Дисертації з теми "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.
Повний текст джерелаCabello, Velasco J. "High throughput digital beta autoradiography imaging." Thesis, University of Surrey, 2009. http://epubs.surrey.ac.uk/844626/.
Повний текст джерелаRock, Reza M. "An Imaging Ammeter for High Throughput Electrochemical Research." Research Showcase @ CMU, 2013. http://repository.cmu.edu/dissertations/235.
Повний текст джерелаCao, 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.
Повний текст джерелаVisual 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.
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.
Повний текст джерелаL'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.
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.
Повний текст джерелаDans 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
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.
Повний текст джерелаPharmaceutical Sciences, Faculty of
Graduate
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.
Повний текст джерелаpublished_or_final_version
Electrical and Electronic Engineering
Master
Master of Philosophy
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.
Повний текст джерелаRobertson, 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.
Повний текст джерелаJoshi, Pranav. "Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity." Cleveland State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=csu155965254496159.
Повний текст джерелаChen, Huiyi. "System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing." Thesis, Harvard University, 2011. http://dissertations.umi.com/gsas.harvard:10044.
Повний текст джерелаHelfrich, Stefan Verfasser], Wolfgang [Akademischer Betreuer] Wiechert, and Björn [Akademischer Betreuer] [Usadel. "High-throughput live-cell imaging for investigations of cellular heterogeneity in Corynebacterium glutamicum / Stefan Helfrich ; Wolfgang Wiechert, Björn Usadel." Aachen : Universitätsbibliothek der RWTH Aachen, 2016. http://d-nb.info/1129875989/34.
Повний текст джерелаHelfrich, Stefan [Verfasser], Wolfgang Akademischer Betreuer] Wiechert, and Björn [Akademischer Betreuer] [Usadel. "High-throughput live-cell imaging for investigations of cellular heterogeneity in Corynebacterium glutamicum / Stefan Helfrich ; Wolfgang Wiechert, Björn Usadel." Aachen : Universitätsbibliothek der RWTH Aachen, 2016. http://d-nb.info/1129875989/34.
Повний текст джерелаLu, Yi-Ju [Verfasser], and Jane [Akademischer Betreuer] Parker. "Live-cell imaging reveals subcellular localization of plant membrane compartments during oomycete infections and quantitative high-throughput imaging identifies endocytic trafficking mutants / Yi-Ju Lu. Gutachter: Jane Parker." Köln : Universitäts- und Stadtbibliothek Köln, 2012. http://d-nb.info/1038225981/34.
Повний текст джерелаEismann, Björn Benjamin [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Comparative assessment of induced abnormal mitotic events by high-throughput light sheet imaging and image analysis / Björn Benjamin Eismann ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2019. http://d-nb.info/1197692762/34.
Повний текст джерелаEismann, Björn [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Comparative assessment of induced abnormal mitotic events by high-throughput light sheet imaging and image analysis / Björn Benjamin Eismann ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2019. http://d-nb.info/1197692762/34.
Повний текст джерелаFlottmann, Benjamin [Verfasser], and Andriy [Akademischer Betreuer] Mokhir. "Implementation of Multi-Color Super-Resolution Microscopy into a High-Throughput Platform for Quantitative Imaging of Cellular Structures / Benjamin Flottmann ; Betreuer: Andriy Mokhir." Heidelberg : Universitätsbibliothek Heidelberg, 2014. http://d-nb.info/1180032276/34.
Повний текст джерелаKloster, Michael [Verfasser], Anya [Akademischer Betreuer] Waite, Andres Salavdor [Gutachter] Rigual-Hernández, and Gastón Osvaldo [Gutachter] Almandoz. "Morphometrics of Southern Ocean diatoms using high throughput imaging and semi-automated image analysis / Michael Kloster ; Gutachter: Andres Salavdor Rigual-Hernández, Gastón Osvaldo Almandoz ; Betreuer: Anya Waite." Bremen : Staats- und Universitätsbibliothek Bremen, 2018. http://d-nb.info/1161844414/34.
Повний текст джерелаLindström, Sara. "Microwell devices for single-cell analyses." Doctoral thesis, KTH, Nanobioteknologi, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-11665.
Повний текст джерелаQC 20100728
Woods, Adam Xavier. "Exploring Combinatorial Libraries for Material Screening Techniques via Additive Manufacturing: Design, Fabrication, & Applications." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1594772957272505.
