An Extensible and Portable Open Source Application for Image and Signal Analysis in Java
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Management of Large Sets of Image Data Capture, Databases, Image Processing, Storage, Visualization Karol Kozak
Management of large sets of image data Capture, Databases, Image Processing, Storage, Visualization Karol Kozak Download free books at Karol Kozak Management of large sets of image data Capture, Databases, Image Processing, Storage, Visualization Download free eBooks at bookboon.com 2 Management of large sets of image data: Capture, Databases, Image Processing, Storage, Visualization 1st edition © 2014 Karol Kozak & bookboon.com ISBN 978-87-403-0726-9 Download free eBooks at bookboon.com 3 Management of large sets of image data Contents Contents 1 Digital image 6 2 History of digital imaging 10 3 Amount of produced images – is it danger? 18 4 Digital image and privacy 20 5 Digital cameras 27 5.1 Methods of image capture 31 6 Image formats 33 7 Image Metadata – data about data 39 8 Interactive visualization (IV) 44 9 Basic of image processing 49 Download free eBooks at bookboon.com 4 Click on the ad to read more Management of large sets of image data Contents 10 Image Processing software 62 11 Image management and image databases 79 12 Operating system (os) and images 97 13 Graphics processing unit (GPU) 100 14 Storage and archive 101 15 Images in different disciplines 109 15.1 Microscopy 109 360° 15.2 Medical imaging 114 15.3 Astronomical images 117 15.4 Industrial imaging 360° 118 thinking. 16 Selection of best digital images 120 References: thinking. 124 360° thinking . 360° thinking. Discover the truth at www.deloitte.ca/careers Discover the truth at www.deloitte.ca/careers © Deloitte & Touche LLP and affiliated entities. Discover the truth at www.deloitte.ca/careers © Deloitte & Touche LLP and affiliated entities. -
Bioimage Analysis Tools
Bioimage Analysis Tools Kota Miura, Sébastien Tosi, Christoph Möhl, Chong Zhang, Perrine Paul-Gilloteaux, Ulrike Schulze, Simon Norrelykke, Christian Tischer, Thomas Pengo To cite this version: Kota Miura, Sébastien Tosi, Christoph Möhl, Chong Zhang, Perrine Paul-Gilloteaux, et al.. Bioimage Analysis Tools. Kota Miura. Bioimage Data Analysis, Wiley-VCH, 2016, 978-3-527-80092-6. hal- 02910986 HAL Id: hal-02910986 https://hal.archives-ouvertes.fr/hal-02910986 Submitted on 3 Aug 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 2 Bioimage Analysis Tools 1 2 3 4 5 6 Kota Miura, Sébastien Tosi, Christoph Möhl, Chong Zhang, Perrine Pau/-Gilloteaux, - Ulrike Schulze,7 Simon F. Nerrelykke,8 Christian Tischer,9 and Thomas Penqo'" 1 European Molecular Biology Laboratory, Meyerhofstraße 1, 69117 Heidelberg, Germany National Institute of Basic Biology, Okazaki, 444-8585, Japan 2/nstitute for Research in Biomedicine ORB Barcelona), Advanced Digital Microscopy, Parc Científic de Barcelona, dBaldiri Reixac 1 O, 08028 Barcelona, Spain 3German Center of Neurodegenerative -
Downloaded from the Cellprofiler Site [31] to Provide a Starting Point for New Analyses
Open Access Software2006CarpenteretVolume al. 7, Issue 10, Article R100 CellProfiler: image analysis software for identifying and quantifying comment cell phenotypes Anne E Carpenter*, Thouis R Jones*†, Michael R Lamprecht*, Colin Clarke*†, In Han Kang†, Ola Friman‡, David A Guertin*, Joo Han Chang*, Robert A Lindquist*, Jason Moffat*, Polina Golland† and David M Sabatini*§ reviews Addresses: *Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA. †Computer Sciences and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02142, USA. ‡Department of Radiology, Brigham and Women's Hospital, Boston, MA 02115, USA. §Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA. Correspondence: David M Sabatini. Email: [email protected] Published: 31 October 2006 Received: 15 September 2006 Accepted: 31 October 2006 reports Genome Biology 2006, 7:R100 (doi:10.1186/gb-2006-7-10-r100) The electronic version of this article is the complete one and can be found online at http://genomebiology.com/2006/7/10/R100 © 2006 Carpenter et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. deposited research Cell<p>CellProfiler, image analysis the software first free, open-source system for flexible and high-throughput cell image analysis is described.