Relevant bibliographies by topics / High throughput imaging

Academic literature on the topic 'High throughput imaging'

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Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "High throughput imaging"

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Knott, G., D. Wall, and B. Lich. "High-Throughput 3D Cellular Imaging." Microscopy and Microanalysis 15, S2 (July 2009): 934–35. http://dx.doi.org/10.1017/s1431927609097037.

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Golding, Stephen J. "High-throughput magnetic resonance imaging." Academic Radiology 3 (April 1996): S53. http://dx.doi.org/10.1016/s1076-6332(96)80483-1.

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Enderlein, Jörg. "Single-molecule imaging goes high throughput." Nature Nanotechnology 15, no. 6 (April 20, 2020): 419–20. http://dx.doi.org/10.1038/s41565-020-0676-7.

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Su, Justin, Liang Xu, Derek Tseng, and Aydogan Ozcan. "High-throughput 3D imaging of sperm." Molecular Reproduction and Development 80, no. 4 (March 13, 2013): 243. http://dx.doi.org/10.1002/mrd.22159.

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Stavrakis, Stavros, Gregor Holzner, Jaebum Choo, and Andrew deMello. "High-throughput microfluidic imaging flow cytometry." Current Opinion in Biotechnology 55 (February 2019): 36–43. http://dx.doi.org/10.1016/j.copbio.2018.08.002.

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Ogata, Koretsugu. "High Throughput MALDI MS Imaging Using Imaging Mass Microscope." Journal of the Mass Spectrometry Society of Japan 69, no. 5 (October 1, 2021): 145–46. http://dx.doi.org/10.5702/massspec.s21-28.

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McDonnell, Liam A., Alexandra van Remoortere, René J. M. van Zeijl, Hans Dalebout, Marco R. Bladergroen, and André M. Deelder. "Automated imaging MS: Toward high throughput imaging mass spectrometry." Journal of Proteomics 73, no. 6 (April 2010): 1279–82. http://dx.doi.org/10.1016/j.jprot.2009.10.011.

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Brown, V. M. "High-Throughput Imaging of Brain Gene Expression." Genome Research 12, no. 2 (February 1, 2002): 244–54. http://dx.doi.org/10.1101/gr.204102.

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Ahmed, Wamiq M., Arif Ghafoor, and J. Paul Robinson. "Knowledge Extraction for High-Throughput Biological Imaging." IEEE Multimedia 14, no. 4 (October 2007): 52–62. http://dx.doi.org/10.1109/mmul.2007.77.

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Gibbs, Phillip R., Christian S. Uehara, Peter T. Nguyen, and Richard C. Willson. "Imaging Polarimetry for High Throughput Chiral Screening." Biotechnology Progress 19, no. 4 (September 5, 2008): 1329–34. http://dx.doi.org/10.1021/bp025729l.

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Dissertations / Theses on the topic "High throughput imaging"

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Velasco, J. Cabello. "High throughput digital autoradiography imaging." Thesis, University of Surrey, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.510588.

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Cabello, Velasco J. "High throughput digital beta autoradiography imaging." Thesis, University of Surrey, 2009. http://epubs.surrey.ac.uk/844626/.

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This thesis presents three main strands of work concerned with developing digital imaging for high throughput beta autoradiography. These three strands comprise work with the image sensor technology, Monte Carlo simulation and the use of post-acquisition image analysis based on image registration. In this way, the complete autoradiography imaging chain is addressed. CCD and CMOS imaging technologies are presented as potential imaging alternatives to using conventional film in autoradiography. These digital technologies exhibit enhanced sensitivity, dynamic range and linearity compared to film using imaging methods developed at Surrey. These imaging methods address the different sources of noise typically present in CCD and CMOS technologies. Tissue imaging using 3H, 35S and 121I, the typical radioisotopes used by the Drug Addiction Group in the School of Biomedical and Biological Sciences, is presented. The first successful images of 3H-labelled tissue sections using CCD and CMOS technologies operating at room temperature are presented as one of the main achievements of this work. To better understand the image creation process some preliminary Monte Carlo simulations, using the GEANT4 toolkit, have been undertaken, demonstrating intrinsic and extrinsic key parameters of these digital sensors that can be used to optimise spatial resolution. These simulations demonstrate that each radioisotope requires a different optimum detector architecture. In this work these optimum architectures are analysed. To support the high sensitivity (i.e. fast) imaging produced by the sensor technology, automated post-acquisition analysis is also considered, using an atlas-based image registration approach, by previously aligning automatically segmented biological landmarks using a feature-based extraction approach, region growing. This has the potential to speed up the post-acquisition analysis aspects of the imaging chain. Thus a computer-based tool designed to semi-automatically elastically register a radiogram with an atlas has been developed.
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Rock, Reza M. "An Imaging Ammeter for High Throughput Electrochemical Research." Research Showcase @ CMU, 2013. http://repository.cmu.edu/dissertations/235.

