105 research outputs found
Quality of Service Model on Data Link Layer for Mission Critical Traffic on IEEE 802.11g Networks in Infrastructure Mode
No full textThis article presents a synthesized review as state of the art of the study of QoS for mission-critical traffic in wireless local area networks that use the IEEE 802.11g protocol. This is to highlight previous research for their contribution will constitute a reference to guide a proposed new approach to ensuring the quality of service for this type of traffic using the above protocol. The review is based on academic and business items made during the current five years. As a result of this review it is evident that there have been many efforts to address the issue but there are still gaps in the characterization of mission-critical traffic and ensuring quality of service for the same, due the new applications and the large host of WiFi networks in business and government, which has led to increased demand for access channels and, therefore, a challenge to the progress already known, such as IEEE 802.1q.</p
Modelo de Calidad de Servicio a Nivel de Enlace de Datos para Tráfico de Misión Crítica sobre Redes IEEE 802.11g en Modo Infraestructura
No full textThis article presents a synthesized review as state of the art of the study of QoS for mission-critical traffic in wireless local area networks that use the IEEE 802.11g protocol. This is to highlight previous research for their contribution will constitute a reference to guide a proposed new approach to ensuring the quality of service for this type of traffic using the above protocol. The review is based on academic and business items made during the current five years. As a result of this review it is evident that there have been many efforts to address the issue but there are still gaps in the characterization of mission-critical traffic and ensuring quality of service for the same, due the new applications and the large host of WiFi networks in business and government, which has led to increased demand for access channels and, therefore, a challenge to the progress already known, such as IEEE 802.1q.Este artículo presenta en forma sintetizada una revisión del estado del arte del estudio de la Calidad de Servicio para tráfico de misión crítica en redes de área local inalámbricas que utilizan el protocolo IEEE 802.11g. Esto con el fin de resaltar investigaciones previas que por su aporte se constituyan en un referente para orientar la propuesta de una nueva forma de abordar el aseguramiento de la calidad de servicio para este tipo de tráfico utilizando el protocolo mencionado. La revisión se basa en artículos académicos y empresariales elaborados durante el presente lustro. Como resultado de dicha revisión se evidencia que han sido muchos los esfuerzos para abordar el tema pero aún existen vacíos en la caracterización del tráfico de misión crítica y la garantía de la calidad del servicio para el mismo, debido a las nuevas aplicaciones informáticas y a la gran acogida de las redes WiFi en el ámbito empresarial y gubernamental; lo que ha generado un aumento en la demanda de los canales de acceso y, por ende, un desafío para los avances ya conocidos en la materia, tal como IEEE 802.1q
Diseño de una solución de nube privada para las prácticas académicas en el programa de ingeniería de telecomunicaciones de la usta, sede bogotá.
No full textEste estudio se propone diseñar una Nube Privada en el programa Ingeniería de Telecomunicaciones basada en un servidor físico (solución on-premises). Esta alternativa busca mejorar la calidad educativa mediante una infraestructura tecnológica controlada y personalizada, frente a opciones de nubes públicas como Azure o AWS, además de reducir costos operativos. Se analizan los beneficios y desafíos de esta implementación, enfatizando su capacidad para optimizar el aprendizaje y fomentar la innovación educativaThis study aims to design and implement a Private Cloud in the Telecommunications Engineering Faculty based on a physical server (on-premises solution). This alternative seeks to improve educational quality through a controlled and customized technological infrastructure, compared to public cloud options like Azure or AWS. In addition to reducing operational costs, the benefits and challenges of this implementation are analyzed, emphasizing its ability to optimize learning and foster educational innovationIngeniero de TelecomunicacionesPregrad
Hundreds of variants clustered in genomic loci and biological pathways affect human height
No full textMost common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence the phenotype. Genome-wide association (GWA) studies have identified more than 600 variants associated with human traits(1), but these typically explain small fractions of phenotypic variation, raising questions about the use of further studies. Here, using 183,727 individuals, we show that hundreds of genetic variants, in at least 180 loci, influence adult height, a highly heritable and classic polygenic trait(2,3). The large number of loci reveals patterns with important implications for genetic studies of common human diseases and traits. First, the 180 loci are not random, but instead are enriched for genes that are connected in biological pathways (P = 0.016) and that underlie skeletal growth defects (P<0.001). Second, the likely causal gene is often located near the most strongly associated variant: in 13 of 21 loci containing a known skeletal growth gene, that gene was closest to the associated variant. Third, at least 19 loci have multiple independently associated variants, suggesting that allelic heterogeneity is a frequent feature of polygenic traits, that comprehensive explorations of already-discovered loci should discover additional variants and that an appreciable fraction of associated loci may have been identified. Fourth, associated variants are enriched for likely functional effects on genes, being over-represented among variants that alter amino-acid structure of proteins and expression levels of nearby genes. Our data explain approximately 10% of the phenotypic variation in height, and we estimate that unidentified common variants of similar effect sizes would increase this figure to approximately 16% of phenotypic variation (approximately 20% of heritable variation). Although additional approaches are needed to dissect the genetic architecture of polygenic human traits fully, our findings indicate that GWA studies can identify large numbers of loci that implicate biologically relevant genes and pathways
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
No full textCorrection to: Nature Genetics https://doi.org/10.1038/ng.3668, published online 26 September 2016.
