A micro-XRT image analysis and machine learning methodology for the characterisation of multi-particulate capsule formulations.
Ontology highlight
ABSTRACT:
SUBMITTER: Doerr FJS
PROVIDER: S-EPMC6997304 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:BackgroundAbattoir detected pathologies are of crucial importance to both pig production and food safety. Usually, more than one pathology coexist in a pig herd although it often remains unknown how these different pathologies interrelate to each other. Identification of the associations between different pathologies may facilitate an improved understanding of their underlying biological linkage, and support the veterinarians in encouraging control strategies aimed at reducing the prevalence of not just one, but two or more conditions simultaneously.ResultsMulti-dimensional machine learning methodology was used to identify associations between ten typical pathologies in 6485 batches of slaughtered finishing pigs, assisting the comprehension of their biological association. Pathologies potentially associated with septicaemia (e.g. pericarditis, peritonitis) appear interrelated, suggesting on-going bacterial challenges by pathogens such as Haemophilus parasuis and Streptococcus suis. Furthermore, hepatic scarring appears interrelated with both milk spot livers (Ascaris suum) and bacteria-related pathologies, suggesting a potential multi-pathogen nature for this pathology.ConclusionsThe application of novel multi-dimensional machine learning methodology provided new insights into how typical pig pathologies are potentially interrelated at batch level. The methodology presented is a powerful exploratory tool to generate hypotheses, applicable to a wide range of studies in veterinary research.
| S-EPMC3483212 | biostudies-literature
Project description:Abundant accumulation of digital histopathological images has led to the increased demand for their analysis, such as computer-aided diagnosis using machine learning techniques. However, digital pathological images and related tasks have some issues to be considered. In this mini-review, we introduce the application of digital pathological image analysis using machine learning algorithms, address some problems specific to such analysis, and propose possible solutions.
| S-EPMC6158771 | biostudies-other
Project description:Addressing the challenges in effectively extracting multi-scale features and preserving pose information during hyperspectral image (HSI) classification, a Multi-Scale Depthwise Separable Capsule Network (MDSC-Net) is proposed in this article for HSI classification. Initially, hierarchical features are extracted by MDSC-Net through the employment of parallel multi-scale convolutional kernels, while computational complexity is reduced via depthwise separable convolutions, thus reducing the overall computational load and achieving efficient feature extraction. Subsequently, to enhance the translational invariance of features and reduce the loss of pose information, features of various scales are processed in parallel by independent capsule networks, with improvements in max pooling achieved through dynamic routing. Lastly, features of different scales are concatenated and integrated through the concatenate operation, thereby facilitating precise analysis of multi-level information in the hyperspectral image classification process. Experimental comparisons demonstrate that MDSC-Net achieves average accuracies of 94%, 98%, and 99% on the Kennedy Space Center, University of Pavia, and Salinas datasets, respectively, indicating a significant performance advantage over recent HSI classification models and validating the effectiveness of the proposed model.
| S-EPMC11357079 | biostudies-literature
Project description:The differentiation of induced pluripotent stem cells (iPSCs) into diverse functional cell types provides a promising solution to support drug discovery, disease modeling, and regenerative medicine. However, functional cell differentiation is currently limited by the substantial line-to-line and batch-to-batch variability, which severely impede the progress of scientific research and the manufacturing of cell products. For instance, iPSC-to-cardiomyocyte (CM) differentiation is vulnerable with great sensitivity to inappropriate doses of CHIR99021 (CHIR) that are applied in the initial stage of mesoderm differentiation. Here, by harnessing live-cell bright-field imaging and machine learning (ML), we realize real-time cell recognition in the entire differentiation process, e.g., CMs, cardiac progenitor cells (CPCs), iPSC clones, and even misdifferentiated cells. This enables non-invasive prediction of differentiation efficiency, purification of ML-recognized CMs and CPCs for reducing cell contamination, early assessment of the CHIR dose for correcting the misdifferentiation trajectory, and evaluation of initial iPSC colonies for controlling the start point of differentiation, all of which provide a more invulnerable differentiation method with resistance to variability. Moreover, with the established ML models as a readout for the chemical screen, we identify a CDK8 inhibitor to further improve the cell resistance to the overdose of CHIR. Together, this study indicates that artificial intelligence is able to guide and iteratively optimize iPSC differentiation to achieve consistently high efficiency across cell lines and batches, providing a better understanding and rational modulation of the differentiation process for functional cell manufacturing in biomedical applications. With the assistance of RNA sequencing, we transcriptomically characterize the image-recognized CPCs (IR-CPCs), the cells treated with different CHIR doses at stage I, iPSC-CM treated with or without BI-1347, and cells treated with or without BI-1347 at stage I.
