FGS比特流的差错复原性能

基于IP的视频通信不可避免地要面临信道差错的影响，如比特误码和分组丢失。可分级编码是解决这些问题的重要方法之一。FGS(Fine Granularity Scalabmty)是一种全新的可分级编码方法，它能提供非常精细的可分级编码能力。研究了FGS比特流在IP网络上的传输特性，并为FGS比特流引入了一种差错还原打包方案。仿真结果表明，该打包方案可以明显地改善FGS比特流的差错还原能力。     

Sorting nexin 3 mutation impairs development and neuronal function in <Emphasis Type="Italic">Caenorhabditis elegans</Emphasis>

The sorting nexins family of proteins (SNXs) plays pleiotropic functions in protein trafficking and intracellular signaling and has been associated with several disorders, namely Alzheimer’s disease and Down’s syndrome. Despite the growing association of SNXs with neurodegeneration, not much is known about their function in the nervous system. The aim of this work was to use the nematode Caenorhabditis elegans that encodes in its genome eight SNXs orthologs, to dissect the role of distinct SNXs, particularly in the nervous system. By screening the C. elegans SNXs deletion mutants for morphological, developmental and behavioral alterations, we show here that snx-3 gene mutation leads to an array of developmental defects, such as delayed hatching, decreased brood size and life span and reduced body length. Additionally, ?snx-3 worms present increased susceptibility to osmotic, thermo and oxidative stress and distinct behavioral deficits, namely, a chemotaxis defect which is independent of the described snx-3 role in Wnt secretion. ?snx-3 animals also display abnormal GABAergic neuronal architecture and wiring and altered AIY interneuron structure. Pan-neuronal expression of C. elegans snx-3 cDNA in the ?snx-3 mutant is able to rescue its locomotion defects, as well as its chemotaxis toward isoamyl alcohol. Altogether, the present work provides the first in vivo evidence of the SNX-3 role in the nervous system.     

Forecasting Online Auctions via Self‐Exciting Point Processes

Modeling online auction prices is a popular research topic among statisticians and marketing analysts. Recent research mainly focuses on two directions: one is the functional data analysis (FDA) approach, in which the price–time relationship is modeled by a smooth curve, and the other is the point process approach, which directly models the arrival process of bidders and bids. In this paper, a novel model for the bid arrival process using a self‐exciting point process (SEPP) is proposed and applied to forecast auction prices. The FDA and point process approaches are linked together by using functional data analysis technique to describe the intensity of the bid arrival point process. Using the SEPP to model the bid arrival process, many stylized facts in online auction data can be captured. We also develop a simulation‐based forecasting procedure using the estimated SEPP intensity and historical bidding increment. In particular, prediction interval for the terminal price of merchandise can be constructed. Applications to eBay auction data of Harry Potter books and Microsoft Xbox show that the SEPP model provides more accurate and more informative forecasting results than traditional methods. Copyright © 2014 John Wiley & Sons, Ltd.     

Surface antigens of Plasmodium falciparum-infected erythrocytes as immune targets and malaria vaccine candidates

Understanding the targets and mechanisms of human immunity to malaria caused by Plasmodium falciparum is crucial for advancing effective vaccines and developing tools for measuring immunity and exposure in populations. Acquired immunity to malaria predominantly targets the blood stage of infection when merozoites of Plasmodium spp. infect erythrocytes and replicate within them. During the intra-erythrocytic development of P. falciparum, numerous parasite-derived antigens are expressed on the surface of infected erythrocytes (IEs). These antigens enable P. falciparum-IEs to adhere in the vasculature and accumulate in multiple organs, which is a key process in the pathogenesis of disease. IE surface antigens, often referred to as variant surface antigens, are important targets of acquired protective immunity and include PfEMP1, RIFIN, STEVOR and SURFIN. These antigens are highly polymorphic and encoded by multigene families, which generate substantial antigenic diversity to mediate immune evasion. The most important immune target appears to be PfEMP1, which is a major ligand for vascular adhesion and sequestration of IEs. Studies are beginning to identify specific variants of PfEMP1 linked to disease pathogenesis that may be suitable for vaccine development, but overcoming antigenic diversity in PfEMP1 remains a major challenge. Much less is known about other surface antigens, or antigens on the surface of gametocyte-IEs, the effector mechanisms that mediate immunity, and how immunity is acquired and maintained over time; these are important topics for future research.     