Повний текст джерелаPillet, Flavien. "Développement d'un outil d'analyse d'interactions moléculaires basé sur la résonance plasmonique de surface (SPRi)." Thesis, Toulouse, INSA, 2010. http://www.theses.fr/2010ISAT0029/document.
Повний текст джерелаDuring the last decades a large number of technologies have been developed to analyze intermolecular interactions. In this context, the fluorescence biochips remain the most frequently used. Although this technology is very sensitive and multiplexed, it does not allow access to the kinetic parameters, essential to the calculation of the constants of affinity. Therefore, the research for alternative systems is essential. In this way, the Surface Plasmon Resonance imaging (SPRi) is considered as an opportunity. It is an optical detection process that can occur when a polarized light hits a prism covered by a thin metal layer. Under certain conditions free electrons at the surface of the biochip absorb incident light photons and convert them into surface plasmon waves. Perturbations at the surface of the biochip, such as an interaction between probes immobilized on the chip and targets, induce a modification of resonance conditions which can be measured. It is a label free technology which allows intermolecular interactions in real time and gives access to the kinetics parameters. However, SPRi is limited in sensitivity and multiplexing. The objectives of my PhD were to circumvent these various limits. Thus, we validated the immobilization of DNA probes on gold surface using thiol-modified oligonucleotide probes. Deposition carried out on non-modified gold surface, does not require electrical stimulation and expensive specific robotic devices. The thiol modification of the probes was shown to be very stable at room temperature, contrary to pyrrole and diazonium probes that need to be prepared just prior to their spotting. We demonstrate that thiol-modified oligonucleotide probes spotted on a gold surface of the SPRi-prisms are very robust and reproducible. We also demonstrated that this simple chemistry is compatible with high density arrays fabrication bearing more than 1000 spots using a classical spotter. Furthermore, the modification of the prism surface with gold colloids and dendrimers allowed for DNA/DNA interactions, to reach a detection limit of 2 nM. In parallel of this work, various biological applications were carried out and validate our previous developments. A first study was to screen G-quadruplex specific ligands to inhibit telomerase activity. We demonstrated that SPRi technology is particularly well adapted to the screening of interaction of small molecules with DNA probes and is sensitive enough to permit distinction between interactions with different DNA structures. The second study was on the bacterial partition complex. We study the DNA binding requirement involved in SopB-sopC specific interactions and analysed at the nucleotide level the bases involved in the binding efficiency and essential for the partition All this PhD work improved the SPRi technology and demonstrated its great potential in biological applications
Adanja, Ivan. "Automated tracking of unmarked cells migrating in three-dimensional matrices." Doctoral thesis, Universite Libre de Bruxelles, 2012. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209703.
Повний текст джерелаThe focus in this thesis lies in two specific aspects that are important in anti-migratory drug screening: tracking cells inside an in vitro 3D environment and doing so using unmarked cells.
Doctorat en Sciences de l'ingénieur
info:eu-repo/semantics/nonPublished
Cerrato, Giulia. "Oleate : An Atypical Cellular Stress Inducer That Stalls Protein Secretion Oleate-Induced Aggregation of LC3 at the Trans-Golgi Network Is Linked to a Protein Trafficking Blockade A Genome-Wide RNA Interference Screen Disentangles the Golgi Tropism of LC3 Live Cell Imaging of LC3 Dynamics." Thesis, université Paris-Saclay, 2021. http://www.theses.fr/2021UPASL023.