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Rapid testing of electrocatalysts and corrosion resistant alloys accelerates discovery of promising new materials. Imaging amperometry, based on the deployment of colloidal particles as probes of the local current density, allows simultaneous electrochemical characterization of the entire composition space represented in a thin-film alloy "library" electrode. Previous work has shown that nanometer scale variations in particle-electrode distance for single particles in electric fields can be measured optically and translated into local current density, independent of electrical measurements. Implementation of this method to enable simultaneous measurements across non-uniform samples involves using a sparse, uniform layer of particles, which requires modification of previously existing theory and methods. Imaging individual particles for this application is infeasible at the low magnification levels needed to image an entire macroscopic (~1 square cm) sample. Mapping of electrochemical activity across the surface can be achieved nevertheless by imaging the entire electrode surface and gridding the resulting images into a mosaic of square “patch” areas 100 μm to a side, each containing 15-30 particles. The work presented in this dissertation shows that the integrated light intensity in each patch is the sum of the light scattering from all of the particles present in that patch, and that this total measured intensity can be used to infer the current density in the patch during electrochemical experiments. In addition to scaling the imaging ammeter up to ensembles of particles, the theory for translating measured particle motion to current density has been substantially improved. These improvements involve proper modeling of the current distribution on the electrode below the particles, which has a profound impact on the forces acting on each particle. This work demonstrates that the use of realistic kinetic models for the imaging ammeter is both vital and a discovered opportunity to increase its sensitivity. Finite element analysis was used to explore the variable space of the parameters involved, to better understand the impact of factors such as the current density and solution conductivity on the motion of the particles. Going forward, this information will be leveraged to improve the accuracy of the macroscopic imaging ammeter. To complete the groundwork for the imaging ammeter laid out in this thesis, proof of concept experiments using a nickel/iron composition spread alloy film were performed. In a 1×5 mm2 area containing alloy compositions from 20% iron to 100% iron, expected trends in electrochemical activity were observed during experiments, i.e. the current density as a function of voltage increased with increasing nickel content on the electrode surface. Future work will probe Fe/Ni alloy compositions with less iron, subsequently moving on to other binary and eventually ternary alloy systems.
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Cao, Hongfei. "High-throughput Visual Knowledge Analysis and Retrieval in Big Data Ecosystems." Thesis, University of Missouri - Columbia, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=13877134.

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Visual knowledge plays an important role in many highly skilled applications, such as medical diagnosis, geospatial image analysis and pathology diagnosis. Medical practitioners are able to interpret and reason about diagnostic images based on not only primitive-level image features such as color, texture, and spatial distribution but also their experience and tacit knowledge which are seldom articulated explicitly. This reasoning process is dynamic and closely related to real-time human cognition. Due to a lack of visual knowledge management and sharing tools, it is difficult to capture and transfer such tacit and hard-won expertise to novices. Moreover, many mission-critical applications require the ability to process such tacit visual knowledge in real time. Precisely how to index this visual knowledge computationally and systematically still poses a challenge to the computing community.

My dissertation research results in novel computational approaches for highthroughput visual knowledge analysis and retrieval from large-scale databases using latest technologies in big data ecosystems. To provide a better understanding of visual reasoning, human gaze patterns are qualitatively measured spatially and temporally to model observers’ cognitive process. These gaze patterns are then indexed in a NoSQL distributed database as a visual knowledge repository, which is accessed using various unique retrieval methods developed through this dissertation work. To provide meaningful retrievals in real time, deep-learning methods for automatic annotation of visual activities and streaming similarity comparisons are developed under a gaze-streaming framework using Apache Spark.

This research has several potential applications that offer a broader impact among the scientific community and in the practical world. First, the proposed framework can be adapted for different domains, such as fine arts, life sciences, etc. with minimal effort to capture human reasoning processes. Second, with its real-time visual knowledge search function, this framework can be used for training novices in the interpretation of domain images, by helping them learn experts’ reasoning processes. Third, by helping researchers to understand human visual reasoning, it may shed light on human semantics modeling. Finally, integrating reasoning process with multimedia data, future retrieval of media could embed human perceptual reasoning for database search beyond traditional content-based media retrievals.

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Enfield, Alexander. "Investigation of the high-throughput analytical performance of an FPA-FTIR imaging system." Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=95201.

