68 research outputs found

    Calibration in a Data Sparse Environment: How Many Cases Did We Miss?

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    Reported case numbers in the COVID-19 pandemic are assumed in many countries to have underestimated the true prevalence of the disease. Deficits in reporting may have been particularly great in countries with limited testing capability and restrictive testing policies. Simultaneously, some models have been accused of over-reporting the scale of the pandemic. At a time when modeling consortia around the world are turning to the lessons learnt from pandemic modelling, we present an example of simulating testing as well as the spread of disease. In particular, we factor in the amount and nature of testing that was carried out in the first wave of the COVID-19 pandemic (March - September 2020), calibrating our spatial Agent Based Model (ABM) model to the reported case numbers in Zimbabwe

    Scale matters: Variations in spatial and temporal patterns of epidemic outbreaks in agent-based models

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    Agent-based modellers frequently make use of techniques to render simulated populations more computationally tractable on actionable timescales. Many generate a relatively small number of “representative” agents, each of which is “scaled up” to represent some larger number of individuals involved in the system being studied. The degree to which this “scaling” has implications for model forecasts is an underdeveloped field of study; in particular, there has been little known research on the spatial implications of such techniques. This work presents a case study of the impact of the simulated population size, using a model of the spread of COVID-19 among districts in Zimbabwe for the underlying system being studied. The impact of the relative scale of the population is explored in conjunction with the spatial setup, and crucial model parameters are varied to highlight where scaled down populations can be safely used and where modellers should be cautious. The results imply that in particular, different geographical dynamics of the spread of disease are associated with varying population sizes, with implications for researchers seeking to use scaled populations in their research. This article is an extension on work previously presented as part of the International Conference on Computational Science 2022 (Wise et al., 2022)[1]

    Mycorrhizal colonisation in roots of Holcus lanatus (Yorkshire Fog) in a permanent pasture under conditions of reduced precipitation

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    The UK climate is projected to become warmer, with more frequent hotter, drier summers. Many governments and international organisations are concerned about how climate change will affect food production and security. Mycorrhizal fungi are an essential part of agricultural systems and yet little is known about how climate change will affect mycorrhizal fungi. We investigated the effect of reduced precipitation on levels of arbuscular mycorrhizal (AM) colonisation in the top 10 cm of soil in the grass Holcus lanatus L. (Yorkshire Fog) in a permanent pasture in South Gloucestershire, UK. Incident rainfall was reduced, by approximately 50%, using clear gutters supported on steel frames. Over three growing seasons we observed little difference in levels of AM colonisation and numbers of intra-root fungal structures between the roots of H. lanatus grown with reduced or full incident rainfall. Time of year when water stress occurred had a stronger effect on levels of colonisation than the absolute amount of precipitation received. In H. lanatus, growing in a permanent pasture, levels of AM colonisation were around 40%-50%, across a range of precipitation, from 18% above to 36% below the long-term average. The results highlight the complex relationships between mycorrhizal fungi, host plant, and abiotic stress

    Construction and EST sequencing of full-length, drought stress cDNA libraries for common beans (Phaseolus vulgaris L.)

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    <p>Abstract</p> <p>Background</p> <p>Common bean is an important legume crop with only a moderate number of short expressed sequence tags (ESTs) made with traditional methods. The goal of this research was to use full-length cDNA technology to develop ESTs that would overlap with the beginning of open reading frames and therefore be useful for gene annotation of genomic sequences. The library was also constructed to represent genes expressed under drought, low soil phosphorus and high soil aluminum toxicity. We also undertook comparisons of the full-length cDNA library to two previous non-full clone EST sets for common bean.</p> <p>Results</p> <p>Two full-length cDNA libraries were constructed: one for the drought tolerant Mesoamerican genotype BAT477 and the other one for the acid-soil tolerant Andean genotype G19833 which has been selected for genome sequencing. Plants were grown in three soil types using deep rooting cylinders subjected to drought and non-drought stress and tissues were collected from both roots and above ground parts. A total of 20,000 clones were selected robotically, half from each library. Then, nearly 10,000 clones from the G19833 library were sequenced with an average read length of 850 nucleotides. A total of 4,219 unigenes were identified consisting of 2,981 contigs and 1,238 singletons. These were functionally annotated with gene ontology terms and placed into KEGG pathways. Compared to other EST sequencing efforts in common bean, about half of the sequences were novel or represented the 5' ends of known genes.</p> <p>Conclusions</p> <p>The present full-length cDNA libraries add to the technological toolbox available for common bean and our sequencing of these clones substantially increases the number of unique EST sequences available for the common bean genome. All of this should be useful for both functional gene annotation, analysis of splice site variants and intron/exon boundary determination by comparison to soybean genes or with common bean whole-genome sequences. In addition the library has a large number of transcription factors and will be interesting for discovery and validation of drought or abiotic stress related genes in common bean.</p