Повний текст джерелаDistinct classes of fatty acids (FAs) (saturated or cis-/trans-unsaturated carbon chains) impact on cellular and organismal physiology in a different manner. Interestingly, these diverse categories have a profound (but different) effect on autophagy, the conserved intracellular degradation mechanism that maintains energy homeostasis and protects cells against stress. Oleate, the most abundant endogenous and dietary cis-unsaturated FA, has the atypical property to induce the redistribution of the LC3 protein (peculiar sign of autophagy) in a non-canonical fashion and preferentially to the Golgi apparatus. Intrigued by these observations, which might be related to the health-improving effects of cis-unsaturated FAs (and the notorious toxicity of trans-unsaturated and saturated FAs), we decided to explore the mechanisms causing the oleate-induced relocation of LC3 to the Golgi apparatus. To achieve this goal, a robotized RNA interference genome-wide screen led to the identification of multiple genes involved in the Golgi-related protein transport, as well as in the integrated stress response. Follow-up experiments revealed that oleate affected the subcellular morphology of the Golgi apparatus, correlating with a blockade of conventional (Golgi-dependent) protein secretion that caused secretory cargo to be stalled at the level of the trans-Golgi network. The inhibition of protein secretion was observed using several experimental systems, both in vitro and in vivo. Moreover, a systematic screen searching for other chemical entities that mimic the oleate-induced cellular effects led to the identification of several compounds belonging to rather different pharmacological classes. These “oleate mimetics” also shared with oleate the capacity to block conventional protein secretion, supporting the notion that this pathway of Golgi perturbation is indeed of pharmacological relevance. In conclusion, this research work shows that oleate represents a class of molecules that act on the Golgi apparatus to cause the recruitment of LC3 and to stall protein secretion
Regmi, Raju. "Light Sheet Based Microfluidic Flow Cytometry Techniques for High throughput Interrogation and High-resolution Imaging." Thesis, 2014. http://hdl.handle.net/2005/3108.
Повний текст джерелаJagannadh, Veerendra Kalyan. "Point-of-Care High-throughput Optofluidic Microscope for Quantitative Imaging Cytometry." Thesis, 2017. http://hdl.handle.net/2005/3274.
Повний текст джерелаLO, SHU-CHENG, and 駱書成. "Development of Curved Grating for Imaging Spectrometer and High-throughput Sensing." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/63708958674151411853.
Повний текст джерелаChan, Chia-Kai, and 詹家愷. "High-Throughput 64K-point FFT Processor for THz Imaging Radar System." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/5r373m.
Повний текст джерела國立交通大學
電子研究所
107
Radar technology and its developments have been important issues for decades. In recent years, related applications are becoming more and more popular such as automobile safety system and speed measurement. With the growth of semiconductor processing technology, the development of circuit design related to THz technology has gradually been noted. Imaging radar system with THz technology has many advantages so that it can be applied on security scan, because of the characteristics of THz such as penetrability and reflection on conducting material. However, there are ultra-long series in the application of wideband radar system with high sampling rate. While realizing the ultra-long FFT, it would introduce some design challenges such as high hardware complexity and large area cost. On the other hand, it needs to achieve a high throughput rate to meet the requirement of real-time processing. In this thesis, we implement a 4-parallel 64K-point FFT hardware architecture based on the 2-epoch FFT algorithm for the application of THz imaging radar system. With the proposed middle twiddle factor generator, we can reduce a large number of storages for twiddle factor coefficients, so the area of ROM is reduced. In addition, the maximum operating frequency will not be limited by the long access time of a large size ROM. We implement the 64K-point FFT architecture in TSMC 90 nm CMOS technology with high-Vt standard cell library. The maximum operating frequency of the system is 390 MHz, and the throughput rate reaches 1.57 GS/s. Its high throughput rate meets the requirement of real-time processing in our THz imaging radar system with a mechanical scan. When operating at the maximum clock rate, it consumes 0.2811 W (@0.9 V), and the total gate counts of this work are around 3974.1k.
Ramirez, Marc Stephen. "A 20-coil array system for high-throughput dynamic contrast-enhanced mouse MRI." 2011. http://hdl.handle.net/2152/20659.
Повний текст джерелаtext
Shi, Lixue. "Vibrational microscopy for super-multiplexing, vibrational sensing and high-throughput metabolic imaging." Thesis, 2020. https://doi.org/10.7916/d8-85zn-4p12.
Повний текст джерелаMace, Daniel L. "Automated Microscopy and High Throughput Image Analysis in Arabidopsis and Drosophila." Diss., 2009. http://hdl.handle.net/10161/1147.
