[en] Due to the relative transparency of its embryos and larvae, the zebrafish is an ideal model organism for bioimaging approaches in vertebrates. Novel microscope technologies allow the imaging of developmental processes in unprecedented detail, and they enable the use of complex image-based read-outs for high-throughput/high-content screening. Such applications can easily generate Terabytes of image data, the handling and analysis of which becomes a major bottleneck in extracting the targeted information. Here, we describe the current state of the art in computational image analysis in the zebrafish system. We discuss the challenges encountered when handling high-content image data, especially with regard to data quality, annotation, and storage. We survey methods for preprocessing image data for further analysis, and describe selected examples of automated image analysis, including the tracking of cells during embryogenesis, heartbeat detection, identification of dead embryos, recognition of tissues and anatomical landmarks, and quantification of behavioral patterns of adult fish. We review recent examples for applications using such methods, such as the comprehensive analysis of cell lineages during early development, the generation of a three-dimensional brain atlas of zebrafish larvae, and high-throughput drug screens based on movement patterns. Finally, we identify future challenges for the zebrafish image analysis community, notably those concerning the compatibility of algorithms and data formats for the assembly of modular analysis pipelines.
Research Center/Unit :
Giga-Systems Biology and Chemical Biology - ULiège
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Mikut, Ralf
Dickmeis, Thomas
Driever, Wolfgang
Geurts, Pierre ; Université de Liège - ULiège > Dép. d'électric., électron. et informat. (Inst.Montefiore) > Systèmes et modélisation
FEDER - Fonds Européen de Développement Régional Région wallonne: Direction générale opérationnelle de l'Economie, de l'Emploi & de la Recherche (DGO6)
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.
Bibliography
Detrich III HW, Westerfield M, Zon LI. The Zebrafish: Disease Models and Chemical Screens, third edition. Academic Press, Waltham, MA, 2011.
Yang LX, Ho NY, Alshut R, Legradi J, Weiss C, Reischl M, et al. Zebrafish embryos as models for embryotoxic and teratological effects of chemicals. Reprod Toxicol 2009;28:245-253.
Bakkers J. Zebrafish as a model to study cardiac development and human cardiac disease. Cardiovasc Res 2011;91:279-288.
Mione MC, Trede NS. The zebrafish as a model for cancer. Dis Model Mech 2010;3:517-23.
Flinn L, Bretaud S, Lo C, Ingham PW, Bandmann O. Zebrafish as a new animal model for movement disorders. J Neurochem 2008;106:1991-1997.
Luengo-Oroz MA, Ledesma-Carbayo MJ, Peyrieras N, Santos A. Image analysis for understanding embryo development: a bridge from microscopy to biological insights. Curr Opin Genet Dev 2011;21:630-637.
Keller PJ, Schmidt AD, Wittbrodt J, Stelzer EH. Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy. Science 2008;322:1065-1069.
Alshut R, Legradi J, Liebel U, Yang L, van Wezel J, Strahle U, et al. Methods for automated high-throughput toxicity testing using zebrafish embryos. Lect Notes Artif Intell 2010;6359:219-226.
Devarakonda R, Palanisamy G, Green JM, Wilson BE. Data sharing and retrieval using OAI-PMH. Earth Sci Inform 2011;4:1-5.
Taylor CF, Field D, Sansone SA, Aerts J, Apweiler R, Ashburner M, et al. Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project. Nat Biotechnol 2008;26:889-896.
Shamir L. Assessing the efficacy of low-level image content descriptors for computer-based fluorescence microscopy image analysis. J Microsc 2011;243:284-292.
Layton JB. Intro to Nested-RAID: RAID-01 and RAID-10. Linux Magazine, 2011, January 6.
Jejkal T, Hartmann V, Stotzka R, Otte J, Garcia A, van Wezel J, et al. LAMBDA - The LSDF Execution Framework for Data Intensive Applications. 20th Euromicro International Conference on Parallel, Distributed and Network- Based Processing (PDP), 2012. Available at: http://dx .doi.org/10.1109/PDP.2012.69
Selderslaghs IW, Hooyberghs J, De Coen W, Witters HE. Locomotor activity in zebrafish embryos: a new method to assess developmental neurotoxicity. Neurotoxicol Teratol 2010;32:460-471.
