) isomers, are found in trace amounts in natural sources and are difficult to chemically synthesize. The present study provides an approach to produce such trace ginsenosides applying biotransformation through Escherichia coli modified with relevant genes. Methods: Seven uridine diphosphate glycosyltransferase (UGT) genes originating from Panax notoginseng, Medicago sativa, and Bacillus subtilis were synthesized or cloned and constructed into pETM6, an ePathBrick vector, which were then introduced into E. coli BL21star (DE3) separately. 20(R)-Protopanaxadiol (PPD), 20(R)-protopanaxatriol (PPT), and 20(R)-type ginsenosides were used as substrates for biotransformation with recombinant E. coli modified with those UGT genes. Results: E. coli engineered with $GT95^{syn}$ selectively transfers a glucose moiety to the C20 hydroxyl of 20(R)-PPD and 20(R)-PPT to produce 20(R)-CK and 20(R)-F1, respectively. GTK1- and GTC1-modified E. coli glycosylated the C3-OH of 20(R)-PPD to form 20(R)-Rh2. Moreover, E. coli containing $p2GT95^{syn}K1$, a recreated two-step glycosylation pathway via the ePathBrich, implemented the successive glycosylation at C20-OH and C3-OH of 20(R)-PPD and yielded 20(R)-F2 in the biotransformation broth. Conclusion: This study demonstrates that rare 20(R)-ginsenosides can be produced through E. coli engineered with UTG genes.