</p> Abstract Biologists can now prepare and image thousands of samples per day using automation, enabling chemical screens and functional genomics (for example, using RNA interference). Here we describe the first free, open-source system designed for flexible, high-throughput cell image analysis, research refereed CellProfiler. -
Cellprofiler: Image Analysis Software for Identifying and Quantifying Cell Phenotypes
CellProfiler: image analysis software for identifying and quantifying cell phenotypes The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Genome Biology. 2006 Oct 31;7(10):R100 As Published http://dx.doi.org/10.1186/gb-2006-7-10-r100 Publisher BioMed Central Ltd Version Final published version Citable link http://hdl.handle.net/1721.1/58762 Terms of Use Creative Commons Attribution Detailed Terms http://creativecommons.org/licenses/by/2.0 1 2 3 Table of Contents Getting Started: MaskImage . 96 Introduction . 6 Morph . 110 Installation . 7 OverlayOutlines . 111 Getting Started with CellProfiler . 9 PlaceAdjacent . 112 RescaleIntensity . 115 Resize . 116 Help: Rotate . 118 BatchProcessing . 11 Smooth . 122 Colormaps. .16 Subtract . 125 DefaultImageFolder . 17 SubtractBackground . 126 DefaultOutputFolder . 18 Tile.............................................127 DeveloperInfo . 19 FastMode . 28 MatlabCrash . 29 Object Processing modules: OutputFilename . 30 ClassifyObjects . 41 PixelSize . 31 ClassifyObjectsByTwoMeasurements . 42 Preferences. .32 ConvertToImage . 45 SkipErrors . 33 Exclude . 65 TechDiagnosis . 34 ExpandOrShrink . 66 FilterByObjectMeasurement . 71 IdentifyObjectsInGrid . 76 File Processing modules: IdentifyPrimAutomatic . 77 CreateBatchFiles . 51 IdentifyPrimManual . 83 ExportToDatabase . 68 IdentifySecondary . 84 ExportToExcel. .70 IdentifyTertiarySubregion. .88 LoadImages . 90 Relate . 113 LoadSingleImage . 94 LoadText. .95 RenameOrRenumberFiles . -
Bio-Formats Documentation Release 4.4.9
Bio-Formats Documentation Release 4.4.9 The Open Microscopy Environment October 15, 2013 CONTENTS I About Bio-Formats 2 1 Why Java? 4 2 Bio-Formats metadata processing 5 3 Help 6 3.1 Reporting a bug ................................................... 6 3.2 Troubleshooting ................................................... 7 4 Bio-Formats versions 9 4.1 Version history .................................................... 9 II User Information 23 5 Using Bio-Formats with ImageJ and Fiji 24 5.1 ImageJ ........................................................ 24 5.2 Fiji .......................................................... 25 5.3 Bio-Formats features in ImageJ and Fiji ....................................... 26 5.4 Installing Bio-Formats in ImageJ .......................................... 26 5.5 Using Bio-Formats to load images into ImageJ ................................... 28 5.6 Managing memory in ImageJ/Fiji using Bio-Formats ................................ 32 5.7 Upgrading the Bio-Formats importer for ImageJ to the latest trunk build ...................... 34 6 OMERO 39 7 Image server applications 40 7.1 BISQUE ....................................................... 40 7.2 OME Server ..................................................... 40 8 Libraries and scripting applications 43 8.1 Command line tools ................................................. 43 8.2 FARSIGHT ...................................................... 44 8.3 i3dcore ........................................................ 44 8.4 ImgLib ....................................................... -
Titel Untertitel