Alshut R, Legradi J, Mikut R, Strahle U, Reischl M. Robust Identification of Coagulated Zebrafish Eggs using Image Processing and Classification Techniques. 19 Workshop Computational Intelligence, pp. 9-21, 2009. Available at: http://digbib.ubka.uni-karlsruhe.de/volltexte/1000013551
Berghmans S, Hunt J, Roach A, Goldsmith P. Zebrafish offer the potential for a primary screen to identify a wide variety of potential anticonvulsants. Epilepsy Res 2007;75:18-28.
Bhat S, Liebling M. Cardiac Tissue and Erythrocyte Separation in Bright-field Microscopy Images of the Embryonic Zebrafish Heart for Motion Estimation. IEEE International Symposium on Biomedical Imaging: From Nano to Macro (ISBI), 2009. Available at: http://dx.doi .org/10.1109/ISBI.2009.5193155
Bourgine P, Cunderlik R, Drblikova-Stasova O, Mikula K, Peyrieras N, Remesikova M, et al. 4d embryogenesis image analysis using Pde methods of image processing. Kybernetika 2010;46:226-259.
Cachat J, Stewart A, Utterback E, Hart P, Gaikwad S, Wong K, et al. Three-dimensional neurophenotyping of adult zebrafish behavior. PLoS One 2011;6:e17597.
Cao Y, Semanchik N, Lee SH, Somlo S, Barbano PE, Coifman R, et al. Chemical modifier screen identifies HDAC inhibitors as suppressors of PKD models. Proc Natl Acad Sci U S A 2009;106:21819-21824.
Carvalho R, de Sonneville J, Stockhammer OW, Savage ND, Veneman WJ, Ottenhoff TH, et al. A high-throughput screen for tuberculosis progression. PLoS One 2011;6: e16779.
Castro C, Luengo-Oroz M, Desnoulez S, Duloquin L, Fernandez-de-Manuel L, Montagna S, et al. An Automatic Quantification and Registration Strategy to Create a Gene Expression Atlas of Zebrafish Embryogenesis. Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), 2009. Available at: http://dx.doi.org/10.1109/IEMBS.2009.5332436
Chan PK, Lin CC, Cheng SH. Noninvasive technique for measurement of heartbeat regularity in zebrafish (Danio rerio) embryos. BMC Biotechnol 2009;9:11.
Chen S, Zhu Y, Xia W, Xia S, Xu X. Automated analysis of zebrafish images for phenotypic changes in drug discovery. J Neurosci Methods 2011;200:229-236.
Creton R. Automated analysis of behavior in zebrafish larvae. Behav Brain Res 2009;203:127-136.
d'Alencon CA, Pena OA, Wittmann C, Gallardo VE, Jones RA, Loosli F, et al. A high-throughput chemically induced inflammation assay in zebrafish. BMC Biol 2010;8:151.
Dempsey WP, Fraser SE, Pantazis P. PhOTO zebrafish: a transgenic resource for in vivo lineage tracing during development and regeneration. PLoS One 2012;7: e32888.
Fangerau J, Hockendorf B, Wittbrodt J, Leitte H. Similarity Analysis of Cell Movements in Video Microscopy. IEEE Symposium on Biological Data Visualization (BioVis), 2012. Available at: http://dx.doi.org/10.1109/BioVis. 2012.6378595
Fink M, Callol-Massot C, Chu A, Ruiz-Lozano P, Izpisua Belmonte JC, Giles W, et al. A new method for detection and quantification of heartbeat parameters in Drosophila, zebrafish, and embryonic mouse hearts. Biotechniques 2009;46:101-113.
Gehrig J, Reischl M, Kalmar E, Ferg M, Hadzhiev Y, Zaucker A, et al. Automated high-throughput mapping of promoter-enhancer interactions in zebrafish embryos. Nat Methods 2009;6:911-916.
Graf SF, Hotzel S, Liebel U, Stemmer A, Knapp HF. Imagebased fluidic sorting system for automated zebrafish egg sorting into multiwell plates. J Lab Autom 2011;16:105-111.
Green J, Collins C, Kyzar EJ, Pham M, Roth A, Gaikwad S, et al. Automated high-throughput neurophenotyping of zebrafish social behavior. J Neurosci Methods 2012;210: 266-271.
Grossman L, Utterback E, Stewart A, Gaikwad S, Chung KM, Suciu C, et al. Characterization of behavioral and endocrine effects of LSD on zebrafish. Behav Brain Res 2010;214:277-284.
