Globální změny ve stratosféře středních šířek

Several phenomena in the middle latitude stratosphere are studied in the thesis. The reanalyses are utilized as a source of data for our study. Different reanalyses are compared each other and with observations and problems of reanalyses are shown. We are interested in connection between ozone, dynamics and other phenomena (Sudden Stratospheric Warmings, solar cycle, NAO etc.) in the stratosphere, mainly from 1979 to present using ERA-Interim, NCEP/NCAR reanalyses or satellite observations. The linear connection between total ozone difference and 100 hPa eddy heat flux is found in winter middle latitudes. Ozone trends in Europe and China are analysed. The meridional and zonal wind is also studied using MERRA reanalysis and model output (CCM SOCOL v3.0). The comparison of geographical distribution of geopotential height and meridional wind is done. Differences between MERRA and CCM SOCOL v3.0 has been observed for geopotential hight and meridional wind for winter season.V této práci studujeme několik fenoménů ve stratosféře středních šířek. Reanalýzy jsou využívány jako zdroj dat pro naši studii. Různé reanalýzy jsou srovnány vzájemně mezi sebou nebo také s pozorovanými daty. Zajímáme se o propojení ozónu, dynamiky stratosféry a dalších fenoménů (náhlá stratosférická oteplení, solární cyklus, NAO atd.) zvláště od roku 1979 do současnosti s využitím ERA- Interim, NCEP/NCAR reanalýz nebo satelitních pozorování. Lineární vztah mezi změnou celkového množství ozónu a 100 hPa eddy heat flux je ukázán v zimní sezóně. Trendy ozónu v Evropě a Číně jsou analyzovány. Je také studováno chování meridionálního a zonálního větru s využitím MERRA reanalýz nebo z modelových výstupů (CCM SOCOL v3.0). Srovnání geografického rozdělení geopotenciální výšky a meridionálního větru je ukázáno. Rozdíly mezi MERRA reanalýzou a CCM SOCOL v3.0 jsou pozorovány pro obě sledované veličiny hlavně v zimní sezóně.Department of Atmospheric PhysicsKatedra fyziky atmosféryFaculty of Mathematics and PhysicsMatematicko-fyzikální fakult

Simultaneous Tracking of Multiple Objects Using Fast Level Set-Like Algorithm

A topological flexibility of implicit active contours is of great benefit, since it allows simultaneous detection of several objects without any a priori knowledge about their number and shapes. However, in tracking applications it is often required to keep desired objects mutually separated as well as allow each object to evolve itself, i.e., different objects cannot be merged together, but each object can split into several regions that can be merged again later in time. The former can be achieved by applying topology-preserving constraints exploiting either various repelling forces or the simple point concept from digital geometry, which brings, however, an indispensable increase in the execution time and also prevent the latter. In this paper, we propose more efficient and more flexible topology-preserving constraint based on a region indication function, that can be easily integrated into a fast level set-like algorithm [Maska, Matula, Danek, Kozubek, LNCS 6455, 2010] in order to obtain a fast and robust algorithm for simultaneous tracking of multiple objects. The potential of the modified algorithm is demonstrated on both synthetic and real image data

Prediction of localization and interactions of apoptotic proteins

During apoptosis several mitochondrial proteins are released. Some of them participate in caspase-independent nuclear DNA degradation, especially apoptosis-inducing factor (AIF) and endonuclease G (endoG). Another interesting protein, which was expected to act similarly as AIF due to the high sequence homology with AIF is AIF-homologous mitochondrion-associated inducer of death (AMID). We studied the structure, cellular localization, and interactions of several proteins in silico and also in cells using fluorescent microscopy. We found the AMID protein to be cytoplasmic, most probably incorporated into the cytoplasmic side of the lipid membranes. Bioinformatic predictions were conducted to analyze the interactions of the studied proteins with each other and with other possible partners. We conducted molecular modeling of proteins with unknown 3D structures. These models were then refined by MolProbity server and employed in molecular docking simulations of interactions. Our results show data acquired using a combination of modern in silico methods and image analysis to understand the localization, interactions and functions of proteins AMID, AIF, endonuclease G, and other apoptosis-related proteins

Toward a morphodynamic model of the cell: Signal processing for cell modeling

From a systems biology perspective, the cell is the principal element of information integration. Therefore, understanding the cell in its spatiotemporal context is the key to unraveling many of the still unknown mechanisms of life and disease. This article reviews image processing aspects relevant to the quantification of cell morphology and dynamics. We cover both acquisition (hardware) and analysis (software) related issues, in a multiscale fashion, from the detection of cellular components to the description of the entire cell in relation to its extracellular environment. We then describe ongoing efforts to integrate all this vast and diverse information along with data about the biomechanics of the cell to create a credible model of cell morphology and behavior.Carlos Ortiz-de-Solorzano and Arrate Muñoz-Barrutia were supported by the Spanish Ministry of Economy and Competitiveness grants with reference DPI2012-38090-C03-02 and TEC2013-48552-C02, respectively. Michal Kozubek was supported by the Czech Science Foundation (302/12/G157)

BIAS: Transparent reporting of biomedical image analysis challenges

The number of biomedical image analysis challenges organized per year is steadily increasing. These international competitions have the purpose of benchmarking algorithms on common data sets, typically to identify the best method for a given problem. Recent research, however, revealed that common practice related to challenge reporting does not allow for adequate interpretation and reproducibility of results. To address the discrepancy between the impact of challenges and the quality (control), the Biomedical Image Analysis ChallengeS (BIAS) initiative developed a set of recommendations for the reporting of challenges. The BIAS statement aims to improve the transparency of the reporting of a biomedical image analysis challenge regardless of field of application, image modality or task category assessed. This article describes how the BIAS statement was developed and presents a checklist which authors of biomedical image analysis challenges are encouraged to include in their submission when giving a paper on a challenge into review. The purpose of the checklist is to standardize and facilitate the review process and raise interpretability and reproducibility of challenge results by making relevant information explicit

