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31.
针对音频信号准确性分类的问题,提出一种基于改进的的粒子群优化算法(PSO)的支持向量机(SVM)音频信号分类的方法,简称IPSO-SVM.首先用Mel倒谱系数法对4种音频信号进行特征提取.其次在PSO中引入自适应变异因子,能够成功地跳出局部极小值点;然后对PSO中的惯性权重进行了改进,将惯性权重由常数变为指数型递减函数.随着迭代的进行,使权重逐渐减小,这样做有利于粒子进行局部寻优.最后用改进的PSO不断优化SVM中的惩罚因子c和核函数参数g来提高预测精度.实验结果表明,与传统的SVM、PSO-SVM、GA-SVM相比,我们提出的IPSO-SVM算法分类结果更精确. 相似文献
32.
33.
以双向环形耦合Duffing振子系统为对象, 研究脉冲信号激励下耦合振子间动力学行为变化特征时, 发现其与单向环形耦合Duffing振子系统类似, 在一定的参数条件下, 脉冲信号能引起其中一个振子与其他振子运动轨迹间出现短暂失同步的现象即瞬态同步突变现象. 基于这种现象, 提出了一种微弱脉冲信号检测的新方法, 用于检测强噪声背景中的局部放电脉冲信号. 实验测试表明, 利用本文方法对不同放电电极的局部放电脉冲信号进行检测时, 在低信噪比条件下可取得良好的检测效果, 进而扩展了现有的Duffing振子对非周期信号的检测范围及应用领域.
关键词:
耦合Duffing 振子
微弱信号检测
瞬态同步突变
局部放电脉冲信号 相似文献
34.
Through studying several kinds of chaotic mappings‘ distributions of orbital points, we analyze the capabilityof the chaotic mutations based on these mappings. Nunerical experiments support our conclusions very well. Thecapability analysis also led to a self-adaptive mechanism of chaotic mutation. The introducing of the self-adaptivechaotic mutation can improve the performance of genetic algorithm very prominently. 相似文献
35.
Triplet state sublevel spectroscopy using optical detection of magnetic resonance (ODMR) in zero magnetic field can be successfully
employed to study (i) the environment of tryptophan (Trp) residues in a protein by observing the position and structure of
phosphorescence spectra, zero field ODMR transitions and triplet state sublevel kinetics, (ii) the energy transfer among Trp
residues, and (iii) whether any cysteine (Cys) residue is within van der Waals distance of any Trp residue by studying the
complex of the protein with methylmercury(II) iodide (CH3HgI) which binds to Cys residues. These studies are particularly important where crystal structure study is not possible.
Study of the S1 state often gives ambiguous results since fluorescence is always broad and shows multi-exponential decay. Our results on
bacteriophage lysozyme T4 which contains three Trp residues at positions 126, 138 and 158 are presented. Measurements were
facilitated by the use of a mutated enzyme containing one or two Trp-Tyr substitutions. The results indicate that (i) Trp
126 and 158 are solvent exposed, whereas Trp 138 is buried in a hydrophobic environment, (ii)S ↔S non-radiative energy transfer takes place predominantly from Trp 126 to Trp 158, and (iii) only Trp-158 undergoes a heavy
atom perturbation, which affects selectively the z-sublevel (z is an out-of-plane axis of the indole plane) as a result of
CH3HgI binding to nearby Cys 97. We suggest that the Hg atom is located on the z-axis of Trp 158 in the complex. This interpretation
is based on our investigations on the effect of orientation of heavy atom perturbers in some naphthalene-crown ether metal
ion complexes. 相似文献
36.