Irons TD, MacPhail RC, Hunter DL, Padilla S. Acute neuroactive drug exposures alter locomotor activity in larval zebrafish. Neurotoxicol Teratol 2010;32:84-90.
Jeanray N, Maree R, Pruvot B, Stern O, Geurts P, Wehenkel L, et al. Phenotype classification of zebrafish embryos by supervised learning. Toxicol Lett 2012;211:S152.
Kamali M, Day LJ, Brooks DH, Zhou X, O'Malley DM. Automated identification of neurons in 3D confocal datasets from zebrafish brainstem. J Microsc 2009;233:114-131.
Kanungo J, Lantz S, Paule MG. In vivo imaging and quantitative analysis of changes in axon length using transgenic zebrafish embryos. Neurotoxicol Teratol 2011;33:618-623.
Kato S, Nakagawa T, Ohkawa M, Muramoto K, Oyama O, Watanabe A, et al. A computer image processing system for quantification of zebrafish behavior. J Neurosci Methods 2004;134:1-7.
Kausler BX, Schiegg M, Andres B, Lindner M, Leitte H, Hufnagel L, et al. A Discrete Chain Graph Model for 3D+ t Cell Tracking with High Misdetection Robustness, 2012. Available at: http://dx.doi.org/10.1007/978-3-642-33712-3-11
Kokel D, Bryan J, Laggner C,White R, Cheung CY,Mateus R, et al. Rapid behavior-based identification of neuroactive small molecules in the zebrafish. Nat Chem Biol 2010;6:231-237.
Kokel D, Dunn T, Ahrens M, Alshut R, Cheung CY, Saint- Amant L, et al. Identification of non-visual photomotor response cells in the vertebrate hindbrain. J Neurosci 2013;33:3834-3841.
Kriva Z, Mikula K, Peyrieras N, Rizzi B, Sarti A, Stasova O. 3D early embryogenesis image filtering by nonlinear partial differential equations. Med Image Anal 2010;14:510-526.
Liu T, Lu J, Wang Y, Campbell WA, Huang L, Zhu J, et al. Computerized image analysis for quantitative neuronal phenotyping in zebrafish. J Neurosci Methods 2006;153: 190-202.
Liu T, Li G, Nie J, Tarokh A, Zhou X, Guo L, et al. An automated method for cell detection in zebrafish. Neuroinformatics 2008;6:5-21.
Liu R, Lin S, Rallo R, Zhao Y, Damoiseaux R, Xia T, et al. Automated phenotype recognition for zebrafish embryo based in vivo high throughput toxicity screening of engineered nano-materials. PLoS One 2012;7:e35014.
Lou X, Kaster F, Lindner M, Kausler B, Kothe U, Hockendorf B, et al. Deltr: digital embryo lineage tree reconstructor. IEEE International Symposium on Biomedical Imaging: From Nano to Macro, 2011. Available at: http://dx.doi.org/10.1109/ISBI.2011.5872698
Lou X. Biomedical Data Analysis with Prior Knowledge: Modeling and Learning: University of Heidelberg, 2011. Available at: http://nbn-resolving.de/ urn:nbn:de:bsz:16- opus-122945
Lou X, Hamprecht FA. Structured Learning for Cell Tracking. Twenty-Fifth Annual Conference on Neural Information Processing Systems (NIPS 2011), 2011. Available at: http://books.nips.cc/papers/files/nips24/NIPS2011-0766.pdf
Luengo-Oroz MA, Rubio-Guivernau JL, Faure E, Savy T, Duloquin L, Olivier N, et al. Methodology for reconstructing early zebrafish development from in vivo multiphoton microscopy. IEEE Transact Image Proc 2012;21:2335-2340.
Luengo-Oroz MA, Pastor D, Castro C, Faure E, Savy T, Lombardot B, et al. 3D + t Morphological processing: applications to embryogenesis image analysis. IEEE Transact Image Proc 2012;21:3518-3530.
Mandrell D, Truong L, Jephson C, Sarker MR, Moore A, Lang C, et al. Automated zebrafish chorion removal and single embryo placement: optimizing throughput of zebrafish developmental toxicity screens. J Lab Autom 2012;17:66-74.
