523 research outputs found

    Analysis and monitoring of single HaCaT cells using volumetric Raman mapping and machine learning

    Get PDF
    No explorer reached a pole without a map, no chef served a meal without tasting, and no surgeon implants untested devices. Higher accuracy maps, more sensitive taste buds, and more rigorous tests increase confidence in positive outcomes. Biomedical manufacturing necessitates rigour, whether developing drugs or creating bioengineered tissues [1]–[4]. By designing a dynamic environment that supports mammalian cells during experiments within a Raman spectroscope, this project provides a platform that more closely replicates in vivo conditions. The platform also adds the opportunity to automate the adaptation of the cell culture environment, alongside spectral monitoring of cells with machine learning and three-dimensional Raman mapping, called volumetric Raman mapping (VRM). Previous research highlighted key areas for refinement, like a structured approach for shading Raman maps [5], [6], and the collection of VRM [7]. Refining VRM shading and collection was the initial focus, k-means directed shading for vibrational spectroscopy map shading was developed in Chapter 3 and exploration of depth distortion and VRM calibration (Chapter 4). “Cage” scaffolds, designed using the findings from Chapter 4 were then utilised to influence cell behaviour by varying the number of cage beams to change the scaffold porosity. Altering the porosity facilitated spectroscopy investigation into previously observed changes in cell biology alteration in response to porous scaffolds [8]. VRM visualised changed single human keratinocyte (HaCaT) cell morphology, providing a complementary technique for machine learning classification. Increased technical rigour justified progression onto in-situ flow chamber for Raman spectroscopy development in Chapter 6, using a Psoriasis (dithranol-HaCaT) model on unfixed cells. K-means-directed shading and principal component analysis (PCA) revealed HaCaT cell adaptations aligning with previous publications [5] and earlier thesis sections. The k-means-directed Raman maps and PCA score plots verified the drug-supplying capacity of the flow chamber, justifying future investigation into VRM and machine learning for monitoring single cells within the flow chamber

    Design of new algorithms for gene network reconstruction applied to in silico modeling of biomedical data

    Get PDF
    Programa de Doctorado en Biotecnología, Ingeniería y Tecnología QuímicaLínea de Investigación: Ingeniería, Ciencia de Datos y BioinformáticaClave Programa: DBICódigo Línea: 111The root causes of disease are still poorly understood. The success of current therapies is limited because persistent diseases are frequently treated based on their symptoms rather than the underlying cause of the disease. Therefore, biomedical research is experiencing a technology-driven shift to data-driven holistic approaches to better characterize the molecular mechanisms causing disease. Using omics data as an input, emerging disciplines like network biology attempt to model the relationships between biomolecules. To this effect, gene co- expression networks arise as a promising tool for deciphering the relationships between genes in large transcriptomic datasets. However, because of their low specificity and high false positive rate, they demonstrate a limited capacity to retrieve the disrupted mechanisms that lead to disease onset, progression, and maintenance. Within the context of statistical modeling, we dove deeper into the reconstruction of gene co-expression networks with the specific goal of discovering disease-specific features directly from expression data. Using ensemble techniques, which combine the results of various metrics, we were able to more precisely capture biologically significant relationships between genes. We were able to find de novo potential disease-specific features with the help of prior biological knowledge and the development of new network inference techniques. Through our different approaches, we analyzed large gene sets across multiple samples and used gene expression as a surrogate marker for the inherent biological processes, reconstructing robust gene co-expression networks that are simple to explore. By mining disease-specific gene co-expression networks we come up with a useful framework for identifying new omics-phenotype associations from conditional expression datasets.In this sense, understanding diseases from the perspective of biological network perturbations will improve personalized medicine, impacting rational biomarker discovery, patient stratification and drug design, and ultimately leading to more targeted therapies.Universidad Pablo de Olavide de Sevilla. Departamento de Deporte e Informátic

    Machine Learning Approaches for Semantic Segmentation on Partly-Annotated Medical Images

    Get PDF
    Semantic segmentation of medical images plays a crucial role in assisting medical practitioners in providing accurate and swift diagnoses; nevertheless, deep neural networks require extensive labelled data to learn and generalise appropriately. This is a major issue in medical imagery because most of the datasets are not fully annotated. Training models with partly-annotated datasets generate plenty of predictions that belong to correct unannotated areas that are categorised as false positives; as a result, standard segmentation metrics and objective functions do not work correctly, affecting the overall performance of the models. In this thesis, the semantic segmentation of partly-annotated medical datasets is extensively and thoroughly studied. The general objective is to improve the segmentation results of medical images via innovative supervised and semi-supervised approaches. The main contributions of this work are the following. Firstly, a new metric, specifically designed for this kind of dataset, can provide a reliable score to partly-annotated datasets with positive expert feedback in their generated predictions by exploiting all the confusion matrix values except the false positives. Secondly, an innovative approach to generating better pseudo-labels when applying co-training with the disagreement selection strategy. This method expands the pixels in disagreement utilising the combined predictions as a guide. Thirdly, original attention mechanisms based on disagreement are designed for two cases: intra-model and inter-model. These attention modules leverage the disagreement between layers (from the same or different model instances) to enhance the overall learning process and generalisation of the models. Lastly, innovative deep supervision methods improve the segmentation results by training neural networks one subnetwork at a time following the order of the supervision branches. The methods are thoroughly evaluated on several histopathological datasets showing significant improvements

