25 research outputs found
Constraining Warm Inflation with the Cosmic Microwave Background
We discuss the spectrum of scalar density perturbations from warm inflation
when the friction coefficient in the inflaton equation is dependent on
the inflaton field. The spectral index of scalar fluctuations depends on a new
slow-roll parameter constructed from . A numerical integration of the
perturbation equations is performed for a model of warm inflation and gives a
good fit to the WMAP data for reasonable values of the model's parameters.Comment: 6 pages, 2 figures, RevTeX
Performance of distributed PV in the UK: a statistical analysis of over 7000 systems
In June 2015, the UK fleet of solar photovoltaic (PV) systems reached 7.8 GWp of capacity, but there are wide gaps in our understanding of the performance of these systems, which has lead to the conservative limit of 10 GWp being imposed on UK PV capacity by the Department of Energy and Climate Change. Here we present the results of a statistical analysis of real world UK PV systems which donate data to the Microgen Database, of which there are over 7000. The mean yearly-integrated Performance Ratio (PR) of domestic scale UK PV is 83% with a standard deviation of 7%. By considering yearly-integrated PR, we have shown that 4.1 % of systems suffered long-term underperformance relative to their nominal efficiencies during 2013. The mean degradation rate for crystalline Siliconbased PV systems in the UK is -0.8 ± 0.1% per year. The state-of-the-art of UK PV, in terms of technology, manufacturing, and installation-standards, is found to have increased by 1% per year between 2002 and 2013
Large non-Gaussianity from two-component hybrid inflation
We study the generation of non-Gaussianity in models of hybrid inflation with
two inflaton fields, (2-brid inflation). We analyse the region in the parameter
and the initial condition space where a large non-Gaussianity may be generated
during slow-roll inflation which is generally characterised by a large f_NL,
tau_NL and a small g_NL. For certain parameter values we can satisfy
tau_NL>>f_NL^2. The bispectrum is of the local type but may have a significant
scale dependence. We show that the loop corrections to the power spectrum and
bispectrum are suppressed during inflation, if one assume that the fields
follow a classical background trajectory. We also include the effect of the
waterfall field, which can lead to a significant change in the observables
after the waterfall field is destabilised, depending on the couplings between
the waterfall and inflaton fields.Comment: 16 pages, 6 figures; v2: comments and references added, typos
corrected, matches published versio
A review of energy systems models in the UK: Prevalent usage and categorisation
In this paper, a systematic review of academic literature and policy papers since 2008 is undertaken with an aim of identifying the prevalent energy systems models and tools in the UK. A list of all referenced models is presented and the literature is analysed with regards sectoral coverage and technological inclusion, as well as mathematical structure of models. The paper compares available models using an appropriate classification schema, the introduction of which is aimed at making the model landscape more accessible and perspicuous, thereby enhancing the diversity of models within use. The distinct classification presented in this paper comprises three sections, which specify the model purpose and structure, technological detail and mathematical approach. The schema is not designed to be comprehensive, but rather to be a broad classification with pertinent level of information required to differentiate between models. As an example, the UK model landscape is considered and 22 models are classified in three tables, as per the proposed schema
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
A locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. Here we analyse 438 SNPs in this region in 46,451 BC and 15,438 OC cases, 15,252 BRCA1 mutation carriers and 73,444 controls and identify 13 candidate causal SNPs associated with serous OC (P=9.2 × 10-20), ER-negative BC (P=1.1 × 10-13), BRCA1-associated BC (P=7.7 × 10-16) and triple negative BC (P-diff=2 × 10-5). Genotype-gene expression associations are identified for candidate target genes ANKLE1 (P=2 × 10-3) and ABHD8 (P<2 × 10-3). Chromosome conformation capture identifies interactions between four candidate SNPs and ABHD8, and luciferase assays indicate six risk alleles increased transactivation of the ADHD8 promoter. Targeted deletion of a region containing risk SNP rs56069439 in a putative enhancer induces ANKLE1 downregulation; and mRNA stability assays indicate functional effects for an ANKLE1 3′-UTR SNP. Altogether, these data suggest that multiple SNPs at 19p13 regulate ABHD8 and perhaps ANKLE1 expression, and indicate common mechanisms underlying breast and ovarian cancer risk
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-modifying loci, we performed a multi-stage GWAS of 11,705 BRCA1 carriers (of whom 5,920 were diagnosed with breast and 1,839 were diagnosed with ovarian cancer), with a further replication in an additional sample of 2,646 BRCA1 carriers. We identified a novel breast cancer risk modifier locus at 1q32 for BRCA1 carriers (rs2290854, P = 2.7×10-8, HR = 1.14, 95% CI: 1.09-1.20). In addition, we identified two novel ovarian cancer risk modifier loci: 17q21.31 (rs17631303, P = 1.4×10-8, HR = 1.27, 95% CI: 1.17-1.38) and 4q32.3 (rs4691139, P = 3.4×10-8, HR = 1.20, 95% CI: 1.17-1.38). The 4q32.3 locus was not associated with ovarian cancer risk in the general population or BRCA2 carriers, suggesting a BRCA1-specific associat
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors. About 50 common variants have been shown to modify BC risk for mutation carriers. All but three, were identified in general population studies. Other mutation carrier-specific susceptibility variants may exist but studies of mutation carriers have so far been underpowered. We conduct a novel case-only genome-wide association study comparing genotype frequencies between 60,212 general population BC cases and 13,007 cases with BRCA1 or BRCA2 mutations. We identify robust novel associations for 2 variants with BC for BRCA1 and 3 for BRCA2 mutation carriers, P < 10−8, at 5 loci, which are not associated with risk in the general population. They include rs60882887 at 11p11.2 where MADD, SP11 and EIF1, genes previously implicated in BC biology, are predicted as potential targets. These findings will contribute towards customising BC polygenic risk scores for BRCA1 and BRCA2 mutation carriers