KNIME Image Processing Nycomed Chair for Bioinformatics and Information Mining Department of Computer and Information Science Konstanz University, Germany Why Image Processing with KNIME? KNIME UGM 2013 2 The “Zoo” of Image Processing Tools Development Processing UI Handling ImgLib2 ImageJ OMERO OpenCV ImageJ2 BioFormats MatLab Fiji … NumPy CellProfiler VTK Ilastik VIGRA CellCognition … Icy Photoshop … = Single, individual, case specific, incompatible solutions KNIME UGM 2013 3 The “Zoo” of Image Processing Tools Development Processing UI Handling ImgLib2 ImageJ OMERO OpenCV ImageJ2 BioFormats MatLab Fiji … NumPy CellProfiler VTK Ilastik VIGRA CellCognition … Icy Photoshop … → Integration! KNIME UGM 2013 4 KNIME as integration platform KNIME UGM 2013 5 Integration: What and How? KNIME UGM 2013 6 Integration ImgLib2 • Developed at MPI-CBG Dresden • Generic framework for data (image) processing algoritms and data-structures • Generic design of algorithms for n-dimensional images and labelings • http://fiji.sc/wiki/index.php/ImgLib2 → KNIME: used as image representation (within the data cells); basis for algorithms KNIME UGM 2013 7 Integration ImageJ/Fiji • Popular, highly interactive image processing tool • Huge base of available plugins • Fiji: Extension of ImageJ1 with plugin-update mechanism and plugins • http://rsb.info.nih.gov/ij/ & http://fiji.sc/ → KNIME: ImageJ Macro Node KNIME UGM 2013 8 Integration ImageJ2 • Next-generation version of ImageJ • Complete re-design of ImageJ while maintaining backwards compatibility • Based on ImgLib2 -
9. Biomedical Imaging Informatics Daniel L
9. Biomedical Imaging Informatics Daniel L. Rubin, Hayit Greenspan, and James F. Brinkley After reading this chapter, you should know the answers to these questions: 1. What makes images a challenging type of data to be processed by computers, as opposed to non-image clinical data? 2. Why are there many different imaging modalities, and by what major two characteristics do they differ? 3. How are visual and knowledge content in images represented computationally? How are these techniques similar to representation of non-image biomedical data? 4. What sort of applications can be developed to make use of the semantic image content made accessible using the Annotation and Image Markup model? 5. Describe four different types of image processing methods. Why are such methods assembled into a pipeline when creating imaging applications? 6. Give an example of an imaging modality with high spatial resolution. Give an example of a modality that provides functional information. Why are most imaging modalities not capable of providing both? 7. What is the goal in performing segmentation in image analysis? Why is there more than one segmentation method? 8. What are two types of quantitative information in images? What are two types of semantic information in images? How might this information be used in medical applications? 9. What is the difference between image registration and image fusion? Given an example of each. 1 9.1. Introduction Imaging plays a central role in the healthcare process. Imaging is crucial not only to health care, but also to medical communication and education, as well as in research. -
Bio-Formats Documentation Release 5.2.2
Bio-Formats Documentation Release 5.2.2 The Open Microscopy Environment September 12, 2016 CONTENTS I About Bio-Formats 2 1 Help 4 2 Bio-Formats versions 5 3 Why Java? 6 4 Bio-Formats metadata processing 7 4.1 Reporting a bug ................................................... 7 4.2 Version history .................................................... 8 II User Information 38 5 Using Bio-Formats with ImageJ and Fiji 39 5.1 ImageJ overview ................................................... 39 5.2 Fiji overview ..................................................... 41 5.3 Bio-Formats features in ImageJ and Fiji ....................................... 42 5.4 Installing Bio-Formats in ImageJ .......................................... 