分布式呼叫中心系统的设计

呼叫中心目前在各行各业中有着广泛的应用,但由于传统的集中式呼叫中心系统中存在语音服务平台和具体业务平台没有分离的缺点,对业务扩展产生了较大的阻碍。本文提出的分布式呼叫中心系统结构通过使用互联网络并采用分布式处理的思想对原有系统进行改造,将业务与呼叫中心通讯和设备控制分离,实现分布式的信息处理并简化业务流程控制,使系统整体的可扩展性和可维护性得到提升。     

Turbo／MAP编译码器中的交织器优化设计

讨论采用软输出迭代译交织级联卷积码（Ｔｕｒｂｏ码）编译码器中的交织器优化设计问题．从基于最大后验概率（ＭＡＰ）算法与迭代译码的Ｔｕｒｂｏ码编译码原理出发,给出交织器设计的一些基本方法并分析其特点;提出“保奇偶”的随机交织器设计方案,它能有效地改善某些以提高编码效率为目的的“删余截短”Ｔｕｒｂｏ码的纠错性能．通过计算机仿真得出一些Ｔｕｒｂｏ码在加性高斯白噪声信道中采用不同交织器时的误码率数据,分析了交织类型和交织深度的变化对Ｔｕｒｂｏ码纠错性能的影响．针对Ｔｕｒｂｏ码的特点提出了在卫星通信等应用中交织器设计的实用性结论．     

浅谈网络语言在词汇层面上的变异

随着网络在中国的迅猛发展,一种新的社会方言———网络语言兴起并蓬勃发展。互联网的出现对我们的生活产生了巨大影响。网络语言是广泛应用于虚拟世界的信息符号。网络语言与现实语言相比,它受现实语言的制约,同时又反作用于现实语言。本文试图从词汇层面对网络语言进行浅析。     

基于FLOWMASTER的制冷剂充注量对制冷系统性能影响的仿真研究

在分析制冷系统作用及基本原理的基础上,使用一维流体系统仿真软件FLOWMASTER的元件库建立了制冷系统仿真模型.用能量方程、动量方程和连续性方程联舍起来进行耦合求解,得到系统的温度和压力分布,进而得到流速及换热量等其它参数.在此基础上研究了制冷剂充注量对制冷系统性能的影响,得出了制冷量及COP（Coefficient of Performance,性能系数）随充注量变化的曲线,提出制冷剂的充注量要以制冷量达到设计要求时,系统的COP达到最大为原则.     

Granzyme B is recovered by natural killer cells via clathrin-dependent endocytosis

When they recognize a target cell, natural killer (NK) cells mount an attack to kill the target by exerting their cytotoxicity via the exocytosis of cytotoxic granules. Although the details of this process (which includes the movement of cytotoxic granules in the immune synapse and their fusion with the plasma membrane, releasing granzymes and perforin into the synaptic cleft) are relatively better understood, the post-exocytosis regulation of the process is still largely unknown. Here we show that a clathrin-dependent endocytosis stimulated by target cell occurs in NK92 cell line, which is closely correlated with granzyme B recovery. Inhibition of the endocytosis significantly attenuates the cytotoxicity of NK92 cells. The NK cell recovery of its released effector molecules, in turn, suggests that endocytosis may well play a key role in the post exocytosis regulation of immune cells.     

Maize HapMap2 identifies extant variation from a genome in flux

Whereas breeders have exploited diversity in maize for yield improvements, there has been limited progress in using beneficial alleles in undomesticated varieties. Characterizing standing variation in this complex genome has been challenging, with only a small fraction of it described to date. Using a population genetics scoring model, we identified 55 million SNPs in 103 lines across pre-domestication and domesticated Zea mays varieties, including a representative from the sister genus Tripsacum. We find that structural variations are pervasive in the Z. mays genome and are enriched at loci associated with important traits. By investigating the drivers of genome size variation, we find that the larger Tripsacum genome can be explained by transposable element abundance rather than an allopolyploid origin. In contrast, intraspecies genome size variation seems to be controlled by chromosomal knob content. There is tremendous overlap in key gene content in maize and Tripsacum, suggesting that adaptations from Tripsacum (for example, perennialism and frost and drought tolerance) can likely be integrated into maize.     

