39 research outputs found
Qualitative System Identification from Imperfect Data
Experience in the physical sciences suggests that the only realistic means of
understanding complex systems is through the use of mathematical models.
Typically, this has come to mean the identification of quantitative models
expressed as differential equations. Quantitative modelling works best when the
structure of the model (i.e., the form of the equations) is known; and the
primary concern is one of estimating the values of the parameters in the model.
For complex biological systems, the model-structure is rarely known and the
modeler has to deal with both model-identification and parameter-estimation. In
this paper we are concerned with providing automated assistance to the first of
these problems. Specifically, we examine the identification by machine of the
structural relationships between experimentally observed variables. These
relationship will be expressed in the form of qualitative abstractions of a
quantitative model. Such qualitative models may not only provide clues to the
precise quantitative model, but also assist in understanding the essence of
that model. Our position in this paper is that background knowledge
incorporating system modelling principles can be used to constrain effectively
the set of good qualitative models. Utilising the model-identification
framework provided by Inductive Logic Programming (ILP) we present empirical
support for this position using a series of increasingly complex artificial
datasets. The results are obtained with qualitative and quantitative data
subject to varying amounts of noise and different degrees of sparsity. The
results also point to the presence of a set of qualitative states, which we
term kernel subsets, that may be necessary for a qualitative model-learner to
learn correct models. We demonstrate scalability of the method to biological
system modelling by identification of the glycolysis metabolic pathway from
data
Localities of Memory, Localities of Mobilisation: British Military Communities and the Great War, 1919-1939
PhDThis thesis examines the role of British localities in the production of military force during the 1920s and 1930s. I argue that, during an era so disenfranchising for the armed forces in national politics and culture, the âLocalâ provided a haven for servicemen and military units. Rather than theorising mobilisation as a set of state centred economic or technocratic proscriptions, this research takes the social and cultural renewal of military units as a starting point.
Drawing on a range of historical and anthropological methodologies, I have set out to uncover what were â to borrow Foucaultâs phrase â âregimes of truthâ: multiple ideological currents and social contexts that legitimised service identities during this period. Local spaces are not only useful arenas for dissecting these operations; local people and identities were crucial formative elements in these processes. Two case studies have provided the ground for this investigation:
Newcastle and Glasgow. The thesis dissects the body of the British military machine at these entry points, viewing the configuration of military and naval
power at ground level and the emergence of manpower from the collision between state directives and local society. It also examines the communities (soldiers, veterans) that arose through this. Focus moves from military to urban spaces, revealing the characters (pressmen, politicians) and practices (sociability, ritual, performance) that legitimised these communities. Much of this cultural
work evoked the memory of the Great War and here the thesis intervenes in academic debates surrounding Commemoration after 1918. The final chapter unites these perspectives in a chronological elaboration of the period 1935-1939, detailing the ground level effort for national and civil defence. As well as enlivening our understanding of 20th century mobilisation, this research explores the depths of British local and national identities and the intricate ways in which the armed forces were framed within both.AHRC
Queen Mary Central Research Fund and the Stretton Fund
The Henkel Foundation Scholarship, awarded by the
International Research Centre of the Historia de la Grande Guerre in 201
Genomic diversity in naturally transformable Streptococcus pneumoniae
Infections due to Streptococcus pneumoniae (the pneumococcus) remain a substantial source of morbidity and mortality in both developing and developed countries despite a century of research and the development of effective therapeutic interventions (such as antibiotic therapy and vaccination). The ability of the pneumococcus to evade multiple classes of antibiotic through several genetically determined resistance mechanisms and its evasion of capsular polysaccharide based vaccines through serotype replacement and capsular switching, all reflect the extensive diversity and plasticity of the genome of this naturally transformable organism which can readily alter its genome in response to its environment and the pressures placed upon it in order to survive.
The purpose of this thesis is to investigate this diversity from a genome sequence perspective and to relate these observations to pneumococcal molecular epidemiology in a region of high biodiversity, the pathogenesis of certain disease manifestations and assess for a possible bacterial genetic basis for the pneumococcal phenotypes of, âcarriageâ and, âinvasion.â
In order to do this, microarray comparative genomic hybridization (CGH) has been utilized to compare DNA from a variety of pneumococcal isolates chosen from 10 diverse serotypes and Multilocus Sequence Types and from clinically relevant serotypes and sequence types (particularly serotypes 3, 4 and 14 and sequence types ST9, ST246 and ST180)) against a reference, sequenced pneumococcal genome from an extensively investigated serotype 4 isolate â TIGR4.
