序列性

The pitch organization logic of pentatonic twelve-tone is the most important structure logic in Luo Zhongrong's twelve-tone music works, mainly composed of two structure types: pentatonic tonality serial and pentatonic atonality serial.

五声性十二音的音高组织逻辑是罗忠镕十二音作品中最重要的结构逻辑，主要有五声性调性序列和五声性非调性序列两种结构类型。

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。

At home and abroad published the same 24 NDV sequence homology analysis showed that the nucleotide sequence homology of 80%-98.4%, and amino acid homology of 87.2%-98.2% in between.

与国内外发表的24株 NDV 相同序列的同源性分析表明，其核苷酸序列的同源性在80％－98.4％之间，氨基酸同源性在87.2％－98.2％之间。

The total RNA was abstracted from the larvae of Boophilus microplus, and a 1982bp Bm86 gene was amplified by RT-PCR. The target gene was subcloned into T vector. The sequencing showed that the nucleotide sequence of the cloned Bm86 gene shared 97.4% homology with the data published in and this fragment contained the complete open reading frame of Bm86 gene.

为了克隆微小牛蜱Bm86 基因及构建该基因的表达载体，以微小牛蜱饥饿幼蜱的破解物提取的总RNA为模板，参照已发表的微小牛蜱Bm86基因的核苷酸序列，设计了1对引物，采用RT-PCR技术获得微小牛蜱Bm86基因；将Bm86基因克隆入载体，并进行序列分析，结果证明，克隆的Bm86基因序列与GenBank上登录的Bm86基因序列的同源性达97.4%，而且该序列包含完整的开放阅读框。

The basic principle and hierarchical frame of FSR decision-making solving for DN is proposed creatively based on reliable knowledge. The categoricalness and high efficiency of decision-making solution set for FSR are ensured. The principle layer controls and realizes the search range and realization mode. The hierarchy and subarea search is performed, whose optimal rule is considered at the same time in order to ensure the solving rapidity. The decision-making realization layer forms the operation sequence of switch based on the trunk network set algorithm. The categoricalness and high efficiency of decision-making solution set for FSR is ensured.

创造性的提出了基于可靠性知识的配电网故障恢复决策解集构造的基本原理和实现的层次结构：确保恢复处理决策解集构造的完备性与高效性；原则层控制实现解集的搜索范围及实现模式，按兼顾优化原则的分层、分区搜索并确保求解的快速性；决策实现层在实现模式和相应树干网集运算的基础上，形成恢复处理决策开关操作序列，确保决策开关操作序列形成的高效率。

The fragement of 261 bp was 86 percent the same as a part of the original sequence of Vulgare HortI gene, and the 105 bp was 96 percent compared with a part of the triticum monococcum phosphatidylserine decarboxylase gene. Both of them included an open reading frame.

测序比较261 bp片段与大麦属Vulgare HotrI基因部分序列同源性达86%，105bp片段与一粒小麦磷脂酰丝氨酸脱羧酶基因部分序列同源性高达96%。2个测序片段均包含开放阅读框序列。

Results The homologies of nucleotide sequences of amplified flhA, flhB2 and fliR genes to those reported were 100%, 99.9% and 99.9%, and those of the deduced amino acid sequences were 100%, 100% and 99.8%, respectively.

结果 问号钩体56601株flhA、flhB2和fliR基因扩增片段的核苷酸序列与报道的相应序列同源性分别为100%、99.9%和99.9%，氨基酸序列同源性分别为100%、99.8%和100%。

The three isolates were named A/Bar-headedGoose/Qinghai/F/2006(H5N1), A/Black-headed Gull/Qinghai/3/2006(H5N1) andWhooper Swan/Qinghai/01/2006(H5N1). The research results were, nucleotidesequence analysis revealed that three isolates shared a high homology with each other(99%) except PB1 genes of Bar-headed Goose/Qinghai/F/200 and Whooperswan/Qinghai/01/2006, which shared 94% identity.

通过对3株病毒的全基因组序列分析与进化研究，其分子特征分析结果显示：Whooper swan／Qinghai／01／2006株和Bar-headed Goose／Qinghai／F／2006株的PB1基因的核苷酸序列同源性为94％之外，3株病毒其余基因片段的核苷酸序列同源性为99％。

Results Five of the PCR amplifications were discovered and sequenced with 300 bp ...

结果对 5个阳性标本的 30 0bp部分M基因组片段序列分析表明均为SEO型汉坦病毒；毒株核苷酸序列比较表明：与其他SEO型毒株同源性均达 94%以上，而与其他HNT型毒株同源性均低于 72 %；毒株序列所构建的系统发生树显示，北京地区SEO型汉坦病毒可能至少存在 4个不同的进化分支和两个不同的汉坦病毒亚型。

The phylogenetic tree was constructed using maximum evolution approach in Mega. The negative selection sites were analyzed by using Datamonkey. There is an apparent 30 bp nucleotides deletion mutation in homonids FKN comparing to that of Old World Monkeys besides other point mutations. Homology of nucleotide sequence between human and chimpanzee, gorilla, orangutan, gibbon, macaque and leaf monkey is 99.2%、98.4%、98.1%、96.5%、95.9% and 93.8% respectively. Homology of amino acid sequence of them is 98.5%、98.0%、97.7%、94.7%、93.7% and 90.5% respectively.

序列分析发现人猿超科较旧大陆猴FKN基因除了有散在的点突变外，还有一明显的30bp的核苷酸缺失突变；人FKN基因序列与黑猩猩、大猩猩、红毛猩猩、长臂猿、猕猴和叶猴的同源性分别是99.2%、98.4%、98.1%、96.5%、95.9%和93.8%，由此推导的氨基酸序列同源性分别是98.5%、98.0%、97.7%、94.7%、93.7%和90.5%；FKN基因进化树表明人与黑猩猩关系更近，FKN基因进化和通常认为的物种进化一致；Datamonkey分析结果显示FKN存在3个负选择位点53Q、84D、239N。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。