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Focal plane array (FPA) FTIR imaging spectroscopy provides unprecedented levels of spatially resolvable chemical information for analysis of samples at the micrometer scale. This study evaluates the quantitative performance characteristics of the individual detector elements comprising the FPA camera, and applies them to making analytical measurements of a custom designed microfluidic multichannel transmission cell. Statistical descriptions are provided for the response distributions among the FPA's detector elements; RMS noise, peak response, and linear regression parameters. It was found that individual detector elements of the FPA allowed for accurate milli-absorbance measurements, however the variability was large when contrasting detector elements due to FPA detector non-uniformity issues. When applied to the microfluidic multichannel sampling system designed for the monitoring of four fluid streams, it was found that the detector elements covering the fluid stream could be averaged to generate a very repeatable response between streams – thus allowing for milli-absorbance measurements of 4 samples simultaneously with the current design.
L'imagerie par spectroscopie IRTF dans la matrice plane focale (MPF) offre des niveaux de résolution spatiale sans précédent des informations chimique dans le domaine spatial pour une analyse des échantillons à l'échelle du micromètre. L'étude actuelle examine l'ensemble des applications de la spectroscopie IRTF (MPF) avec l'utilisation d'un système micro-fluidique multicanaux de transmission de cellules conçut sur mesure comme une approche potentielle d'une analyse quantitative des échantillons liquides à haut débit. Des descriptions statistiques sont fournies selon la répartition des réponses parmi ces éléments individuels du détecteur. La réponse des éléments individuels du détecteur dans la MPF a été démontrée comme étant reproductible dans des unités de milli absorbance et ainsi, la plus importante variabilité de réponse à travers l'ensemble est due aux problèmes de non conformité associés à la MPF. La moyenne des réponses des éléments du détecteur sur lesquels les résultats de chaque canal est imagées dans de bonne reproductibilité inter-canal et ainsi compense de manière satisfaisante la non-uniformité des pixels. Les expériences qui prouvent ce concept impliquant des mesures analytiques sur quatre échantillons visualisés simultanément avec la conception actuel des cellules sont présentées.
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De, Meutter Joëlle. "Infrared imaging of protein microarrays for high throughput, label-free protein structure evaluation." Doctoral thesis, Universite Libre de Bruxelles, 2021. https://dipot.ulb.ac.be/dspace/bitstream/2013/326640/4/Thesis.pdf.

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In the field of protein research in general and the pharmaceutical industry in particular, it is now necessary to perform measurements of the secondary structure of proteins on many samples simultaneously, for instance to screen for molecules that stabilize proteins or to evaluate the action of multiple environmental conditions. In this context, we have proposed a new approach to evaluate the secondary structure of proteins on a very large scale (approximately 2000 to 4000 samples / cm2), by combining infrared imaging and 2D printing of protein microarrays. In view of the large amount of data, in a first step, methods for automating the extraction of spectra of interest from microarray infrared images and for automating the processing of the spectra were developed. Since the estimation of the secondary structure from infrared spectra is based on the construction of prediction models by chemometric methods, a relevant set of proteins for calibration was mandatory. A protein bank consisting of 92 commercially available proteins, the structure of which was well characterized by X-ray crystallography, was established for this purpose. After the development of predictive models for secondary structure determination and the validation of the protein microarray approach, we tried to optimize the models to improve the secondary structure prediction by different approaches as secondary structure definition, partial deuteration or subtraction of side chain contribution to the spectra. On the other hand, dealing with non-native structures not present in the reference protein library was a challenge. We took the opportunity to analyze the structural modifications of a subset of our protein library subjected to moderate denaturation conditions. Multivariate curve resolution-alternating least squares (MCR-ALS) was used to model a new spectral component appearing in the protein set subjected to denaturing conditions, which could represent a potential spectroscopic marker of aggregation and could allow a semi-quantitative evaluation of the aggregation. While the assessment of secondary structure was well established in the first part of this work, tertiary structure and stability are also critical. Hydrogen / deuterium exchange (HDX) is a potential approach for studying the structure and dynamics of proteins. In the last part of this work, we built a device which allowed to follow the HDX exchange kinetics simultaneously on the entire microarray. In conclusion, protein microarray FTIR imaging opens the door to high throughput analysis of protein secondary structure without any labelling and would allow better understanding of three-dimensional structure and dynamics of proteins through recording HDX curves.
Dans le domaine de la recherche sur les protéines et de l'industrie pharmaceutique, il s’avère désormais nécessaire d'effectuer des mesures de la structure secondaire des protéines sur de nombreux échantillons simultanément, de cribler des molécules qui stabilisent les protéines, ou d'évaluer l'action de multiples conditions environnementales. Dans ce contexte, nous avons proposé une nouvelle approche pour évaluer la structure secondaire des protéines à très grande échelle (environ 2 000 à 4 000 échantillons / cm2), en associant l'imagerie infrarouge et l'impression 2D de damiers de protéines. Dans un premier temps, des méthodes d'automatisation de l'extraction des spectres d'intérêt à partir des images infrarouges des damiers et d'automatisation des spectres ont été développées. L'estimation de la structure secondaire à partir des spectres infrarouges étant basée sur la construction de modèles de prédiction à partir de méthodes chimiométriques, un ensemble pertinent de protéines pour l'étape de calibration était obligatoire. Une banque de protéines constituée de 92 protéines disponibles dans le commerce, dont la structure était bien caractérisée par cristallographie aux rayons X, a été constituée dans ce but. Après élaboration des modèles prédictifs de la structure secondaire et la validation de l'approche des damiers de protéines, nous avons tenté d'optimiser les modèles pour améliorer les prédictions de structure secondaire par différentes approches. D'autre part, traiter des protéines présentant une structure jamais rencontrée dans les structures natives de notre bibliothèque de protéines de référence constituait un défi. Nous avons saisi l'opportunité d'analyser les modifications structurales d'un sous-ensemble de notre bibliothèque de protéines, caractérisé par un contenu structurel secondaire très différent en le soumettant à des conditions de dénaturation modérées La méthode de résolution de courbes multivariées des moindres carrés alternés (MCR-ALS) a été utilisée pour modéliser une nouvelle composante spectrale apparaissant dans l'ensemble protéique soumis à des conditions dénaturantes, et a permis de révéler un marqueur spectroscopique potentiel d'agrégation protéique permettant une évaluation semi-quantitative de son contenu. Alors que l’évaluation de la structure secondaire a été bien établie dans la première partie de ce travail, la structure tertiaire et la stabilité sont également critiques. L'échange hydrogène / deutérium (HDX) est une approche potentielle pour l’étude de la structure et de la dynamique des protéines. Dans la dernière partie de ce travail, nous avons construit un dispositif qui a permis de suivre la cinétique d’échange HDX simultanément sur l'ensemble d’un damier. En conclusion, l'imagerie FTIR de damiers de protéines ouvre la porte à une analyse à haut débit de la structure secondaire des protéines et permettrait de mieux comprendre la structure et la dynamique tridimensionnelles grâce à l'enregistrement des courbes HDX.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
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Mathew, Mark. "High throughput imaging for anthelmintic discovery and Caenorhabditis elegans genetic tools for target elucidation." Thesis, University of British Columbia, 2015. http://hdl.handle.net/2429/56407.