Characterization of three-dimensional cancer cell migration in mixed collagen-Matrigel scaffolds using microfluidics and image analysis

Microfluidic devices are becoming mainstream tools to recapitulate in vitro the behavior of cells and tissues. In this study, we use microfluidic devices filled with hydrogels of mixed collagen-Matrigel composition to study the migration of lung cancer cells under different cancer invasion microenvironments. We present the design of the microfluidic device, characterize the hydrogels morphologically and mechanically and use quantitative image analysis to measure the migration of H1299 lung adenocarcinoma cancer cells in different experimental conditions. Our results show the plasticity of lung cancer cell migration, which turns from mesenchymal in collagen only matrices, to lobopodial in collagen-Matrigel matrices that approximate the interface between a disrupted basement membrane and the underlying connective tissue. Our quantification of migration speed confirms a biphasic role of Matrigel. At low concentration, Matrigel facilitates migration, most probably by providing a supportive and growth factor retaining environment. At high concentration, Matrigel slows down migration, possibly due excessive attachment. Finally, we show that antibody-based integrin blockade promotes a change in migration phenotype from mesenchymal or lobopodial to amoeboid and analyze the effect of this change in migration dynamics, in regards to the structure of the matrix. In summary, we describe and characterize a robust microfluidic platform and a set of software tools that can be used to study lung cancer cell migration under different microenvironments and experimental conditions. This platform could be used in future studies, thus benefitting from the advantages introduced by microfluidic devices: precise control of the environment, excellent optical properties, parallelization for high throughput studies and efficient use of therapeutic drugs.We would like to acknowledge the support of the Spanish Ministry of Economy and Competitiveness, under grants number DPI2012-38090-C03-02 and DPI2015-64221-C2-2-R (COS), TEC2013-48552-C2-1-R, TEC2016-78052-R, TEC2015-73064-EXP (AMB) and the Torres Quevedo program PTQ-11-04778 (RP); the Spanish Ministry of Health (FIS PI13/02313) (AR); the Czech Science Foundation, under grant number 302/12/G157 (MK, MMaška); and the European Research Council (ERC) through project ERC-2012-StG 306751 (JMGA)

Advancing global & regional reanalyses

This report outlines the structure of and summarizes the recommendations made at the 5th International Conference on Reanalysis (ICR5), attended by 259 participants from 37 countries, in Rome (Italy), on 13-17 November 2017. It first summarizes the conference structure. Then, the key recommendations of ICR5 are given for the five main conference topics: production; observations (data rescue and preparation); data assimilation methods; quality assurance of reanalysis; and applications in science, services, and policymaking. Lastly, five high-level recommendations are proposed to managing agencies on how best to advance the field of reanalyses, which serves tens of thousands of users, via enhanced research, development, and operations

Metrics reloaded: Pitfalls and recommendations for image analysis validation

Increasing evidence shows that flaws in machine learning (ML) algorithm validation are an underestimated global problem. Particularly in automatic biomedical image analysis, chosen performance metrics often do not reflect the domain interest, thus failing to adequately measure scientific progress and hindering translation of ML techniques into practice. To overcome this, our large international expert consortium created Metrics Reloaded, a comprehensive framework guiding researchers in the problem-aware selection of metrics. Following the convergence of ML methodology across application domains, Metrics Reloaded fosters the convergence of validation methodology. The framework was developed in a multi-stage Delphi process and is based on the novel concept of a problem fingerprint - a structured representation of the given problem that captures all aspects that are relevant for metric selection, from the domain interest to the properties of the target structure(s), data set and algorithm output. Based on the problem fingerprint, users are guided through the process of choosing and applying appropriate validation metrics while being made aware of potential pitfalls. Metrics Reloaded targets image analysis problems that can be interpreted as a classification task at image, object or pixel level, namely image-level classification, object detection, semantic segmentation, and instance segmentation tasks. To improve the user experience, we implemented the framework in the Metrics Reloaded online tool, which also provides a point of access to explore weaknesses, strengths and specific recommendations for the most common validation metrics. The broad applicability of our framework across domains is demonstrated by an instantiation for various biological and medical image analysis use cases

Common Limitations of Image Processing Metrics:A Picture Story

While the importance of automatic image analysis is continuously increasing, recent meta-research revealed major flaws with respect to algorithm validation. Performance metrics are particularly key for meaningful, objective, and transparent performance assessment and validation of the used automatic algorithms, but relatively little attention has been given to the practical pitfalls when using specific metrics for a given image analysis task. These are typically related to (1) the disregard of inherent metric properties, such as the behaviour in the presence of class imbalance or small target structures, (2) the disregard of inherent data set properties, such as the non-independence of the test cases, and (3) the disregard of the actual biomedical domain interest that the metrics should reflect. This living dynamically document has the purpose to illustrate important limitations of performance metrics commonly applied in the field of image analysis. In this context, it focuses on biomedical image analysis problems that can be phrased as image-level classification, semantic segmentation, instance segmentation, or object detection task. The current version is based on a Delphi process on metrics conducted by an international consortium of image analysis experts from more than 60 institutions worldwide.Comment: This is a dynamic paper on limitations of commonly used metrics. The current version discusses metrics for image-level classification, semantic segmentation, object detection and instance segmentation. For missing use cases, comments or questions, please contact [email protected] or [email protected]. Substantial contributions to this document will be acknowledged with a co-authorshi