Meijer AH, van der Sar AM, Cunha C, Lamers GE, Laplante MA, Kikuta H, et al. Identification and real-time imaging of a myc-expressing neutrophil population involved in inflammation and mycobacterial granuloma formation in zebrafish. Dev Comp Immunol 2008;32:36-49.
Mikula K, Peyrieras N, Remesikova M, Stasova O. Segmentation of 3D cell membrane images by PDE methods and its applications. Comput Biol Med 2011;41: 326-339.
Ocorr K, Fink M, Cammarato A, Bernstein S, Bodmer R. Semi-automated optical heartbeat analysis of small hearts. Journal of visualized experiments: JoVE 2009;31.
Ohn J, Liebling M. In vivo, High-throughput Imaging for Functional Characterization of the Embryonic Zebrafish Heart. IEEE International Symposium on Biomedical Imaging: From Nano to Macro, 2011. Available at: http://dx .doi.org/10.1109/ISBI.2011.5872696
Olivier N, Luengo-Oroz MA, Duloquin L, Faure E, Savy T, Veilleux I, et al. Cell lineage reconstruction of early zebrafish embryos using label-free nonlinear microscopy. Science 2010;329:967-971.
Pardo-Martin C, Chang TY, Koo BK, Gilleland CL, Wasserman SC, Yanik MF. High-throughput in vivo vertebrate screening. Nat Methods 2010;7:634-636.
Peravali R, Gehrig J, Giselbrecht S, Lutjohann DS, Hadzhiev Y, Muller F, et al. Automated feature detection and imaging for high-resolution screening of zebrafish embryos. Biotechniques 2011;50:319-324.
Pfriem A, Pylatiuk C, Alshut R, Ziegener B, Schulz S, Bretthauer G. A modular, low-cost robot for zebrafish handling. Engineering in Medicine and Biology Society (EMBC), 2012. Available at: http://dx.doi.org/10.1109/EMBC.2012. 6346097
Rihel J, Prober DA, Arvanites A, Lam K, Zimmerman S, Jang S, et al. Zebrafish behavioral profiling links drugs to biological targets and rest/wake regulation. Science 2010;327:348-351.
Ronneberger O, Liu K, Rath M, Ruebeta D, Mueller T, Skibbe H, et al. ViBE-Z: a framework for 3D virtual colocalization analysis in zebrafish larval brains. Nat Methods 2012;9:735-742.
Rubio-Guivernau JL, Gurchenkov V, Luengo-Oroz MA, Duloquin L, Bourgine P, Santos A, et al. Wavelet-based image fusion in multi-view three-dimensional microscopy. Bioinformatics 2012;28:238-245.
Saydmohammed M, Vollmer LL, Onuoha EO, Vogt A, Tsang M. A high-content screening assay in transgenic zebrafish identifies two novel activators of fgf signaling. Birth Defects Res Part C 2011;93:281-287.
Vogt A, Cholewinski A, Shen X, Nelson SG, Lazo JS, Tsang M, et al. Automated image-based phenotypic analysis in zebrafish embryos. Dev Dyn 2009;238:656-663.
Spomer W, Pfriem A, Alshut R, Just S, Pylatiuk C. Highthroughput screening of zebrafish embryos using automated heart detection and imaging. J Lab Automat 2012;17:435-442.
Stern O, Marée R, Aceto J, Jeanray N, Muller M, Wehenkel L, et al. Automatic localization of interest points in zebrafish images with tree-based methods. Pattern Recog Bioinform 2011:179-190.
Tay TL, Ronneberger O, Ryu S, Nitschke R, Driever W. Comprehensive catecholaminergic projectome analysis reveals single-neuron integration of zebrafish ascending and descending dopaminergic systems. Nat Commun 2011; 2:171.
Temerinac-Ott M, Ronneberger O, Ochs P, Driever W, Brox T, Burkhardt H. Multiview deblurring for 3-D images from light-sheet-based fluorescence microscopy. IEEE Transact Image Proc 2012;21:1863-1873.
Walker SL, Ariga J, Mathias JR, Coothankandaswamy V, Xie X, Distel M, et al. Automated reporter quantification in vivo: high-throughput screening method for reporterbased assays in zebrafish. PLoS One 2012;7:e29916.
Weger BD, Weger M, Nusser M, Brenner-Weiss G, Dickmeis T. A chemical screening system for glucocorticoid stress hormone signaling in an intact vertebrate. ACS Chem Biol 2012;7:1178-1183.