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Nearly three billion humans worldwide have helminth infections, which accounts for a global disease burden of 5.2 million disability-adjusted life years. Parasitic nematodes also have a great affect on agriculture, annually destroying 12.3% of global food crops and accounting for an annual loss of approximately $10 billion (USD) worldwide in the sheep and cattle industry. There is widespread resistance to all classes of anthelmintic drugs. The last drug to enter human clinical trials was 35 years ago. There is a great need for new anthelmintics and this concern has been strongly voiced by the World Health Organization and Gates Foundation. Anthelmintics are considered rare, which is why large chemical libraries are a necessity for anthelmintic discovery. I adapted my Caenorhabditis elegans high-throughput technique WormScan to overcome the bottleneck of whole organism screening for anthelmintic discovery. WormScan was used to screen a library of approximately 26,000 molecules. Hits were tested against diverse organisms to identify nematode specific compounds. I took into account preexisting drug resistance of the established anthelmintics. For every class of anthelmintics there is a corresponding C. elegans resistant strain. Screening the hits against these known resistant strains allowed me to determine if any of the compounds target a novel or established anthelmintic pathways. A forward genetic screen and C. elegans genetic tools were employed to identify the mechanism of action of the candidate D19. Molecular modelling was undertaken to elucidate the resistance mechanism and phylogenetic specificity of the D19. I undertook a structure activity relationship to identify structural moieties of D19 activity. The high throughput screen identified 14 new potential anthelmintics, 5 of which had nematode specificity, which indicates low toxic side effects in humans and limited environmental toxicity. Forward genetic screening and molecular modelling identified D19 to be a worm specific mitochondrial complex II inhibitor. The Structure Activity Relationship demonstrated the chemical features needed for D19 activity. C. elegans was used as a surrogate of parasitic nematodes for whole organism anthelmintic discovery. This thesis is a starting point to replenish the pipeline of potential nematicides. Future studies should focus on progressing these hits to a lead status.
Pharmaceutical Sciences, Faculty of
Graduate
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Wong, Tsz-wai Terence, and 黃子維. "Optical time-stretch microscopy: a new tool for ultrafast and high-throughput cell imaging." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B5066234X.

