We first design a discrete hyperchaotic system via piece-wise linear state feedback. The states of the closed loop system are locally expanding in two directions but absolutely bounded on the whole, which implies hype...We first design a discrete hyperchaotic system via piece-wise linear state feedback. The states of the closed loop system are locally expanding in two directions but absolutely bounded on the whole, which implies hyperchaos. Then, we use three suchlike hyperchaotic systems with different feedback gain matrices to design a pseudo-random sequence generator (PRSG). Through a threshold function, three sub-sequences generated from the output of piecewise linear functions are changed into 0-1 sequences. Then, followed by XOR operation, an unpredictable pseudo-random sequence (PRS) is ultimately obtained. The analysis and simulation results indicate that the PRS, generated with hyperchaotic systems, has desirable statistical features.展开更多
在面向卫星物联网的免授权随机接入(Grant-free Random Access,GFRA)系统中,受大规模连接和设备随机激活的影响,前导碰撞成为用户接入性能提升的主要制约因素。鉴于此,借助正交与非正交序列在前导检测和冲突抑制方面的各自优势,提出一...在面向卫星物联网的免授权随机接入(Grant-free Random Access,GFRA)系统中,受大规模连接和设备随机激活的影响,前导碰撞成为用户接入性能提升的主要制约因素。鉴于此,借助正交与非正交序列在前导检测和冲突抑制方面的各自优势,提出一种基于混合ZC(Zadoff-Chu)序列的大容量前导设计和检测方法。该方法利用正交ZC序列与其循环移位映射的不同根ZC序列级联来构建前导序列,并采用一种基于假设检验的两阶段干扰消除活跃用户检测算法,以确保大规模接入场景下的高精度用户识别。此外,对所提前导结构进行扩展,将相位旋转因子与多段非正交序列相结合,在不增加峰均比的前提下进一步扩大前导集容量。所提方法较现有复合和正交前导方法具有显著改善的多用户识别性能,在相同活跃用户下,成功检测概率最大提升约30.3%。展开更多
To screen genetic polymorphisms of Panax ginseng, as well as those of Panax quinquefolium and Panax notoginseng, analysis of random amplified polymorphic DNA （RAPD） was performed using 120 random primers. Of the suc...To screen genetic polymorphisms of Panax ginseng, as well as those of Panax quinquefolium and Panax notoginseng, analysis of random amplified polymorphic DNA （RAPD） was performed using 120 random primers. Of the successful amplicons obtained, the Panax ginseng-specific RAPD marker C-12 was cloned into a TA vector and sequenced （Genl3ank access number KU553472）. Based on the sequence analysis results, a pair of primers specific to C-12 was designed. Finally, a SCAR marker-based identification system for Panax ginseng was developed after optimization of the reaction conditions. Using this method, two positive bands were stably observed at 300 bp and 130 bp in 33 batches of Panax ginseng samples tested, while negative results were obtained for another 101 batches of samples, including Panax quinquefolium, Panax notoginseng, adulterants, and other medicinal herbs. Thus, we successfully developed a PCR-based method for rapid and effective identification of Panax ginseng, which can be effectively used for the protection and utilization of germplasm resources and identification of the origins of Panax ginseng samples.展开更多
基金This project was supported by the National Natural Science Foundation of China (69874025).
文摘We first design a discrete hyperchaotic system via piece-wise linear state feedback. The states of the closed loop system are locally expanding in two directions but absolutely bounded on the whole, which implies hyperchaos. Then, we use three suchlike hyperchaotic systems with different feedback gain matrices to design a pseudo-random sequence generator (PRSG). Through a threshold function, three sub-sequences generated from the output of piecewise linear functions are changed into 0-1 sequences. Then, followed by XOR operation, an unpredictable pseudo-random sequence (PRS) is ultimately obtained. The analysis and simulation results indicate that the PRS, generated with hyperchaotic systems, has desirable statistical features.
文摘在面向卫星物联网的免授权随机接入(Grant-free Random Access,GFRA)系统中,受大规模连接和设备随机激活的影响,前导碰撞成为用户接入性能提升的主要制约因素。鉴于此,借助正交与非正交序列在前导检测和冲突抑制方面的各自优势,提出一种基于混合ZC(Zadoff-Chu)序列的大容量前导设计和检测方法。该方法利用正交ZC序列与其循环移位映射的不同根ZC序列级联来构建前导序列,并采用一种基于假设检验的两阶段干扰消除活跃用户检测算法,以确保大规模接入场景下的高精度用户识别。此外,对所提前导结构进行扩展,将相位旋转因子与多段非正交序列相结合,在不增加峰均比的前提下进一步扩大前导集容量。所提方法较现有复合和正交前导方法具有显著改善的多用户识别性能,在相同活跃用户下,成功检测概率最大提升约30.3%。
基金Project(2014ZX09304307-002)supported by the Major Program of Science and Technology Foundation of ChinaProject supported by Technology Platform for Quality/Safety Inspection and Risk Management of Traditional Chinese Medicine,China+1 种基金Project(2014SK2001)supported by the Key Program Foundation of Hunan Provincial Science&Technology Department,ChinaProject(XSYK-R201502)supported by the Hunan Provincial Food and Drug Administration under Key Project of Science and Technology for Food and Drug Safety,China
文摘To screen genetic polymorphisms of Panax ginseng, as well as those of Panax quinquefolium and Panax notoginseng, analysis of random amplified polymorphic DNA （RAPD） was performed using 120 random primers. Of the successful amplicons obtained, the Panax ginseng-specific RAPD marker C-12 was cloned into a TA vector and sequenced （Genl3ank access number KU553472）. Based on the sequence analysis results, a pair of primers specific to C-12 was designed. Finally, a SCAR marker-based identification system for Panax ginseng was developed after optimization of the reaction conditions. Using this method, two positive bands were stably observed at 300 bp and 130 bp in 33 batches of Panax ginseng samples tested, while negative results were obtained for another 101 batches of samples, including Panax quinquefolium, Panax notoginseng, adulterants, and other medicinal herbs. Thus, we successfully developed a PCR-based method for rapid and effective identification of Panax ginseng, which can be effectively used for the protection and utilization of germplasm resources and identification of the origins of Panax ginseng samples.