Marquette CA Degiuli A Imbert-Laurenceau E Mallet F Chaix C Mandrand B Blum LJ 《Analytical and bioanalytical chemistry》2005,381(5):1019-1024
Two diagnostic chemiluminescent biochips were developed for either the detection of p53 gene point mutation or the serological detection of anti-HIV-1 p24 capsid protein. Both biochips were composed of 24 microarrays of latex beads spots (4×4) (150 m in diameter, 800 m spacing) entrapped in a poly(dimethylsiloxane) elastomer (PDMS). The latex beads, bearing oligonucleotide sequences or capsid protein, were spotted with a conventional piezoelectric spotter and subsequently transferred at the PDMS interface. The electron microscopy observation of the biochips showed how homogeneous and well distributed the spots could be. Point mutation detection on the codon 273 of the p53 gene was performed on the basis of the melting temperature difference between the perfect match sequence and the one base pair mismatch sequence. The hybridisation of a 20-mer oligonucleotide form the codon 273 including a one base pair mutation in its sequence on a biochip arrayed with non-muted and the muted complementary sequences, enabled a clear discrimination at 56°C between muted and wild sequences. Moreover, the quantitative measurement of the amount of muted sequence in a sample was possible in the range 0.4–4 pmol. Serological measurement of anti-HIV-1 p24 capsid protein on the biochip, prepared with 1-m-diameter latex beads, enabled the detection of monoclonal antibodies in the range 1.55–775 ng mL–1. Such a range could be lowered to 0.775 ng mL–1 when using 50-nm-diameter beads, which generated a higher specific surface. The validation of the biochip for the detection of anti-HIV-1 capsid protein antibodies was performed in human sera from seropositive and seronegative patients. The positivity of the sera was easily discriminated at serum dilutions below 1:1,000. 相似文献
37.
Richard Varro 《代数通讯》2013,41(7):2426-2448
We give the identities generating the spaces of degree 4 multilinear identities satisfied by the non commutative 0th-order Bernstein algebras and the non commutative mutation algebras. For it, we use a method reducing the search for multilinear identities to the resolution of linear systems. 相似文献
38.
Vanessa Labet André Grand Prof. Jean Cadet Prof. Leif A. Eriksson Prof. 《Chemphyschem》2008,9(8):1195-1203
Five pathways leading to the deamination of cytosine (to uracil) after formation of its deprotonated radical cation are investigated in the gas phase, at the UB3LYP/6‐311G(d,p) level of theory, and in bulk aqueous solvent. The most favorable pathway involves hydrogen‐atom transfer from a water molecule to the N3 nitrogen of the deprotonated radical cation, followed by addition of the resulting hydroxyl radical to the C4 carbon of the cytosine derivative. Following protonation of the amino group (N4), the C4? N4 bond is broken with elimination of the NH3?+ radical and formation of a protonated uracil. The rate‐determining step of this mechanism is hydrogen‐atom transfer from a water molecule to the cytosine derivative. The associated free energy barrier is 70.2 kJ mol?1. 相似文献
39.
Choi BO Hwang JH Kim J Cho EM Cho SY Hwang SJ Lee HW Kim SJ Chung KW 《Experimental & molecular medicine》2008,40(3):354-360
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a genetically heterogeneous mitochondrial disorder with variable clinical symptoms. Here, from the sequencing of the entire mitochondrial genome, we report a Korean MELAS family harboring two homoplasmic missense mutations, which were reported 9957T>C (Phe251Leu) transition mutation in the cytochrome c oxidase subunit 3 (COX3) gene and a novel 13849A>C (Asn505His) transversion mutation in the NADH dehydrogenase subunit 5 (ND5) gene. Neither of these mutations was found in 205 normal controls. Both mutations were identified from the proband and his mother, but not his father. The patients showed cataract symptom in addition to MELAS phenotype. We believe that the 9957T>C mutation is pathogenic, however, the 13849A>C mutation is of unclear significance. It is likely that the 13849A>C mutation might function as the secondary mutation which increase the expressivity of overlapping phenotypes of MELAS and cataract. This study also demonstrates the importance of full sequencing of mtDNA for the molecular genetic understanding of mitochondrial disorders. 相似文献
40.
We study quivers with relations given by noncommutative analogs of Jacobian ideals in the complete path algebra. This framework
allows us to give a representation-theoretic interpretation of quiver mutations at arbitrary vertices. This gives a far-reaching
generalization of Bernstein–Gelfand–Ponomarev reflection functors. The motivations for this work come from several sources:
superpotentials in physics, Calabi–Yau algebras, cluster algebras.
相似文献