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The exponential expansion in the field of biophotonics over the past half-century has been leading to ubiquitous basic science investigations, ranging from single cell to brain networking analysis. There is also one biophotonics technology used in clinic, which is optical coherence tomography, mostly for high-speed and high-resolution endoscopy. To keep up such momentum, new biophotonics technologies should be aiming at improving either the spatial resolution or temporal resolution of optical imaging. To this end, this thesis will address a new imaging technique which has an ultra-high temporal resolution. The applications and its cost-effective implementations will also be encompassed. In the first part, I will introduce an entirely new optical imaging modality coined as optical time-stretch microscopy. This technology allows ultra-fast real-time imaging capability with an unprecedented line-scan rate (~10 million frames per second). This ultrafast microscope is renowned as the world’s fastest camera. However, this imaging system is previously not specially designed for biophotonics applications. Through the endeavors of our group, we are able to demonstrate this optical time-stretch microscopy for biomedical applications with less biomolecules absorption and higher diffraction limited resolution (<2 μm). This ultrafast imaging technique is particularly useful for high-throughput and high-accuracy cells/drugs screening applications, such as imaging flow cytometry and emulsion encapsulated drugs imaging. In the second part, two cost-effective approaches for implementing optical time-stretch confocal microscopy are discussed in details. We experimentally demonstrate that even if we employ the two cost-effective approaches simultaneously, the images share comparable image quality to that of captured by costly specialty 1μm fiber and high-speed ( >16 GHz bandwidth) digitizer. In other words, the cost is drastically reduced while we can preserve similar image quality. At the end, I will be wrapping up my thesis by concluding all my work done and forecasting the future challenges concerning the development of optical time-stretch microscopy. In particular, three different research directions are discussed.
published_or_final_version
Electrical and Electronic Engineering
Master
Master of Philosophy
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Chung, Kwanghun. "Automated and integrated microsystems for highthroughput and high-resolution imaging, sorting, and laser ablation of C. elegans." Diss., Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/37163.

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The objective of this research is to develop automated and integrated microsystems for high-resolution imaging and high-throughput phenotyping / laser ablation of C. elegans. These microsystems take advantage of microfluidic technology for precisely handling animals and computer-aid automation for high-throughput processing. We demonstrated automated and high-throughput imaging / sorting and laser ablation of C. elegans. This thesis work is divided into four parts: development of a microsystem for imaging and sorting, development of a microsystem for laser cell ablation, development of a novel temperature measurement method, and development of pressure measurement method in microchannels. First, a microsystem was developed for high-throughput microscopy at high resolution and sorting. The microfluidic chip integrates novel microfluidic components to trap, position, immobilize, and sort/release animals. To characterize device operation and aid design of the device numerical models were developed. The experimental results demonstrate that the device operates robustly in a completely automatable manner. Additionally, a sophisticated control algorithm developed by Matthew Crane (Dr. Hang Lu¡¯s lab) automates the entire process of image acquisition, analysis, and sorting, which allows the system to operate without human intervention. This microsystem sorted worms based on their fluorescent expression pattern with over 95% accuracy per round at a rate of several hundred worms per hour. Secondly, the technologies developed for the imaging/sorting system were adapted and further improved to develop a microsystem for high-throughput cell laser ablation of C. elegans. The multiplex ablation module combined with the embryo trap module enables robust manipulation of embryos/L1-stage C. elegans. In addition, software for image processing and automation was developed to allow high-throughput cell ablations. This system performed ablation of a large number of animals and demonstrated accurate ablation by showing behavioral defects of the ablated worms in a chemotaxis avoidance assay. Thirdly, to aid future development of the microdevices, a novel in situ method for three-dimensionally resolved temperature measurement in microchannels was developed. This method uses video-microscopy in combination with image analysis software (developed by Jaekyu Cho in Dr. Victor Breedveld¡¯s group) to measure Brownian diffusion of nanoparticles that is correlated to temperature. This method offers superior reproducibility and reduced systematic errors. In addition, we demonstrated that this method can be used to measure spatial temperature variations in three dimensions in situ. Lastly, a method for pressure measurement in microdevices was also developed through collaboration with Hyewon Lee (Dr. Hang Lu¡¯s lab) to aid further device optimization. These micro pressure-sensors are composed of two flow layers with a polydimethylsiloxane (PDMS) membrane in between. The membrane deforms as a function of pressure and its deformation is quantified by a simple image-based method. These sensors offer high-precision pressure measurement in broad sensing ranges. In addition, a pressure transduction scheme combined with imaging-based method enables multiplex pressure measurement for simultaneously detecting pressures in multiple locations in a microsystem. Overall, the technologies developed in this thesis will establish a solid basis for continuous improvement of the microsystems for multi-cellular model organisms. This high-throughput technology will facilitate a broad range of biological and medical research.
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Robertson, Stuart. "The characterisation of the high throughput imaging Echelle spectrograph and investigations of hydrogen Balmer β emission over Svalbard." Thesis, University of Southampton, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433955.