2023-04-01 | GSE226159 | GEO
Project description:The correct operation of the backwashing process in sand filters used in micro irrigation determines directly the effectiveness of the subsequent filtration processes, and consequently the micro irrigation systems maintenance. As backwashing involves the filter bed expansion, the current sand filter design makes it impossible to measure the process. In this sense, this work aims to present a hydraulic characterization methodology of the backwashing process of sand filters used in micro irrigation, evaluating the influence of the sand particle size, the filter bed height, and the sand filter design. The proposed methodology can assist manufacturers in gathering equipment operating information, aiming at its presentation in the product catalogs.•This method article discusses a method of hydraulic evaluation of the backwashing process of sand filters used in micro irrigation.•The method can assist sand filter manufacturers in the correct definition of the equipment's operating parameters.•The method shows the effectiveness of using the filter media pressure loss evaluation in the indirect definition of the minimum fluidisation velocity.
| S-EPMC7327839 | biostudies-literature
Project description:Advances in remote sensing combined with the emergence of sophisticated methods for large-scale data analytics from the field of data science provide new methods to model complex interactions in biological systems. Using a data-driven philosophy, insights from experts are used to corroborate the results generated through analytical models instead of leading the model design. Following such an approach, this study outlines the development and implementation of a whole-of-forest phenotyping system that incorporates spatial estimates of productivity across a large plantation forest. In large-scale plantation forestry, improving the productivity and consistency of future forests is an important but challenging goal due to the multiple interactions between biotic and abiotic factors, the long breeding cycle, and the high variability of growing conditions. Forest phenotypic expression is highly affected by the interaction of environmental conditions and forest management but the understanding of this complex dynamics is incomplete. In this study, we collected an extensive set of 2.7 million observations composed of 62 variables describing climate, forest management, tree genetics, and fine-scale terrain information extracted from environmental surfaces, management records, and remotely sensed data. Using three machine learning methods, we compared models of forest productivity and evaluate the gain and Shapley values for interpreting the influence of categorical variables on the power of these methods to predict forest productivity at a landscape level. The most accurate model identified that the most important drivers of productivity were, in order of importance, genetics, environmental conditions, leaf area index, topology, and soil properties, thus describing the complex interactions of the forest. This approach demonstrates that new methods in remote sensing and data science enable powerful, landscape-level understanding of forest productivity. The phenotyping method developed here can be used to identify superior and inferior genotypes and estimate a productivity index for individual site. This approach can improve tree breeding and deployment of the right genetics to the right site in order to increase the overall productivity across planted forests.
| S-EPMC7068454 | biostudies-literature
Project description:Heterogeneous treatment effect (HTE) analysis focuses on examining varying treatment effects for individuals or subgroups in a population. For example, an HTE-informed understanding can critically guide physicians to individualize the medical treatment for a certain disease. However, HTE analysis has not been widely recognized and used, even given the explosive increase of data availability attributed to the arrival of the Big Data era. Part of the reason behind its underuse is that data are often of high dimension and high complexity, which pose significant challenges for applying conventional HTE analysis methods. To meet these challenges, a newly developed causal forest HTE method has been derived from the random forest machine-learning algorithm. We conducted a systematic performance evaluation for the causal forest method against the conventional two-step method by simulating scenarios with different levels of complexity for the analysis. Our results show that causal forest outperforms the conventional HTE method in assessing treatment effect, especially when data are complex (e.g., nonlinear) and high dimensional, suggesting that causal forest is a promising tool for real-world applications of HTE analysis.