    Research students exhibition catalogue 2011

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    The catalogue demonstrates the scope and vibrancy of current inquiries and pays tribute to the creative capacity and investment of UCA research students. It brings together contributions from students who are at different stages in their research ad/venture. Their explorations are connected by the centrality of contemporary material practices as focal point for the reconsideration of societal values, cultural symbols and rituals and their meaning, and the trans/formation of individual, collective and national identities The media and formats employed range from cloth, jewellery and ceramics to analogue film, the human voice and the representation of dress and fashionin virtual environments. Thematic interests span from explorations at the interface of art and medical science to an investigation of the role of art in contested spaces, or the role of metonymy in ‘how the arts think’ And whilst the projects are motivated by personal curiosity and passion, their outcomes transcend the boundaries of individual practice and offer new insights, under-standing and applications for the benefit of wider society. Prof. Kerstin Me

    Red clover (Trifolium pratense L.) draft genome provides a platform for trait improvement

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    Red clover (Trifolium pratense L.) is a globally significant forage legume in pastoral livestock farming systems. It is an attractive component of grassland farming, because of its high yield and protein content, nutritional value and ability to fix atmospheric nitrogen. Enhancing its role further in sustainable agriculture requires genetic improvement of persistency, disease resistance, and tolerance to grazing. To help address these challenges, we have assembled a chromosome-scale reference genome for red clover. We observed large blocks of conserved synteny with Medicago truncatula and estimated that the two species diverged ~23 million years ago. Among the 40,868 annotated genes, we identified gene clusters involved in biochemical pathways of importance for forage quality and livestock nutrition. Genotyping by sequencing of a synthetic population of 86 genotypes show that the number of markers required for genomics-based breeding approaches is tractable, making red clover a suitable candidate for association studies and genomic selection

    Psychology Meets Biology in COVID-19: What We Know and Why It Matters for Public Health

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    Psychosocial factors are related to immune, viral, and vaccination outcomes. Yet, this knowledge has been poorly represented in public health initiatives during the COVID-19 pandemic. This review provides an overview of biopsychosocial links relevant to COVID-19 outcomes by describing seminal evidence about these associations known prepandemic as well as contemporary research conducted during the pandemic. This focuses on the negative impact of the pandemic on psychosocial health and how this in turn has likely consequences for critically relevant viral and vaccination outcomes. We end by looking forward, highlighting the potential of psychosocial interventions that could be leveraged to support all people in navigating a postpandemic world and how a biopsychosocial approach to health could be incorporated into public health responses to future pandemics

    The Consensus Coding Sequence (Ccds) Project: Identifying a Common Protein-Coding Gene Set for the Human and Mouse Genomes

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    Effective use of the human and mouse genomes requires reliable identification of genes and their products. Although multiple public resources provide annotation, different methods are used that can result in similar but not identical representation of genes, transcripts, and proteins. The collaborative consensus coding sequence (CCDS) project tracks identical protein annotations on the reference mouse and human genomes with a stable identifier (CCDS ID), and ensures that they are consistently represented on the NCBI, Ensembl, and UCSC Genome Browsers. Importantly, the project coordinates on manually reviewing inconsistent protein annotations between sites, as well as annotations for which new evidence suggests a revision is needed, to progressively converge on a complete protein-coding set for the human and mouse reference genomes, while maintaining a high standard of reliability and biological accuracy. To date, the project has identified 20,159 human and 17,707 mouse consensus coding regions from 17,052 human and 16,893 mouse genes. Three evaluation methods indicate that the entries in the CCDS set are highly likely to represent real proteins, more so than annotations from contributing groups not included in CCDS. The CCDS database thus centralizes the function of identifying well-supported, identically-annotated, protein-coding regions.National Human Genome Research Institute (U.S.) (Grant number 1U54HG004555-01)Wellcome Trust (London, England) (Grant number WT062023)Wellcome Trust (London, England) (Grant number WT077198
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