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Books on the topic "High throughput imaging"

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A, Ravishankar Rao, and Cecchi Guillermo A, eds. High-throughput image reconstruction and analysis. Norwood, MA: Artech House, 2009.

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Bhunia, Arun K., Moon S. Kim, and Chris R. Taitt. High Throughput Screening for Food Safety Assessment: Biosensor Technologies, Hyperspectral Imaging and Practical Applications. Elsevier Science & Technology, 2014.

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Bhunia, A. K., M. S. Kim, and C. R. Taitt. High Throughput Screening for Food Safety Assessment: Biosensor Technologies, Hyperspectral Imaging and Practical Applications. Elsevier Science & Technology, 2014.

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Bhunia, Arun K., Moon S. Kim, and Chris R. Taitt. High Throughput Screening for Food Safety Assessment: Biosensor Technologies, Hyperspectral Imaging and Practical Applications. Woodhead Publishing, 2016.

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Clebone, Anna, Joshua H. Finkle, Barbara K. Burian, Keith J. Ruskin, and Barbara K. Burian, eds. Ultrasound Guided Procedures and Radiologic Imaging for Pediatric Anesthesiologists. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190081416.001.0001.

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Ultrasound Guided Procedures and Radiologic Imaging for Pediatric Anesthesiologists is intended as a ready resource for both experts and novices. It will be useful to those with extensive training and experience as well as beginners and those with distant experience or training. A wealth of knowledge in the human factors of procedure design and use has been applied throughout to ensure that desired information can be easily located, that steps are clearly identified and comprehensible, and that additional information of high relevance to procedure completion is co-located and salient. This book begins with the basics but quickly progresses to advanced skill sets. It is divided into four parts. Part I starts with a primer on ultrasound machine functionality as well as procedural chapters on lung ultrasound to detect a mainstem intubation or pneumothorax and gastric ultrasound to assess gastric contents in incompletely fasted patients. Part II covers ultrasound guided peripheral intravenous line placement through the incremental advancement method, ultrasound guided arterial line placement, and ultrasound guided central line placement. Part III details several ultrasound guided regional anesthesia techniques. Part IV covers radiology of the pediatric airway and mediastinum, lungs, gastrointestinal, genitourinary, musculoskeletal, and neurologic systems.
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Bergoffen, Debra. The Question of the Subject and the Matter of Violence. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190275594.003.0008.

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Negotiating the distance between Simone de Beauvoir and Luce Irigaray reveals that, despite their diverse starting points and philosophical commitments, they arrive at similar conclusions regarding the issue of violence against woman. Beauvoir’s existential–phenomenological account of the embodied vicissitudes of freedom and Irigaray’s psychoanalytic account of the bodied drives that structure human symbolic existence reveal that so long as women are signified as woman, the second sex (Beauvoir) and the power of masculine symbolic to silence all other articulations the human endures (Irigaray), men can and will imagine they are immune from the vulnerabilities of the human condition. Understanding the abuse of women throughout the ages and across the globe marks it as a symptom of the flight from vulnerability, identifies the high stakes of this flight, and directs us to develop strategies of resistance that, by resignifying the meaning of vulnerability, gets at the roots of the violence.
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Dickason, Kathryn. Ringleaders of Redemption. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780197527276.001.0001.

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In traditional thought and theology, Christianity tends to oppose dance. Conventional scholarship traces this controversy back to the Middle Ages. Throughout the medieval era, the Latin Church denounced and prohibited dancing in religious and secular realms, often aligning it with demonic intervention, lust, pride, and sacrilege. Historical sources, however, suggest that medieval dance was a complex and ambivalent phenomenon. During the High and Late Middle Ages, Western theologians, liturgists, and mystics not only tolerated dance, they transformed it into a dynamic component of religious thought and practice. This book investigates how dance became a legitimate form of devotion in Christian culture. Sacred dance functioned to gloss scripture, frame spiritual experience, and imagine the afterlife. Invoking numerous manuscript, primary, and visual sources (biblical commentaries, sermons, saints’ lives, ecclesiastical statutes, mystical treatises, vernacular literature, and iconography), this book highlights how medieval dance helped shape religious identity, social stratification, and human intention. Moreover, this book shows the political dimension of dance, which worked in the service of Christendom, conversion, and social cohesion. In sum, Ringleaders of Redemption reveals a long tradition of sacred dance in Christianity, one that the professionalization and secularization of Renaissance dance obscured, and one that the Reformation silenced and suppressed.
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Torgerson,, Paul R., C. N. L. Macpherson, and D. A. Vuitton. Cystic echinococcosis. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0060.