42 5.5 Using Bio-Formats to load images into ImageJ ................................... 44 5.6 Managing memory in ImageJ/Fiji using Bio-Formats ................................ 48 6 Command line tools 51 6.1 Command line tools introduction .......................................... 51 6.2 Displaying images and metadata ........................................... 52 6.3 Converting a file to different format ......................................... 54 6.4 Validating XML in an OME-TIFF .......................................... 56 6.5 Editing XML in an OME-TIFF ........................................... 57 6.6 List formats by domain ................................................ 58 6.7 List supported file formats .............................................. 58 6.8 Display file in ImageJ ............................................... -
Imagej User Guide Contents Release Notes for Imagej 1.46R Vii IJ 1.46R Noteworthy Viii
RevisedIJ 1.46r edition ImageJ UserUser Guide Guide ImageJImageJ/Fiji 1.46 ImageJ User Guide Contents Release Notes for ImageJ 1.46r vii IJ 1.46r Noteworthy viii Tiago Ferreira • Wayne Rasband IJ User Guide | Booklet 1 Macro Listings ix Conventions x I Getting Started 1 Introduction 1 2 Installing and Maintaining ImageJ2 2.1 ImageJDistributions.................................. 2 2.2 Related Software ................................... 3 2.3 ImageJ2 ........................................ 5 3 Getting Help5 3.1 Help on Image Analysis................................ 5 3.2 Help on ImageJ.................................... 6 II Working with ImageJ 4 Using Keyboard Shortcuts8 5 Finding Commands8 6 Undo and Redo9 7 Image Types and Formats 10 Tuesday 2nd October, 2012 8 Stacks, Virtual Stacks and Hyperstacks 12 9 Color Images 14 10 Selections 17 Foreword 10.1 Manipulating ROIs .................................. 18 10.2 Composite Selections................................. 19 The ImageJ User Guide provides a detailed overview of ImageJ (and inherently Fiji), 10.3 Selections With Sub-pixel Coordinates ....................... 19 the standard in scientific image analysis (see XXVI Focus on Bioimage Informatics). It was thought as a comprehensive, fully-searchable, self-contained, annotatable 11 Overlays 19 manual (see Conventions Used in this Guide). A HTML version is also available as 12 3D Volumes 21 well as printer-friendly booklets (see Guide Formats). Its latest version can always be obtained from http://imagej.nih.gov/ij/docs/guide. The source files are available 13 Settings and Preferences 22 through a Git version control repository at http://fiji.sc/guide.git. Given ImageJ’s heavy development this guide will always remain incomplete. All Im- ageJ users and developers are encouraged to contribute to the ImageJ documentation III Extending ImageJ resources (see Getting Involved). -
Cellprofiler and Cellprofiler Analyst Guide for Analyzing Droplets
1 CellProfiler and CellProfiler Analyst guide for analyzing droplets Start-up 1. Download the software Cellprofiler (CP) (version 3.1.8) and Cellprofiler Analysist (CPA) (version 2.2.1) here (https://cellprofiler.org/releases/). 2. Install the CP and CPA software in your computer. 3. Open CP software by double clicking on the CP icon (CPA will be used later). 4. Wait while the program is initialized. 5. A “welcome to CP!” window will appear in the foreground and the CP interface along with the CP terminal for scripting in the background. 6. Optional: You can now choose to download and directly load an example pipeline into CP by clicking the Load and example pipeline or click Download a template from the CP website to: a. See how the software operates in general with hands-on training b. Use an example pipeline for your own image analysis, if they are more suitable for your data. 7. After you are done reading and exploring the “welcome to CP!” window, either click x in the corner to remove it or – to minimize it. CP introduction 8. Now you can see the interface of CP. 9. When working in CP, it is best to have this window as “full screen”. 10. Pipeline and Modules: a. A pipeline is a processing set to be used for your images and consists of various modules that you can add, edit, delete, move etc. b. You always start with 4 standard modules in your pipeline (Images, Metadata, NamesAndTypes, and Groups). c. Your pipeline is always displayed to the left. -