Wittmann C, Reischl M, Shah AH, Mikut R, Liebel U, Grabher C. Facilitating drug discovery: an automated highcontent inflammation assay in zebrafish. Journal of visualized experiments: JoVE 2012;65:e4203.
Xu X, Xu X, Huang X, Xia W, Xia S. A high-throughput analysis method to detect regions of interest and quantify zebrafish embryo images. J Biomol Screen 2010;15:1152-1159.
Zanella C, Campana M, Rizzi B, Melani C, Sanguinetti G, Bourgine P, et al. Cells segmentation from 3-D confocal images of early zebrafish embryogenesis. IEEE Transact Image Proc 2010;19:770-781.
Emmenlauer M, Ronneberger O, Ponti A, Schwarb P, Griffa A, Filippi A, et al. XuvTools: free, fast and reliable stitching of large 3D datasets. J Microsc 2009;233:42-60.
Huisken J, Swoger J, Del Bene F, Wittbrodt J, Stelzer EHK. Optical sectioning deep inside live embryos by selective plane illumination microscopy. Science 2004;305:1007.
Preibisch S, Saalfeld S, Schindelin J, Tomancak P. Software for bead-based registration of selective plane illumination microscopy data. Nat Methods 2010;7:418-419.
Liu Y, Yu Y. Interactive image segmentation based on level sets of probabilities. IEEE Transact Visualization Comput Graphics 2011;18:1.
Hockendorf B, Thumberger T, Wittbrodt J. Quantitative analysis of embryogenesis: a perspective for light sheet microscopy. Dev Cell 2012;23:1111-1120.
Meijering E, Dzyubachyk O, Smal I. Methods for cell and particle tracking. Methods Enzymol 2012;504:183-200.
Mikula K, Peyrieras N, Remesiková M, Smisek M. 4D numerical schemes for cell image segmentation and tracking. Finite Volumes for Complex Applications VI Problems & Perspectives, Springer Proceedings in Mathematics Volume 4, 2011, pp. 693-701.
Pan YA, Livet J, Sanes JR, Lichtman JW, Schier AF. Multicolor brainbow imaging in zebrafish. Cold Spring Harb Protoc 2011;2011:pdb prot5546.
Culic-Viskota J, Dempsey WP, Fraser SE, Pantazis P. Surface functionalization of barium titanate SHG nanoprobes for in vivo imaging in zebrafish. Nat Protoc 2012;7: 1618-1633.
Pantazis P, Maloney J, Wu D, Fraser SE. Second harmonic generating (SHG) nanoprobes for in vivo imaging. Proc Natl Acad Sci U S A 2010;107:14535-14540.
Kankaanpaa P, Paavolainen L, Tiitta S, Karjalainen M, Paivarinne J, Nieminen J, et al. BioImageXD: an open, general-purpose and high-throughput image-processing platform. Nat Methods 2012;9:683-689.
Kvilekval K, Fedorov D, Obara B, Singh A, Manjunath BS. Bisque: a platform for bioimage analysis and management. Bioinformatics 2010;26:544-552.
Carpenter A, Jones T, Lamprecht M, Clarke C, Kang I, Friman O, et al. CellProfiler: image analysis software for identifying and quantifying cell phenotypes. Genome Biol 2006;7:R100.
Marée R, Stevens B, Rollus L, Rocks N, Moles-Lopez X, Salmon I, et al. A Rich Internet Application for Remote Visualization and Collaborative Annotation of Digital Slide Images in Histology and Cytology. 12th European Congress on Telepathology and 5th International Congress on Virtual Microscopy, 2012.
Stegmaier J, Alshut R, Reischl M, Mikut R. Information fusion of image analysis, video object tracking, and data mining of biological images using the open source MATLAB toolbox Gait-CAD. Biomed Tech 2012;57:458-461.
de Chaumont F, Dallongeville S, Chenouard N, Herve N, Pop S, Provoost T, et al. Icy: an open bioimage informatics platform for extended reproducible research. Nat Methods 2012;9:690-696.
Schindelin J, Arganda-Carreras I, Frise E, Kaynig V, Longair M, Pietzsch T, et al. Fiji: an open-source platform for biological-image analysis. Nat Methods 2012;9:676-682.
