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timing sequence相关的网络例句

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The main contributions of this paper include,(1) introduces the backtracking mechanism into traditional GEP methods and proposing a new algorithm named GEP with backtracking strategy.(2) Proposes the concept of Backtracking Checkpoint and designing Geometric Proportion Increased Checkpoint Sequence and Accelerated Increased Checkpoint Sequence to restrict the backtracking process.(3) Extends the GEPBS algorithm by introducing a Retrogression Factor to control the percentage of backtracking.(4) Proves the effectiveness of the new algorithm by two extensive experiments, which show that new method increases the max fitness by 49.2

本文的主要工作包括:(1)在传统GEP算法中引入回溯机制,提出基于回溯策略的GEP算法(GEP with backtracking strategy ,GEPBS);(2)提出回溯检查点概念,设计了等比递增检查点序列和加速递增检查点序列用于约束回溯过程;(3)扩充基于回溯的GEP算法,设计了退化因子,提出了按比例回溯策略(GEP with proportional backtracking strategy, GEPPBS)(4)通过两个实验验证了新算法的有效性,在相同条件下较传统算法的适应度最大提高了49.2%,成功率最高提高了4倍

By analyzing the N-terminal amino acid sequence and searching in NCBI database, we found SBP117 is a member of proline-rich protein family and its function is unknown. The registered number is AAO72557.1. The composition of amino acids of this protein is similar with those proteins found in diatom and cucumber, but the sequence of amino acids is different. It means that SBPl 17 is a special protein for graminaceous plants to control the silica deposition.

通过N-末端测序和查询NCBI数据库,鉴定了SBP117是一种未知功能的富脯氨酸蛋白家族的成员,其蛋白质序列号为AAO72557.1,它的氨基酸组成与硅藻和黄瓜中发现的硅结合蛋白相似,但排列顺序明显不同,说明其可能是一种禾本科植物所特有的控制硅沉积代谢的蛋白。

The protein encoded by this sequence was deduced to be consisted with 213 amino acids, signal peptide sequence from 1 to 17 position, and transmembrane regions from 171 to 190 position, whose grand average of hydropathicity is computed to be 0.031, secondary structure is composed by alpha helix (57.28%), extended strand (6.57%) and random coil (36.15%), subcellular localization was cytoplasmic by CELLO v.2.5. There are some function sites predicted by PROSCAN software, such as one N-glycosylation site (151-154aa), one protein kinase C phosphorylation site (193-195aa), two casein kinase II phosphorylation sites (155-158aa and 173-176aa), and one N-myristoylation site (97-102aa).

推测编码蛋白由213个氨基酸组成,信号肽序列位于1-17aa,亲水性指数为0.031,跨膜区域位于171-190aa,二级结构由-螺旋(57.28%)、延伸主链(6.57%)和无规卷曲(36.15%)组成;亚细胞定位于细胞质,含有N-糖基化位点1个(151-154aa),蛋白激酶C磷酸化位点1个(193-195aa),酪蛋白激酶Ⅱ磷酸化位点2个(155-158aa and 173-176aa),N端酰基化位点1个(97-102aa)。

The PCR production sequence length of them were 539bp and 498bp respectively, the same region sequence of mule chicken were the same as Guinea fowl or black normal feather Wugu chickens.

黑羽常羽乌骨鸡和珍珠鸡的线粒体D环高变区序列存在长度变异,乌骨鸡的此段序列长度为539hp,珍珠鸡的序列是498hp,而骡鸡个体的此段序列或同于乌骨鸡、或同于珍珠鸡。

Based on those analyses, a novel training sequence design method is proposed and the Hadamard matrix is used. Computer simulations are conducted to evaluate the optimum training sequence construction methods for TU and HT delay profiles.

在此基础上提出了一种利用Hadamard矩阵构造训练序列的新方法,并在TU和HT两种衰落信道条件下进行了仿真。

Based on the theory of instantaneous reactive power, the multiple frequency rotate transform theory is put forward. It overcomes the defect of that the theory of instantaneous reactive power can only measure the harmonic total amount. The positive sequence and negative sequence k-multiple frequency rotate coordinate is respectively put forward in detail.

倍频旋转变换理论是基于瞬时无功功率理论提出的,它克服了瞬时无功功率理论测量方法只能测量谐波总量的缺陷,该理论分别针对正序谐波和负序谐波,提出正向和负向倍频旋转坐标,通过k—倍频旋转坐标可将k次谐波分离出来。

For example, we have conducted the sequence screening on the binding sites of the interface of Barnase/Barstar complex and found that our DGA method can not only determine which position is more conservative and more important, but also redesign the binding sites rationally. The random sequence design for α,β,α/β and α+β four folding motifs have also been practiced and revealed that there are both homology evolution and heterology evolution of protein sequences compatible the same backbone motif.

例如,通过对典型的Barnase/Barstar复合物界面研究发现,它可以确定界面结合位点的重要性和保守性,并对结合位点进行合理的序列重新设计;通过对α、β、α/β、α+β等四种折叠模式骨架的随机序列设计,发现在蛋白质进化过程中,对同一种结构模式同时存在序列的同源进化和非同源进化这两种趋势。

Sequence analysis showed a high similarity in ITS sequence among these Hevea species, which varied only in several bases.

序列分析结果表明橡胶树属植物的ITS序列具有高度的相似性,仅存在几个碱基差别。

On the basis of an EST sequence of Hevea MYC-like gene in Genbank, we obtained the complete sequence of this gene using the methods of PCR and RACE.

该基因序列的长度为1817bp,包含一个1428bp的阅读框,编码476个氨基酸。推导的HbMYC1分子量为53.78 kD,等电点为6.20。

At the same time this paper constructs the probabilistic model of output sequences of the editing generator, and takes careful analysis on its structure, then examines the homogeneous markovian property of output sequences' indexes expressed as the form of basal sequence, proves that the output sequence of the editing generator is homogeneous Markov chain, and then synthetically analyzes and studies the cryptography property of the editing generator.

同时本文通过分析"编辑生成器"产生序列的过程,建立了"编辑生成器"的概率模型,考查了以基础序列表示的输出序列下标的齐次马氏性,证明了"编辑生成器"输出序列是齐次马氏链,并给出了其一步转移概率矩阵与k步转移概率矩阵,然后对概率模型的输出序列的性质进行了综合的分析和研究。

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