    Computational Imaging for Phase Retrieval and Biomedical Applications

    Get PDF
    In conventional imaging, optimizing hardware is prioritized to enhance image quality directly. Digital signal processing is viewed as supplementary. Computational imaging intentionally distorts images through modulation schemes in illumination or sensing. Then its reconstruction algorithms extract desired object information from raw data afterwards. Co-designing hardware and algorithms reduces demands on hardware and achieves the same or even better image quality. Algorithm design is at the heart of computational imaging, with model-based inverse problem or data-driven deep learning methods as approaches. This thesis presents research work from both perspectives, with a primary focus on the phase retrieval issue in computational microscopy and the application of deep learning techniques to address biomedical imaging challenges. The first half of the thesis begins with Fourier ptychography, which was employed to overcome chromatic aberration problems in multispectral imaging. Then, we proposed a novel computational coherent imaging modality based on Kramers-Kronig relations, aiming to replace Fourier ptychography as a non-iterative method. While this approach showed promise, it lacks certain essential characteristics of the original Fourier ptychography. To address this limitation, we introduced two additional algorithms to form a whole package scheme. Through comprehensive evaluation, we demonstrated that the combined scheme outperforms Fourier ptychography in achieving high-resolution, large field-of-view, aberration-free coherent imaging. The second half of the thesis shifts focus to deep-learning-based methods. In one project, we optimized the scanning strategy and image processing pipeline of an epifluorescence microscope to address focus issues. Additionally, we leveraged deep-learning-based object detection models to automate cell analysis tasks. In another project, we predicted the polarity status of mouse embryos from bright field images using adapted deep learning models. These findings highlight the capability of computational imaging to automate labor-intensive processes, and even outperform humans in challenging tasks.</p

    Text Mining for Pathway Curation

    Get PDF
    Biolog:innen untersuchen häufig Pathways, Netzwerke von Interaktionen zwischen Proteinen und Genen mit einer spezifischen Funktion. Neue Erkenntnisse über Pathways werden in der Regel zunächst in Publikationen veröffentlicht und dann in strukturierter Form in Lehrbüchern, Datenbanken oder mathematischen Modellen weitergegeben. Deren Kuratierung kann jedoch aufgrund der hohen Anzahl von Publikationen sehr aufwendig sein. In dieser Arbeit untersuchen wir wie Text Mining Methoden die Kuratierung unterstützen können. Wir stellen PEDL vor, ein Machine-Learning-Modell zur Extraktion von Protein-Protein-Assoziationen (PPAs) aus biomedizinischen Texten. PEDL verwendet Distant Supervision und vortrainierte Sprachmodelle, um eine höhere Genauigkeit als vergleichbare Methoden zu erreichen. Eine Evaluation durch Expert:innen bestätigt die Nützlichkeit von PEDLs für Pathway-Kurator:innen. Außerdem stellen wir PEDL+ vor, ein Kommandozeilen-Tool, mit dem auch Nicht-Expert:innen PPAs effizient extrahieren können. Drei Kurator:innen bewerten 55,6 % bis 79,6 % der von PEDL+ gefundenen PPAs als nützlich für ihre Arbeit. Die große Anzahl von PPAs, die durch Text Mining identifiziert werden, kann für Forscher:innen überwältigend sein. Um hier Abhilfe zu schaffen, stellen wir PathComplete vor, ein Modell, das nützliche Erweiterungen eines Pathways vorschlägt. Es ist die erste Pathway-Extension-Methode, die auf überwachtem maschinellen Lernen basiert. Unsere Experimente zeigen, dass PathComplete wesentlich genauer ist als existierende Methoden. Schließlich schlagen wir eine Methode vor, um Pathways mit komplexen Ereignisstrukturen zu erweitern. Hier übertrifft unsere neue Methode zur konditionalen Graphenmodifikation die derzeit beste Methode um 13-24% Genauigkeit in drei Benchmarks. Insgesamt zeigen unsere Ergebnisse, dass Deep Learning basierte Informationsextraktion eine vielversprechende Grundlage für die Unterstützung von Pathway-Kurator:innen ist.Biological knowledge often involves understanding the interactions between molecules, such as proteins and genes, that form functional networks called pathways. New knowledge about pathways is typically communicated through publications and later condensed into structured formats such as textbooks, pathway databases or mathematical models. However, curating updated pathway models can be labour-intensive due to the growing volume of publications. This thesis investigates text mining methods to support pathway curation. We present PEDL (Protein-Protein-Association Extraction with Deep Language Models), a machine learning model designed to extract protein-protein associations (PPAs) from biomedical text. PEDL uses distant supervision and pre-trained language models to achieve higher accuracy than the state of the art. An expert evaluation confirms its usefulness for pathway curators. We also present PEDL+, a command-line tool that allows non-expert users to efficiently extract PPAs. When applied to pathway curation tasks, 55.6% to 79.6% of PEDL+ extractions were found useful by curators. The large number of PPAs identified by text mining can be overwhelming for researchers. To help, we present PathComplete, a model that suggests potential extensions to a pathway. It is the first method based on supervised machine learning for this task, using transfer learning from pathway databases. Our evaluations show that PathComplete significantly outperforms existing methods. Finally, we generalise pathway extension from PPAs to more realistic complex events. Here, our novel method for conditional graph modification outperforms the current best by 13-24% accuracy on three benchmarks. We also present a new dataset for event-based pathway extension. Overall, our results show that deep learning-based information extraction is a promising basis for supporting pathway curators
    corecore