Sommer C, Straehle C, Kothe U, Hamprecht FA. ilastik: Interactive Learning and Segmentation Toolkit. IEEE International Symposium on Biomedical Imaging: From Nano to Macro, 2011. Available at: http://dx.doi.org/ 10.1109/ISBI.2011.5872394
Berthold MR, Cebron N, Dill F, Gabriel TR, Kotter T, Meinl T, et al. KNIME: the konstanz information miner. In: Data Analysis, Machine Learning and Applications. Preisach, C, Burkhardt, H, Schmidt-Thieme, L, Decker R, (eds), Springer, 2008, pp. 319-326.
Allan C, Burel JM, Moore J, Blackburn C, Linkert M, Loynton S, et al. OMERO: flexible, model-driven data management for experimental biology. Nat Methods 2012; 9:245-253.
Mikut R, Reischl M. Data mining tools. Wires Data Min Knowl 2011;1:431-443.
Liu T,Nie J, Li G, Guo L,Wong ST. ZFIQ: a software package for zebrafish biology. Bioinformatics 2008;24:438-439.
Xia S, Zhu Y, Xu X, Xia W. Computational techniques in zebrafish image processing and analysis. J NeurosciMethods 2013;213:6-13.
Kanungo J, Cuevas E, Ali SF, Paule MG. Ketamine induces motor neuron toxicity and alters neurogenic and proneural gene expression in zebrafish. J Appl Toxicol 2013;33: 410-417.
Fowlkes CC, Hendriks CL, Keranen SV, Weber GH, Rubel O, Huang MY, et al. A quantitative spatiotemporal atlas of gene expression in the Drosophila blastoderm. Cell 2008;133: 364-374.
Peng H, Chung P, Long F, Qu L, Jenett A, Seeds AM, et al. BrainAligner: 3D registration atlases of Drosophila brains. Nat Methods 2011;8:493-500.
Ahrens MB, Li JM, Orger MB, Robson DN, Schier AF, Engert F, et al. Brain-wide neuronal dynamics during motor adaptation in zebrafish. Nature 2012;485:471-477.
Linkert M, Rueden CT, Allan C, Burel JM, Moore W, Patterson A, et al. Metadata matters: access to image data in the real world. J Cell Biol 2010;189:777-782.
Lynnes C, Mack R. KDD services at the Goddard earth sciences distributed active archive center. In: Data Mining for Scientific and Engineering Applications. Grossman, RL, Kamath, C, Kegelmeyer, P, Kumar, V, Namburu R, (eds), Springer, 2001, pp. 165-181.
Shvachko K, Kuang H, Radia S, Chansler R. The Hadoop Distributed File System. IEEE 26th Symposium on Mass Storage Systems and Technologies (MSST), 2010. Available at: http://dx.doi.org/10.1109/MSST.2010.5496972
Meijering E, de Chaumont F, Smal I, Chenouard N, Maska M, Olivo-Marin JC. The 2012 Particle Tracking Challenge: An Objective Comparison of Particle Tracking Methods. BioImage Informatics Conference (BII 2012), Dresden, 2012.
Cavodeassi F, Bene FD, Furthauer M, Grabher C, Herzog W, Lehtonen S, et al. Report of the 2nd European Zebrafish Principal Investigator Meeting in Karlsruhe, Germany, March 21-24, 2012. Zebrafish 2013;10:119-123.
Similar publications
Sorry the service is unavailable at the moment. Please try again later.
This website uses cookies to improve user experience. Read more
Save & Close
Accept all
Decline all
Show detailsHide details
Cookie declaration
About cookies
Strictly necessary
Performance
Strictly necessary cookies allow core website functionality such as user login and account management. The website cannot be used properly without strictly necessary cookies.
This cookie is used by Cookie-Script.com service to remember visitor cookie consent preferences. It is necessary for Cookie-Script.com cookie banner to work properly.
Performance cookies are used to see how visitors use the website, eg. analytics cookies. Those cookies cannot be used to directly identify a certain visitor.
Used to store the attribution information, the referrer initially used to visit the website
Cookies are small text files that are placed on your computer by websites that you visit. Websites use cookies to help users navigate efficiently and perform certain functions. Cookies that are required for the website to operate properly are allowed to be set without your permission. All other cookies need to be approved before they can be set in the browser.
You can change your consent to cookie usage at any time on our Privacy Policy page.