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Cystic echinococcosis (CE)\cystic hydatid disease is one of the most widespread and important global helminth zoonoses. The parasite Echinococcus granulosus is maintained in a wide spectrum of intermediate hosts, including sheep, goats, camels, cattle, pigs and equines. A number of wild intermediate hosts occur, including cervids in the northern part of the North American continent and Eurasia, marsupials in Australia and wild herbivores in East and southern Africa. The application of a range of molecular techniques to the characterization of the parasite has confirmed the existence of mostly host-adapted strains and genotypes of the parasite and several new species have been proposed. The ubiquitous domestic dog serves as the most important definitive host for the transmission of the parasite throughout its wide geographical range.A wide range of diagnostic techniques, including necropsy, arecoline purgation, coproantigen ELISA and DNA based tests are available for detecting E. granulosus infection in the definitive host. In intermediate animal hosts, diagnosis at post mortem still remains the most reliable option. In humans, imaging techniques including ultrasound, nuclear magnetic resonance (NMR) or computer aided tomography (CAT-scan provide not only a method of diagnosis but also reveal important clinical information on the location, condition, number and size of the hydatid cysts in man. Of these ultrasound is the most widely used diagnostic technique and is the only imaging technique for screening of populations in rural areas, where the disease is most common. A classification system has been developed which can be used to assess the likely development of a cyst and hence guide the clinician in treatment options for the patient. Treatment relies on surgery and/or percutaneous interventions, especially ‘Puncture, Aspiration, Injection, Re-aspiration’ (PAIR) and/or antiparasitic treatment with albendazole (and alternatively mebendazole).CE is largely a preventable disease. Successful elimination programmes have focused on frequent periodic treatments of dogs with anthelmintics and the control of slaughter of domestic livestock. In many regions elimination or even control remains a problem as the parasite is endemic over vast areas of low income countries where there may be limited resources for control. In some areas, such as former communist administered countries, the parasite is resurgent. New tools are becoming available to control the parasite, including a highly effective vaccine in sheep which prevents the infection in sheep and breaks the transmission cycle. In addition cost effective methods are being developed which may be appropriate in low income countries where financial resources are not available for intensive control programmes that have been successful in high income countries.
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Book chapters on the topic "High throughput imaging"

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Lasko, Steven S., Reed J. Hendershot, Yu Fu, Mark-Florian Fellmann, Gudbjorg Oskarsdottir, Christopher M. Snively, and Jochen Lauterbach. "Spectroscopic Imaging in the Mid-Infrared Applied to High-Throughput Studies of Supported Catalyst Libraries." In High-Throughput Analysis, 77–91. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-8989-5_5.

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Montero Llopis, Paula, Ryan Stephansky, and Xindan Wang. "High-Throughput Imaging of Bacillus subtilis." In Methods in Molecular Biology, 277–92. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2221-6_19.

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Pan, Liang. "Plasmonic Lenses for High-Throughput Nanolithography." In Plasmonics and Super-Resolution Imaging, 333–59. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2017. http://dx.doi.org/10.4324/9781315206530-11.

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Jokela, Tiina A., Michael E. Todhunter, and Mark A. LaBarge. "High-Throughput Microenvironment Microarray (MEMA) High-Resolution Imaging." In Methods in Molecular Biology, 47–64. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1811-0_4.

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Gradl, Gabriele, Chris Hinnah, Achim Kirsch, Jürgen Müller, Dana Nojima, and Julian Wölcke. "High-Throughput/High-Content Automated Image Acquisition and Analysis." In Imaging Cellular and Molecular Biological Functions, 385–405. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71331-9_14.

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Iyer-Pascuzzi, Anjali S., Paul R. Zurek, and Philip N. Benfey. "High-Throughput, Noninvasive Imaging of Root Systems." In Methods in Molecular Biology, 177–87. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-221-6_11.

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Beck, Martina, Ji Zhou, Christine Faulkner, and Silke Robatzek. "High-Throughput Imaging of Plant Immune Responses." In Methods in Molecular Biology, 67–80. Totowa, NJ: Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-986-4_5.

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Zhou, Jing, Chin Nee Vong, and Jianfeng Zhou. "Imaging Technology for High-Throughput Plant Phenotyping." In Sensing, Data Managing, and Control Technologies for Agricultural Systems, 75–99. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-03834-1_4.

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Herpers, Bram, and Bob van de Water. "High Content Imaging-Based Screening for Cellular Toxicity Pathways." In High-Throughput Screening Methods in Toxicity Testing, 143–57. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118538203.ch7.

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Williams, Dominic, Matt Aitkenhead, Alison J. Karley, Julie Graham, and Hamlyn G. Jones. "Use of Imaging Technologies for High Throughput Phenotyping." In Raspberry, 145–58. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-99031-6_9.