| S-EPMC8592515 | biostudies-literature
Project description:Recent advancements in deep learning for automated image processing and classification have accelerated many new applications for medical image analysis. However, most deep learning algorithms have been developed using reconstructed, human-interpretable medical images. While image reconstruction from raw sensor data is required for the creation of medical images, the reconstruction process only uses a partial representation of all the data acquired. Here, we report the development of a system to directly process raw computed tomography (CT) data in sinogram-space, bypassing the intermediary step of image reconstruction. Two classification tasks were evaluated for their feasibility of sinogram-space machine learning: body region identification and intracranial hemorrhage (ICH) detection. Our proposed SinoNet, a convolutional neural network optimized for interpreting sinograms, performed favorably compared to conventional reconstructed image-space-based systems for both tasks, regardless of scanning geometries in terms of projections or detectors. Further, SinoNet performed significantly better when using sparsely sampled sinograms than conventional networks operating in image-space. As a result, sinogram-space algorithms could be used in field settings for triage (presence of ICH), especially where low radiation dose is desired. These findings also demonstrate another strength of deep learning where it can analyze and interpret sinograms that are virtually impossible for human experts.
| S-EPMC6820559 | biostudies-literature
Project description:With the rise in whole slide scanner technology, large numbers of tissue slides are being scanned and represented and archived digitally. While digital pathology has substantial implications for telepathology, second opinions, and education there are also huge research opportunities in image computing with this new source of "big data". It is well known that there is fundamental prognostic data embedded in pathology images. The ability to mine "sub-visual" image features from digital pathology slide images, features that may not be visually discernible by a pathologist, offers the opportunity for better quantitative modeling of disease appearance and hence possibly improved prediction of disease aggressiveness and patient outcome. However the compelling opportunities in precision medicine offered by big digital pathology data come with their own set of computational challenges. Image analysis and computer assisted detection and diagnosis tools previously developed in the context of radiographic images are woefully inadequate to deal with the data density in high resolution digitized whole slide images. Additionally there has been recent substantial interest in combining and fusing radiologic imaging and proteomics and genomics based measurements with features extracted from digital pathology images for better prognostic prediction of disease aggressiveness and patient outcome. Again there is a paucity of powerful tools for combining disease specific features that manifest across multiple different length scales. The purpose of this review is to discuss developments in computational image analysis tools for predictive modeling of digital pathology images from a detection, segmentation, feature extraction, and tissue classification perspective. We discuss the emergence of new handcrafted feature approaches for improved predictive modeling of tissue appearance and also review the emergence of deep learning schemes for both object detection and tissue classification. We also briefly review some of the state of the art in fusion of radiology and pathology images and also combining digital pathology derived image measurements with molecular "omics" features for better predictive modeling. The review ends with a brief discussion of some of the technical and computational challenges to be overcome and reflects on future opportunities for the quantitation of histopathology.
| S-EPMC5556681 | biostudies-other
Project description:Adjuvants have long been critical components of vaccines, but the exact mechanisms of their action and precisely how they alter or enhance vaccine-induced immune responses are often unclear. In this study, we used broad immunoprofiling of antibody, cellular, and cytokine responses, combined with data integration and machine learning to gain insight into the impact of different adjuvant formulations on vaccine-induced immune responses. A Self-Assembling Protein Nanoparticles (SAPN) presenting the malarial circumsporozoite protein (CSP) was used as a model vaccine, adjuvanted with three different liposomal formulations: liposome plus Alum (ALFA), liposome plus QS21 (ALFQ), and both (ALFQA). Using a computational approach to integrate the immunoprofiling data, we identified distinct vaccine-induced immune responses and developed a multivariate model that could predict the adjuvant condition from immune response data alone with 92% accuracy (p = 0.003). The data integration also revealed that commonly used readouts (i.e. serology, frequency of T cells producing IFN-γ, IL2, TNFα) missed important differences between adjuvants. In summary, broad immune-profiling in combination with machine learning methods enabled the reliable and clear definition of immune signatures for different adjuvant formulations, providing a means for quantitatively characterizing the complex roles that adjuvants can play in vaccine-induced immunity. The approach described here provides a powerful tool for identifying potential immune correlates of protection, a prerequisite for the rational pairing of vaccines candidates and adjuvants.
| S-EPMC6269591 | biostudies-literature