编码信号

Blend various advantages of the coding project of the parameter audio frequencies in the meantime, carried on adjustment on the coder structure, have to a certain signal more the mold piece of coding result, if wave structure analytical transformation short time of the mold piece, double the composition examine and double the transformation short time mold piece etc. is an options to bring into coder, from user while coding according to small together source voice document of small together characteristics, decide whether use and how use, but these vivid constitutions can through a code flow in define several good to mark ratio in advance tell a decoding machine especially, constituting decoding machine is little with complications to without direct influence.

同时融合多种参数音频编码方案的优点，在编码器结构上进行了调整，将只对某类信号有较好编码效果的模块，如谐波结构分析模块、双变换短时成分检测与双变换短时模块等，作为选项纳入到编码器中，由使用者在编码时根据小同源声文件的小同特点，来决定是否使用和如何使用，而这些灵活的设置都可以通过码流中预先定义好的几个标示比特位来告知解码器，对解码器本身的构成与复杂度少没有直接的影响。

Dual Encoder to USB Converter module can handle signals from 2 SSI absolute encoders or 2 quadrature incremental encoders.

双编码USB转换模块可以处理的信号2小型工业绝对式编码器或2正交增量编码器。

The result showed that twocDNA fragments which expressed at high level both in shoot and radicle representedthe gene encoding beta-D-glucosidase; one cDNA fragment expressed specifically inshoot represented the gene encoding mitochondria HSP60; most clones of MF12 andMF17 fragments respectively represented the chloroplast genes encoding prp22 andprp19 proteins which are two components of ribosomal small subunit; while thededuced amino acid sequence from each exceptional one clone was respectivelyhomologous to CDC5 proteins and vesicle-associated membrane proteins; otherthree cDNA fragments expressed preferentially in shoot had no homologue inGenBank.

结果发现2个在胚芽和胚根中表达量都很高的cDNA片段代表的是编码玉米β-D-葡糖苷酶的基因；一个在胚芽中表达而在胚根中不表达的片段代表的是编码线粒体分子伴侣HSP60的基因；片段MFl2的大部分克隆测序结果是与叶绿体基因组中编码核糖体小亚基蛋白prp22的基因同源，但其中有一个克隆测定的cDNA片段序列推测的氨基酸序列与CDC5家族成员有较高的同源性；片段MF17的大部分克隆测序结果与叶绿体基因组中编码核糖体蛋白prp19的基因同源，而有一克隆测定的cDNA片段序列推测的氨基酸序列与参与信号转导的膜结合蛋白VAP27和VAMP有较高的同源性；另有3个优先在胚芽中表达的cDNA片段未查询到同源序列。

This thesis discussed three kinds of major technologies to reduce high PAR on the basis of the principle of OFDM system: pre-distortion technology techniques (clipping and filtering, peak windowing and companding technique), code techniques (Reed-Muller coding algorithm of Golay complementary sequence), and scrambling techniques (selected mapping, partial transmit sequence and selective scrambling), these techniques have some certain limitations.

本文在介绍OFDM理论的基础上，专题讨论了抑制高峰值平均功率比的三类主流技术：信号预畸变技术(限幅滤波、窗函数和压扩技术)、信号编码技术(Golay互补序列的Reed-Muller编译码算法)和信号扰码技术(选择性映射技术、部分传输序列技术和选择性扰码)。

The present invention relates to a method for heuristically starting up DC brushless servo electric machine, including the following steps of (1) after powerup of an increment type photoelectric encoder, electrifying a stator winding two by two with identical time interval to generate six-directional stator winding resultant magnetic fields;(2) detecting six different angles rotated by the rotor within identical tiny time interval by the photoelectric encoder;(3) selecting most positive value rotation angle from the six different angles, and determining maximum torque corresponding to the stator winding resultant magnetic field, and implementing servo startup using the maximum torque as constant starting torque;(4) after the zero-point signal of the photoelectric encoder occurring, switching to servo operation with normal constant torsion.

本发明直流无刷伺服电机试探启动方法，采用如下步骤：(1)增量式光电编码器上电后对定子绕组采用相同的时间间隔两两通电，顺序产生六个方向的定子绕组合成磁场；(2)由增量式光电编码器检测出转子在相同的微小时间间隔内分别转过的六个不同的角度；(3)从转子六个不同的角度中选出最大正值的转角，确定相应定子绕组合成磁场对应的最大转矩，并以该最大转矩为恒定启动转矩进行伺服启动；(4)当增量式光电编码器零点信号出现后，切换为正常恒转矩伺服运行。

The deduced amino-acid sequence of the TcGH had 210aa,including a putative signal peptide (22aa) located at its N-terminal. The homology of the TcGH amino-acid with relative species grass carp,black carp,bighead carp,carp,zebra fish,etc.