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Conference papers on the topic "High throughput imaging"

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Pisani, M., P. Bianco, and M. Zucco. "High throughput, compact imaging spectrometer." In International Conference on Space Optics 2010, edited by Naoto Kadowaki. SPIE, 2017. http://dx.doi.org/10.1117/12.2309244.

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Choi, Heejin, Jaehun Cho, Taeyun Ku, and Kwanghun Chung. "High Throughput Multiscale Brain Imaging." In Bio-Optics: Design and Application. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/boda.2017.jtu4a.12.

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Wu, Jiahua, Junyu Dong, and Huiyu Zhou. "Image quantification of high-throughput tissue microarray." In Medical Imaging, edited by Armando Manduca and Amir A. Amini. SPIE, 2006. http://dx.doi.org/10.1117/12.653564.

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Scarcelli, Giuliano. "Towards high-throughput Brillouin microscopy." In High-Speed Biomedical Imaging and Spectroscopy VII, edited by Keisuke Goda and Kevin K. Tsia. SPIE, 2022. http://dx.doi.org/10.1117/12.2610987.

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So, Peter T. C. "High Throughput Tissue Imaging and Bioinformatics." In Biomedical Optics. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/biomed.2008.btua1.

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Tian, Lei. "Computational high-throughput microscopy using coded illumination." In Mathematics in Imaging. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/math.2017.mw3c.4.

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Haefner, David P., Stephen D. Burks, and Joshua M. Doe. "High throughput thermal camera characterization." In Infrared Imaging Systems: Design, Analysis, Modeling, and Testing XXXII, edited by Gerald C. Holst and David P. Haefner. SPIE, 2021. http://dx.doi.org/10.1117/12.2586515.

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Geerts, Stan J. C., Dion Cornelissen, and Peter H. N. de With. "Embedded image enhancement for high-throughput cameras." In IS&T/SPIE Electronic Imaging, edited by Robert P. Loce and Eli Saber. SPIE, 2014. http://dx.doi.org/10.1117/12.2036966.

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Schonbrun, Ethan. "Diffractive Optics for High-throughput Screening." In Applied Industrial Optics: Spectroscopy, Imaging and Metrology. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/aio.2011.aituc3.

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Mahjoubfar, A., C. Chen, K. R. Niazi, S. Rabizadeh, and B. Jalali. "Label-free high-throughput imaging flow cytometry." In SPIE LASE, edited by Alexander Heisterkamp, Peter R. Herman, Michel Meunier, and Stefan Nolte. SPIE, 2014. http://dx.doi.org/10.1117/12.2040881.

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Reports on the topic "High throughput imaging"

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Sharp, Zelton D. Quantifying ER Function Using High-Throughput Imaging in Breast and Other Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada502583.

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Scanlan, E. J., M. Leybourne, D. Layton-Matthews, A. Voinot, and N. van Wagoner. Alkaline magmatism in the Selwyn Basin, Yukon: relationship to SEDEX mineralization. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328994.

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Several sedimentary exhalative (SEDEX) deposits have alkaline magmatism that is temporally and spatially associated to mineralization. This report outlines interim data from a study of potential linkages between magmatism and SEDEX mineralization in the Selwyn Basin, Yukon. This region is an ideal study site due to the close spatial and temporal relationships between SEDEX deposits and magmatism, particularly in the MacMillan Pass, where volcanic rocks have been drilled with mineralization at the Boundary deposit. Alkaline volcanic samples were analysed from the Anvil District, MacMillan Pass, Keno-Mayo and the Misty Creek Embayment in the Selwyn Basin to characterise volcanism and examine the relationship to mineralization. Textural and field relationships indicate a volatile-rich explosive eruptive volcanic system in the MacMillan Pass region in comparison to the Anvil District, which is typically effusive in nature. High proportions of calcite and ankerite in comparison to other minerals are present in the MacMillan system. Cathodoluminescence imaging reveals zoning and carbonate that displays different luminescent colours within the same sample, likely indicating multiple generations of carbonate precipitation. Barium contents are enriched in volcanic rocks throughout the Selwyn Basin, which is predominately hosted by hyalophane with rare barite and barytocalcite. Thallium is positively correlated with Ba, Rb, Cs, Mo, As, Sb and the calcite-chlorite-pyrite index and is negatively correlated with Cu. Anvil District samples display a trend towards depleted mid-ocean ridge mantle on a plot of Ce/Tl versus Th/Rb. Hydrothermal alteration has likely led to the removal of Tl from volcanic rocks in the region. Ongoing research involves: i) the analysis of Sr, Nd, Pb and Tl isotopes of volcanic samples; ii) differentiating magmatic from hydrothermal carbonate using O, C and Sr isotopes; iii) examining sources of Ba in the Selwyn Basin; iv) and constraining age relationships through U-Th-Pb geochronology.
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