Glutamine deprivation initiates reversible assembly of mammalian rods and rings

Rods and rings (RR) are protein assemblies composed of cytidine triphosphate synthetase type 1 (CTPS1) and inosine monophosphate dehydrogenase type 2 (IMPDH2), key enzymes in CTP and GTP biosynthesis. Small-molecule inhibitors of CTPS1 or IMPDH2 induce RR assembly in various cancer cell lines within 15 min to hours. Since glutamine is an essential amide nitrogen donor in these nucleotide biosynthetic pathways, glutamine deprivation was examined to determine whether it leads to RR formation. HeLa cells cultured in normal conditions did not show RR, but after culturing in media lacking glutamine, short rods (<2 μm) assembled after 24 h, and longer rods (>5 μm) formed after 48 h. Upon supplementation with glutamine or guanosine, these RR underwent almost complete disassembly within 15 min. Inhibition of glutamine synthetase with methionine sulfoximine also increased RR assembly in cells deprived of glutamine. Taken together, our data support the hypothesis that CTP/GTP biosynthetic enzymes polymerize to form RR in response to a decreased intracellular level of glutamine. We speculate that rod and ring formation is an adaptive metabolic response linked to disruption of glutamine homeostasis.     

Reverse breeding in Arabidopsis thaliana generates homozygous parental lines from a heterozygous plant

Traditionally, hybrid seeds are produced by crossing selected inbred lines. Here we provide a proof of concept for reverse breeding, a new approach that simplifies meiosis such that homozygous parental lines can be generated from a vigorous hybrid individual. We silenced DMC1, which encodes the meiotic recombination protein DISRUPTED MEIOTIC cDNA1, in hybrids of A. thaliana, so that non-recombined parental chromosomes segregate during meiosis. We then converted the resulting gametes into adult haploid plants, and subsequently into homozygous diploids, so that each contained half the genome of the original hybrid. From 36 homozygous lines, we selected 3 (out of 6) complementing parental pairs that allowed us to recreate the original hybrid by intercrossing. In addition, this approach resulted in a complete set of chromosome-substitution lines. Our method allows the selection of a single choice offspring from a segregating population and preservation of its heterozygous genotype by generating homozygous founder lines.     

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

To newly identify loci for age at natural menopause, we carried out a meta-analysis of 22 genome-wide association studies (GWAS) in 38,968 women of European descent, with replication in up to 14,435 women. In addition to four known loci, we identified 13 loci newly associated with age at natural menopause (at P < 5 × 10(-8)). Candidate genes located at these newly associated loci include genes implicated in DNA repair (EXO1, HELQ, UIMC1, FAM175A, FANCI, TLK1, POLG and PRIM1) and immune function (IL11, NLRP11 and PRRC2A (also known as BAT2)). Gene-set enrichment pathway analyses using the full GWAS data set identified exoDNase, NF-κB signaling and mitochondrial dysfunction as biological processes related to timing of menopause.     

Analysis of the coding genome of diffuse large B-cell lymphoma

Diffuse large B-cell lymphoma (DLBCL) is the most common form of human lymphoma. Although a number of structural alterations have been associated with the pathogenesis of this malignancy, the full spectrum of genetic lesions that are present in the DLBCL genome, and therefore the identity of dysregulated cellular pathways, remains unknown. By combining next-generation sequencing and copy number analysis, we show that the DLBCL coding genome contains, on average, more than 30 clonally represented gene alterations per case. This analysis also revealed mutations in genes not previously implicated in DLBCL pathogenesis, including those regulating chromatin methylation (MLL2; 24% of samples) and immune recognition by T cells. These results provide initial data on the complexity of the DLBCL coding genome and identify novel dysregulated pathways underlying its pathogenesis.     

Modeling and Forecasting Online Auction Prices: A Semiparametric Regression Analysis

Interest in online auctions has been growing in recent years. There is an extensive literature on this topic, whereas modeling online auction price process constitutes one of the most active research areas. Most of the research, however, only focuses on modeling price curves, ignoring the bidding process. In this paper, a semiparametric regression model is proposed to model the online auction process. This model captures two main features of online auction data: changing arrival rates of bidding processes and changing dynamics of prices. A new inference procedure using B‐splines is also established for parameter estimation. The proposed model is used to forecast the price of an online auction. The advantage of this proposed approach is that the price can be forecast dynamically and the prediction can be updated according to newly arriving information. The model is applied to Xbox data with satisfactory forecasting properties. Copyright © 2016 John Wiley & Sons, Ltd.     

基于平面靶标的相机内部参数标定精度分析

相机内部参数标定是实现机器视觉测量的必要环节.目前常用的标定方法有Tsai两步法、DLT方法以及基于平面标靶的张正友法等.张正友法简单易行,因而得到广泛应用,标定精度取决于平面靶标的制作精度、图像特征点坐标的提取精度、镜头畸变、靶标摆放数目以及位姿分布等.对张正友标定方法的精度进行探讨,分析各影响因素对标定精度的影响,提出基于均匀设计的思想进行靶标位姿分布的设计思想.仿真和实际测试证明,采用均匀设计的靶标布局明显提高相机内部参数标定精度.