结果序列分析表明：唐鱼GH cDNA的5 非编码区为64 bp，3 非编码区为448 bp，开放阅读框633 bp，共编码210个氨基酸，包括22个氨基酸的信号肽和188个氨基酸的成熟肽。

Signal peptide sequence was removed lest it couldnt be recognized by Bacillus subtilis, gene coding for mature peptide was ligated to downstream of sacB signal peptide sequence of pWB980 to form a new ORF and generate pWB980-LipA, gene coding for its chaperone was also amplified and ligated to the downstream of LipA to generate a secretion/expression vector pWB980-LipAB.thechaperone gene was sequenced and analyzed by multiple alignments, resulted showed that there were mutations of nucleotides(1～7) and amino acids (1～2) with the other reported genes.

为了防止枯草芽孢杆菌信号肽酶不能识别脂肪酶的信号肽，切除掉脂肪酶的信号肽编码序列，与枯草芽孢杆菌分泌表达质粒pWB980连接并与质粒上的SacB信号肽构成一个完整的开放式阅读框，获得重组质粒pWB980-LipA，因为该脂肪酶的活性表达需要一个特异性分子伴侣帮助折叠成有活性的构象，将脂肪酶分子伴侣基因串连到脂肪酶基因的下游，获得重组分泌表达载体pWB980-LipAB并且测序分析分子伴侣的基因序列和氨基酸序列并与其它报导的序列进行了比对，发现有1到7个碱基的差异和1到2个氨基酸残基的突变。

The development of electrical fast interpolation device and the function of the photoelectrical rotary encoder is introdu...

本论文介绍了莫尔条纹细分技术的发展及其在光电轴角编码器中的作用，详细说明了高分辨率光电轴角编码器的组成及工作原理，对光电轴角编码器莫尔条纹信号高插补系数快速电子学细分装置进行了硬件、软件设计，并进行了精度分析。

Server agent coded by writer is presented in detail through the SART method,and some creative key technologies are analyzed such as the combination of the software signal、the properties of process and process communication that not only solved the real monitoring problem;the adoption of the UNIX phoney system-PROCFS that not only solved the real monitoring problem;Encoding and decoding to SNMP message on BER-solved the problem on monitor between several operating system.

文章最后给出了笔者负责编写的服务器代理的实现技术，采用SART方法对服务器代理的整体框架和各组成模块进行了详细描述，并对编码过程中的一些创新技术进行了分析，如：将UNIX系统中软件中断信号、UNIX进程的特性和进程间通信有机的结合起来，解决了代理的启动/关闭进程、探测进程状态等实际监控难题；利用UNIX系统的伪文件系统PROCFS进行资源探测，解决了系统中不能用SNMP进行探测的实际监控难题；采用BER编码规范对SNMP报文编码和解码，解决了系统中利用SNMP进行跨平台监控的难题。

We found that neither the fusioned nor the non-fusioned forms of Hu-P68 cDNA open reading frame could express efficiently in the E. coli cells; in different prokaryotic expression vectors and under various promotors resulted in no distinctive variations. Deletion of 5'UTR by synthesis adaptors, deletion of 3'UTR or signal peptide sequence by PCR gained no gross improvement. Only the truncated API-I proteins were observed to be highly expressed when the 3'ORF fragment of the Hu-P68 cDNA was fusioned at the 3'end of PAI-I gene.

结果发现无论是以融合形式存在，还是以非融合形式存在，人的P68 cDNA基因在E.coli细胞中都未能获得高效表达：在不同表达载体中，不同启动子对P68 cDNA基因的表达没有显著差异；利用合成Adapter的方法删除5'UTR，及利用PCR技术删除3'UTR和信号肽序列对表达没有明显改善；分别表达被分割的P68 cDNA5'端编码区、中央编码区和3'端编码区均未见有明显表达；当P68 3'端编码区与高效表达蛋白PAI-Ⅰ基因3'末端融合时，仅见有PAI-Ⅰ以截断形式高效表达出来。

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。