查询词典 sequence

Two gene fragments of DEN-1(GenBank accession number DQ886390)and DEN-2(GenBank accession number DQ886391),differentially expressed between the ocular skin tissues of normal and albino turbot,were isolated by mRNA differential display and sequenced.It was confirmed by RT-PCR method that the expression levels of both DEN-1 and DEN-2 were down-regulated in the ocular skin tissue of albino turbot.The sequence homology search of DEN-1 revealed high sequence homologies with the UGGT genes of zebrafish and cattle,and the Ugcgl1 gene of Norway rat.High sequence homologies of DEN-2 were observed with the eya4 gene(the eye absent homolog 4)from red jungle fowl,zebrafish,human,Norway rat,mouse and dog.

应用mRNA差异显示技术，对比研究正常与白化大菱鲆有眼侧皮肤组织，克隆差异表达基因，经测序，RT-PCR 验证，差异表达基因片段DEN-1(GenBank登录号：DQ886390)与DEN-2(GenBank登录号：DQ886391)均在白化大菱鲆有眼侧皮肤组织中下调表达；通过BLAST检索发现，DEN-1与GenBank中的斑马鱼和牛的类似尿苷二磷酸-葡萄糖：糖蛋白葡糖基转移酶基因、与挪威鼠类似尿苷二磷酸-葡萄糖：神经酰氨葡糖基转移酶1(Ugcgl1)基因有较高同源性；DEN-2 与原鸡、斑马鱼、人、挪威鼠、家鼠和狗的眼缺乏同源框4(eya4)基因的同源性均较高。

If one sequence is shorter than the other and all its elements match the corresponding elements in the longer sequence, then the shorter sequence is lexicographically smaller.

如果一个序列比另一个短，并且它的元素与较长序列中对应元素相匹配，则较短的序列在字典序上较小。

In the method of the invention, a baseband signal is pre-processed to realize nonlinearity compensation. The pre-processing method comprises the following steps: the filter coefficient and the multinomial coefficient of the high power amplifier are extracted; corresponding gain is calculated for the amplitude value of each point input into the sequence of the baseband signal, and the phase compensation value is calculated according to the amplitude gain; the phase compensation value and the gain which are corresponding to each point are synthesized into re-gain, a pre-processing value pi is obtained, and pre-processing output sequence is formed; the pre-processing output sequence is output into the high power amplifier directly or through a inverse filter.

本发明方法是将基带信号进行预处理来实现抵偿非线性，预处理方法是：提取出高功率放大器的滤波器系数和多项式系数；对输入基带信号序列中的每一点的幅值计算对应的增益，根据幅度增益计算出相位补偿值；每一个点对应的相位补偿值与增益合成复增益，得到预处理值p i ，构成了预处理输出序列；将预处理输出序列直接或经过反向滤波器后输出到高功率放大器中。

Pairwise sequence alignment is one of common methods in analyzing sequence, which also is the base of multiple sequence alignment and data search.

双序列比对是序列分析常用的方法之一，也是多序列比对和数据库搜索的基础。

In order to compare the homology of the gene encoding VP2 between MDPV-Q and MDPV which was registered in the GenBank, also in order to find out changes of the VP2 gene and the immuno-genicity between the wild-strain MDPV-Q and the attenuated strain MDPV-26 which derived by continued passage of virulent wild-type in muscovy duck embryo, a pair of primer (LHMP7/LHMP8) was designed. The upper one LHMP7 and the lower one LHMP8 corresponded to the MDPV-specific nucleotides sequence 2885-2900 and 4618-4604 respectively, according to the MDPV nucleotide sequence databases. The length of the sequence embraced by the primers was 1734bp.

为了获取这一基因片段与国外分离株进行同源性比较，同时也为了了解MDPV强、弱毒株VP2基因之间的异同关系，及其免疫原性的变化规律，通过DNA重组技术，设计了一对引物LHMP7／LHMP8，该对引物选取位于2885～2900及4618～4604的两段序列，跨幅为1734bp，并在这两条引物中分别加入两种限制性核酸内切酶SacⅡ和KpnⅠ的酶切位点，分别对MDPV-Q和由该株病毒经人工致弱后得到的MDPV-26株进行PCR扩增，并将PCR产物克隆到pMD18-T载体上，分别得到二个重组子：pMD18-T—M-Q VP2和pMD18-T-M-26 VP2。

The amplified band from M131 was sequenced and then aligned with the sequence of avr-Pila gene. The result was that the sequence was 98% homologous to one fragment of avr-Pita sequence, but the integration site was not within this fragment.

将M131的扩增片段测序后得到长度为1057bp的序列，并且将所测序列和已知的avr-Pita一段序列比较发现达98％的同源，即该序列为无毒基因的某一段序列，但插入的位点并不在所扩增片段内。

The amplifiedband from M131 was sequenced and then aligned with the sequence of avr-Pila gene. The result was that the sequence was 98% homologous to one fragment of avr-Pita sequence, but the integration site was not within this fragment.

将M131的扩增片段测序后得到长度为1057bp的序列，并且将所测序列和已知的avr-Pita一段序列比较发现达98％的同源，即该序列为无毒基因的某一段序列，但插入的位点并不在所扩增片段内。

The PCR product was cloned into PGEM-T-Easy DNA plasmid by TA cloning, and hINS gene was analyst and compared to the published sequence ,and found that this hINS gene is same to one of the published sequence and there are four different bases with the other published sequence.

为了进一步验证扩增出的hINS基因能否在蛋白质水平上表达，用构建的乳腺特异性表达载体制作转基因小鼠，利用转基因小鼠作为个体表达系统来检测目标蛋白表达量。

By NCBI BLASTX server, tomato P56 amino-acid sequence was compared with other pectate and pectin lyases belonging to polysaccharide lyase family Ⅰ 28 proteins ,with higher identity of amino acid sequence compared to P56 amino-acid sequence, were obtained.

利用NCBI BLASTX服务器，搜索与番茄P56蛋白氨基酸序列相似且都属于多糖裂解酶家族Ⅰ的果胶裂解酶蛋白序列共28条，用DNAMAN软件分析其保守区，用CLUSTALX8.0软件进行序列比对和Bi-oEdit软件进行文件转换，进一步用PUAP4.0软件构建系统进化树。

The species observed can be categorized into 5 kinds of Fibonacci sequence groups based on the sequence of phyllotaxy and golden divergence angle. At the same time, by comparing the existing documentation, we explore the difference and relation among different taxa, in addition, the difference between environments in order to explicate the factors influencing the sequence of phyllotaxy.

藉由叶序之序列及黄金分离角，可将观察之物种，分为5种费氏序列类群，同时比对既有的文献纪录，探讨不同分类群间的差异，以及分类群间的关系，并分析环境之间的差异，藉此说明影响叶序配列的因子。

As of Tuesday, Google's results were still censored in China.

截至周二，谷歌的搜索结果仍受中国审查。

In order to make the positive action increase and negative one decrease, the sub-forces of the social factors must be adjusted to form a centripetal force.

在这一过程中，人的主体性发挥是社会有机体健康发展的灵魂。