A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis

To identify susceptibility loci for ankylosing spondylitis, we performed a two-stage genome-wide association study in Han Chinese. In the discovery stage, we analyzed 1,356,350 autosomal SNPs in 1,837 individuals with ankylosing spondylitis and 4,231 controls; in the validation stage, we analyzed 30 suggestive SNPs in an additional 2,100 affected individuals and 3,496 controls. We identified two new susceptibility loci between EDIL3 and HAPLN1 at 5q14.3 (rs4552569; P = 8.77 × 10(-10)) and within ANO6 at 12q12 (rs17095830; P = 1.63 × 10(-8)). We also confirmed previously reported associations in Europeans within the major histocompatibility complex (MHC) region (top SNP, rs13202464; P < 5 × 10(-324)) and at 2p15 (rs10865331; P = 1.98 × 10(-8)). We show that rs13202464 within the MHC region mainly represents the risk effect of HLA-B*27 variants (including HLA-B*2704, HLA-B*2705 and HLA-B*2715) in Chinese. The two newly discovered loci implicate genes related to bone formation and cartilage development, suggesting their potential involvement in the etiology of ankylosing spondylitis.     

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

Leber congenital amaurosis (LCA) is a blinding retinal disease that presents within the first year after birth. Using exome sequencing, we identified mutations in the nicotinamide adenine dinucleotide (NAD) synthase gene NMNAT1 encoding nicotinamide mononucleotide adenylyltransferase 1 in eight families with LCA, including the family in which LCA was originally linked to the LCA9 locus. Notably, all individuals with NMNAT1 mutations also have macular colobomas, which are severe degenerative entities of the central retina (fovea) devoid of tissue and photoreceptors. Functional assays of the proteins encoded by the mutant alleles identified in our study showed that the mutations reduce the enzymatic activity of NMNAT1 in NAD biosynthesis and affect protein folding. Of note, recent characterization of the slow Wallerian degeneration (Wld(s)) mouse model, in which prolonged axonal survival after injury is observed, identified NMNAT1 as a neuroprotective protein when ectopically expressed. Our findings identify a new disease mechanism underlying LCA and provide the first link between endogenous NMNAT1 dysfunction and a human nervous system disorder.     

基于CBERS CCD数据的鹿洼煤矿塌陷区LUCC检测

本文基于多时相中巴地球资源卫星CBERS CCD数据,以鹿洼煤矿塌陷区为例,利用混合像元分解技术开展土地利用/覆盖变化LUCC检测.分别选取研究区域的2002年、2006年和2010年3个时相的CBERSCCD图像作为遥感数据源,将粒子群优化算法引入到端元提取中,基于线性光谱混合模型提取鹿洼煤矿塌陷区水体、建筑用地、农田和土壤4类地物信息,并对结果进行统计分析.LUCC检测结果表明,2002年至2010年间,鹿洼煤矿塌陷地面积逐年增加,造成大面积农田积水,导致无法进行作物耕种.最后,结合当地政府采取的塌陷地治理措施分析了土地利用变化情况.     

Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder

Transitional cell carcinoma (TCC) is the most common type of bladder cancer. Here we sequenced the exomes of nine individuals with TCC and screened all the somatically mutated genes in a prevalence set of 88 additional individuals with TCC with different tumor stages and grades. In our study, we discovered a variety of genes previously unknown to be mutated in TCC. Notably, we identified genetic aberrations of the chromatin remodeling genes (UTX, MLL-MLL3, CREBBP-EP300, NCOR1, ARID1A and CHD6) in 59% of our 97 subjects with TCC. Of these genes, we showed UTX to be altered substantially more frequently in tumors of low stages and grades, highlighting its potential role in the classification and diagnosis of bladder cancer. Our results provide an overview of the genetic basis of TCC and suggest that aberration of chromatin regulation might be a hallmark of bladder cancer.