In the version of the article published, the surname of author Aaron Isaacs is misspelled as Issacs
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
No full textApproaches exploiting trait distribution extremes may be used to identify loci associated with common traits, but it is unknown whether these loci are generalizable to the broader population. In a genome-wide search for loci associated with the upper versus the lower 5th percentiles of body mass index, height and waist-to-hip ratio, as well as clinical classes of obesity, including up to 263,407 individuals of European ancestry, we identified 4 new loci (IGFBP4, H6PD, RSRC1 and PPP2R2A) influencing height detected in the distribution tails and 7 new loci (HNF4G, RPTOR, GNAT2, MRPS33P4, ADCY9, HS6ST3 and ZZZ3) for clinical classes of obesity. Further, we find a large overlap in genetic structure and the distribution of variants between traits based on extremes and the general population and little etiological heterogeneity between obesity subgroups
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
No full textObesity is globally prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity susceptibility, we examined associations between body mass index and similar to 2.8 million SNPs in up to 123,865 individuals with targeted follow up of 42 SNPs in up to 125,931 additional individuals. We confirmed 14 known obesity susceptibility loci and identified 18 new loci associated with body mass index (P < 5 x 10(-8)), one of which includes a copy number variant near GPRC5B. Some loci (at MC4R, POMC, SH2B1 and BDNF) map near key hypothalamic regulators of energy balance, and one of these loci is near GIPR, an incretin receptor. Furthermore, genes in other newly associated loci may provide new insights into human body weight regulation
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
No full textWaist-hip ratio (WHR) is a measure of body fat distribution and a predictor of metabolic consequences independent of overall adiposity. WHR is heritable, but few genetic variants influencing this trait have been identified. We conducted a meta-analysis of 32 genome-wide association studies for WHR adjusted for body mass index (comprising up to 77,167 participants), following up 16 loci in an additional 29 studies (comprising up to 113,636 subjects). We identified 13 new loci in or near RSPO3, VEGFA, TBX15-WARS2, NFE2L3, GRB14, DNM3-PIGC, ITPR2-SSPN, LY86, HOXC13, ADAMTS9, ZNRF3-KREMEN1, NISCH-STAB1 and CPEB4 (P = 1.9 × 10⁻⁹ to P = 1.8 × 10⁻⁴⁰) and the known signal at LYPLAL1. Seven of these loci exhibited marked sexual dimorphism, all with a stronger effect on WHR in women than men (P for sex difference = 1.9 × 10⁻³ to P = 1.2 × 10⁻¹³). These findings provide evidence for multiple loci that modulate body fat distribution independent of overall adiposity and reveal strong gene-by-sex interactions
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
No full textTo identify genetic variants associated with birth weight, we meta-analyzed six genome-wide association (GWA) studies (n = 10,623 Europeans from pregnancy/birth cohorts) and followed up two lead signals in 13 replication studies (n = 27,591). rs900400 near LEKR1 and CCNL1 (P = 2 x 10(-35)) and rs9883204 in ADCY5 (P = 7 x 10(-15)) were robustly associated with birth weight. Correlated SNPs in ADCY5 were recently implicated in regulation of glucose levels and susceptibility to type 2 diabetes, providing evidence that the well-described association between lower birth weight and subsequent type 2 diabetes has a genetic component, distinct from the proposed role of programming by maternal nutrition. Using data from both SNPs, we found that the 9% of Europeans carrying four birth weight-lowering alleles were, on average, 113 g (95% CI 89-137 g) lighter at birth than the 24% with zero or one alleles (P(trend) = 7 x 10(-30)). The impact on birth weight is similar to that of a mother smoking 4-5 cigarettes per day in the third trimester of pregnancy
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
No full textThe phenotypic effect of some single nucleotide polymorphisms (SNPs) depends on their parental origin. We present a novel approach to detect parent-of-origin effects (POEs) in genome-wide genotype data of unrelated individuals. The method exploits increased phenotypic variance in the heterozygous genotype group relative to the homozygous groups. We applied the method to >56,000 unrelated individuals to search for POEs influencing body mass index (BMI). Six lead SNPs were carried forward for replication in five family-based studies (of ~4,000 trios). Two SNPs replicated: the paternal rs2471083-C allele (located near the imprinted KCNK9 gene) and the paternal rs3091869-T allele (located near the SLC2A10 gene) increased BMI equally (beta = 0.11 (SD), P<0.0027) compared to the respective maternal alleles. Real-time PCR experiments of lymphoblastoid cell lines from the CEPH families showed that expression of both genes was dependent on parental origin of the SNPs alleles (P<0.01). Our scheme opens new opportunities to exploit GWAS data of unrelated individuals to identify POEs and demonstrates that they play an important role in adult obesity. © 2014 Hoggart et al
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