A System Architecture in Multiple Views for an Image Processing Graphical User Interface
A System Architecture in Multiple Views for an Image Processing Graphical User Interface Roberto Wagner Santos Maciel, Michel S. Soares a and Daniel Oliveira Dantas b Departamento de Computac¸ao,˜ Universidade Federal de Sergipe, Sao˜ Cristov´ ao,˜ SE, Brazil Keywords: Software Architecture, Unified Modeling Language, 4+1 View Model, UML. Abstract: Medical images are important components in modern health institutions, used mainly as a diagnostic support tool to improve the quality of patient care. Researchers and software developers have difficulty when building solutions for segmenting, filtering and visualizing medical images due to the learning curve, complexity of in- stallation and use of image processing tools. VisionGL is an open source library that facilitates programming through the automatic generation of C++ wrapper code. The wrapper code is responsible for calling paral- lel image processing functions or shaders on CPUs using OpenCL, and on GPUs using OpenCL, GLSL and CUDA. An extension to support distributed processing, named VGLGUI, involves the creation of a client with a workflow editor and a server, capable of executing that workflow. This article presents a description of archi- tecture in multiple views, using the architectural standard ISO/IEC/IEEE 42010:2011, the 4+1 View Model of Software Architecture and the Unified Modeling Language (UML), for a visual programming language with parallel and distributed processing capabilities. 1 INTRODUCTION lutions in the clinical and hospital environment (Ukis et al., 2013; Franc¸a et al., 2017). Most tools do not Medical images are important components in modern allow the sharing of images, software and process- health institutions, used mainly as a diagnostic sup- ing resources. -
Advanced Light Microscopy Core Facilities: Balancing Service, Science and Career
MICROSCOPY RESEARCH AND TECHNIQUE 79:463–479 (2016) Advanced Light Microscopy Core Facilities: Balancing Service, Science and Career ELISA FERRANDO-MAY,1* HELLA HARTMANN,2 JURGEN€ REYMANN,3 NARIMAN ANSARI,4 NADINE UTZ,1 HANS-ULRICH FRIED,5 CHRISTIAN KUKAT,6 JAN PEYCHL,7 CHRISTIAN LIEBIG,8 STEFAN TERJUNG,9 VIBOR LAKETA,10 ANJE SPORBERT,11 STEFANIE WEIDTKAMP-PETERS,12 ASTRID SCHAUSS,13 14 15 WERNER ZUSCHRATTER, SERGIY AVILOV, AND THE GERMAN BIOIMAGING NETWORK 1Department of Biology, University of Konstanz, Bioimaging Center, Universitatsstrasse€ 10, Konstanz, 78464, Germany 2Technical University Dresden, Center for Regenerative Therapies, Light Microscopy Facility, Fetscherstraße 105, Dresden, 01307, Germany 3Heidelberg University, BioQuant, ViroQuant-CellNetworks RNAi Screening Facility, Im Neuenheimer Feld 267, & Heidelberg Center for Human Bioinformatics, IPMB, Im Neuenheimer Feld 364, Heidelberg, 69120, Germany 4Goethe University Frankfurt am Main, Buchmann Institute for Molecular Life Sciences, Physical Biology Group, Max-von-Laue-Str. 15, Frankfurt am Main 60438, Germany 5Deutsches Zentrum fur€ Neurodegenerative Erkrankungen, Core Facility and Services, Light Microscopy Facility, Ludwig-Erhard- Allee 2, Bonn, 53175, Germany 6Max Planck Institute for Biology of Ageing, FACS & Imaging Core Facility, Joseph-Stelzmann-Str. 9b, Koln,€ 50931, Koln,€ Germany 7Max Planck Institute for Molecular Cell Biology and Genetics, Light Microscopy Facility, Pfotenhauerstr. 108, Dresden, 01307, Germany 8Max Planck Institute for Developmental Biology,