Microarray comparison of the transcriptional profiles of several isolates has also been undertaken to compare gene expression from isolates of serotype 1 (ST227 and ST306) and serotype 3 (ST180) related to particular disease states and exposure of a multi-resistant pneumococcus to an antimicrobial (clarithromycin) commonly used to treat pneumococcal pneumonia
Preparation and characterization of a protein extract from date palm fruit (Phoenix dactylifera L.) : investigation of nutritional and functional properties
The worldâs population will reach 9 billion by 2050, increasing the pressure to find
alternative protein sources to animal protein. The high global demand for soy protein
ingredients has resulted in tropical deforestation which is associated with adverse
health impact, agronomic, environmental and climate damage and there is a need to
find alternative plant protein sources to soy protein. The Kingdom of Saudi Arabia
(KSA) is considered as the second largest producer of date palm fruit among the
current date-producing countries, resulting also in significant quantities of dates going
to waste. The aims of this study were to develop a process for extraction of protein
from date fruit suitable to be implemented in the food industry, to characterise the
proteinâs electrophoretic profile by sodium dodecyl sulphate-polyacrylamide gel
electrophoresis (SDS-PAGE), to identify the proteins by Liquid-Chromatography
Coupled Tandem Mass Spectrometry (LC-MS/MS), to study the physicochemical and
functional properties of date fruit protein extract (DFPE) and the effect of thermal
treatment, to determine the chemical composition, nutritional value, anti-nutritional
factors and anti-oxidant properties and to develop an infant cereal with reduced
allergenicity.
Proximate and mineral analysis, anti-oxidant, amino acid composition and digestibility
analysis of DFPE, reported in Chapter 2 showed that the protein extract contains all
essential amino acids, is a high source of iron and has excellent anti-oxidant properties
matching that of ascorbic acid. The extract had a lower protein digestibility-corrected
amino acid score (PDCAAS) value than soy protein isolate (SPI) and contained anti nutritional factors e.g. oxalate, tannin and phytate, yet at low quantities that is assumed
not to be of anti-nutritional concern. Physicochemical and functional properties of the extract and the respective effect of
thermal treatment are reported in Chapter 3. The concentration of free and total
sulphydryl groups (FSH and TSH) were significantly less that for SPI, confirming the
results of low cysteine in the amino acid analysis of DFPE. The effect of thermal
treatment on the profile of sulphydryl (SH) groups indicates that DFPE is less
thermally stable than SPI, whilst considering the fact that DFPE had been subjected to
heat treatment during the extraction process. This physicochemical profile was
mirrored by the corresponding decrease in functionality including decreases after
longer heating times in solubility, foam capacity emulsion stability index and increased
water separation in emulsions.
Chapter 4 describes the development of a protein extract containing 25.8% protein
per dry weight using a new extraction process, which is a 13-fold enrichment compared
to the 2.8% in the initial sample. The extraction process resulted in 4.2% DFPE, 57.2%
date syrup and 38.6% waste. DFPE contains 50% protein whereas the remainder was
in the date syrup (26.7%) and in the waste (24.3%) which could also be lost due to
protease activity. The electrophoretic profile was established. LC-MS/MS results
indicated the two most abundant proteins to be sorbitol dehydrogenase-like with MW
(kDa) 39, an energy-related protein and catalase isozyme 2 with MW (kDa) 57, a
disease/defense-related protein.
Chapter 5 describes the development of an infant cereal based on date fruit protein as
a potential competitor to a commercial infant cereal (CERELAC) sold in the KSA. The
date cereal product lacked certain amino acids and calcium and contained low levels
of oxalate, phytate and tannin. A date-cereal porridge prepared with camel milk had a
proximate and mineral composition matching that of a porridge made with CERELAC
prepared with cowâs milk apart from lacking fat, calcium and selenium, resulting in a
product with reduced allergenicity to gluten and cowâs milk. DFPE could add to the rising need to find replacement for soy protein because the expansion of soy bean
production and consumption is associated with environmental threats, such as
deforestation
Genomic diversity in naturally transformable Streptococcus pneumoniae
Infections due to Streptococcus pneumoniae (the pneumococcus) remain a substantial source of morbidity and mortality in both developing and developed countries despite a century of research and the development of effective therapeutic interventions (such as antibiotic therapy and vaccination). The ability of the pneumococcus to evade multiple classes of antibiotic through several genetically determined resistance mechanisms and its evasion of capsular polysaccharide based vaccines through serotype replacement and capsular switching, all reflect the extensive diversity and plasticity of the genome of this naturally transformable organism which can readily alter its genome in response to its environment and the pressures placed upon it in order to survive. The purpose of this thesis is to investigate this diversity from a genome sequence perspective and to relate these observations to pneumococcal molecular epidemiology in a region of high biodiversity, the pathogenesis of certain disease manifestations and assess for a possible bacterial genetic basis for the pneumococcal phenotypes of, âcarriageâ and, âinvasion.â In order to do this, microarray comparative genomic hybridization (CGH) has been utilized to compare DNA from a variety of pneumococcal isolates chosen from 10 diverse serotypes and Multilocus Sequence Types and from clinically relevant serotypes and sequence types (particularly serotypes 3, 4 and 14 and sequence types ST9, ST246 and ST180)) against a reference, sequenced pneumococcal genome from an extensively investigated serotype 4 isolate â TIGR4. Microarray comparison of the transcriptional profiles of several isolates has also been undertaken to compare gene expression from isolates of serotype 1 (ST227 and ST306) and serotype 3 (ST180) related to particular disease states and exposure of a multi-resistant pneumococcus to an antimicrobial (clarithromycin) commonly used to treat pneumococcal pneumonia.EThOS - Electronic Theses Online ServiceGBUnited Kingdo