Повний текст джерелаDevelopment of a single cell into an adult organism is accomplished through an elaborate and complex cascade of spatiotemporal gene expression. While methods exist for capturing spatiotemporal expression patterns---in situ hybridization, reporter constructs, fluorescent tags---these methods have been highly laborious, and results are frequently assessed by subjective qualitative comparisons. To address these issues, methods must be developed for automating the capture of images, as well as for the normalization and quantification of the resulting data. In this thesis, I design computational approaches for high throughput image analysis which can be grouped into three main areas. First, I develop methods for the capture of high resolution images from high throughput platforms. In addition to the informatics aspect of this problem, I also devise a novel multiscale probabilistic model that allows us to identify and segment objects in an automated fashion. Second, high resolution images must be registered and normalized to a common frame of reference for cross image comparisons. To address these issues, I implement approaches for image registration using statistical shape models and non-rigid registration. Lastly, I validate the spatial expression data obtained from microscopy images to other known spatial expression methods, and develop methods for comparing and calculating the significance between spatial expression patterns. I demonstrate these methods on two model developmental organisms: Arabidopsis and Drosophila.
Dissertation
Han, Chao. "Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening." Thesis, 2015. https://thesis.library.caltech.edu/8763/1/Han_Chao_2015_Thesis.pdf.
Повний текст джерелаWide field-of-view (FOV) microscopy is of high importance to biological research and clinical diagnosis where a high-throughput screening of samples is needed. This thesis presents the development of several novel wide FOV imaging technologies and demonstrates their capabilities in longitudinal imaging of living organisms, on the scale of viral plaques to live cells and tissues.
The ePetri Dish is a wide FOV on-chip bright-field microscope. Here we applied an ePetri platform for plaque analysis of murine norovirus 1 (MNV-1). The ePetri offers the ability to dynamically track plaques at the individual cell death event level over a wide FOV of 6 mm × 4 mm at 30 min intervals. A density-based clustering algorithm is used to analyze the spatial-temporal distribution of cell death events to identify plaques at their earliest stages. We also demonstrate the capabilities of the ePetri in viral titer count and dynamically monitoring plaque formation, growth, and the influence of antiviral drugs.
We developed another wide FOV imaging technique, the Talbot microscope, for the fluorescence imaging of live cells. The Talbot microscope takes advantage of the Talbot effect and can generate a focal spot array to scan the fluorescence samples directly on-chip. It has a resolution of 1.2 μm and a FOV of ~13 mm2. We further upgraded the Talbot microscope for the long-term time-lapse fluorescence imaging of live cell cultures, and analyzed the cells’ dynamic response to an anticancer drug.
We present two wide FOV endoscopes for tissue imaging, named the AnCam and the PanCam. The AnCam is based on the contact image sensor (CIS) technology, and can scan the whole anal canal within 10 seconds with a resolution of 89 μm, a maximum FOV of 100 mm × 120 mm, and a depth-of-field (DOF) of 0.65 mm. We also demonstrate the performance of the AnCam in whole anal canal imaging in both animal models and real patients. In addition to this, the PanCam is based on a smartphone platform integrated with a panoramic annular lens (PAL), and can capture a FOV of 18 mm × 120 mm in a single shot with a resolution of 100─140 μm. In this work we demonstrate the PanCam’s performance in imaging a stained tissue sample.
Lee, Cheng-Yu, and 李政育. "Multipoint Parallel Excitation and CCD Based Imaging System for High-throughput Fluorescence Detection of Biochip Micro-arrays." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/54853000770825209342.
Повний текст джерела"A Simple Microfluidic Device for Automated, High-Throughput Measurement of Morphology of Stored Red Blood Cells." Tulane University, 2013.
Знайти повний текст джерелаacase@tulane.edu
Palmer, William Moreau. "Clarifying assimilate transport & storage in monocot stems." Thesis, 2017. http://hdl.handle.net/1959.13/1354370.
Повний текст джерелаThis thesis is quite diverse in nature. The first section is about three dimensional imaging, the second about high throughput phenotyping and the third genetic sequencing. It is all driven towards trying to understand how sugars are stored in stems. Each section contained within has an explanation of how and why this diversity was conducted. It has coalesced into novel techniques, inventions and genetic targets that when combined will undoubtedly help drive understanding of the post phloem pathway.
Niu, Wei. "Development of imaging-based high-throughput genetic assays and genomic evaluation of yeast gene function in cell cycle progression." Thesis, 2007. http://hdl.handle.net/2152/3606.
Повний текст джерела(9224231), Dongdong Ma. "Ameliorating Environmental Effects on Hyperspectral Images for Improved Phenotyping in Greenhouse and Field Conditions." Thesis, 2020.
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