| Literature DB >> 34214188 |
Glyn Nelson1, Ulrike Boehm2, Steve Bagley3, Peter Bajcsy4, Johanna Bischof5, Claire M Brown6, Aurélien Dauphin7, Ian M Dobbie8, John E Eriksson9, Orestis Faklaris10, Julia Fernandez-Rodriguez11, Alexia Ferrand12, Laurent Gelman13, Ali Gheisari14, Hella Hartmann14, Christian Kukat15, Alex Laude1, Miso Mitkovski16, Sebastian Munck17, Alison J North18, Tobias M Rasse19, Ute Resch-Genger20, Lucas C Schuetz21, Arne Seitz22, Caterina Strambio-De-Castillia23, Jason R Swedlow24, Ioannis Alexopoulos25, Karin Aumayr26, Sergiy Avilov27, Gert-Jan Bakker28, Rodrigo R Bammann29, Andrea Bassi30, Hannes Beckert31, Sebastian Beer32, Yury Belyaev33, Jakob Bierwagen34, Konstantin A Birngruber35, Manel Bosch36, Juergen Breitlow37, Lisa A Cameron38, Joe Chalfoun4, James J Chambers39, Chieh-Li Chen40, Eduardo Conde-Sousa41,42, Alexander D Corbett43, Fabrice P Cordelieres44, Elaine Del Nery45, Ralf Dietzel46, Frank Eismann47, Elnaz Fazeli48, Andreas Felscher49, Hans Fried50, Nathalie Gaudreault51, Wah Ing Goh52, Thomas Guilbert53, Roland Hadleigh29, Peter Hemmerich54, Gerhard A Holst55, Michelle S Itano56, Claudia B Jaffe57, Helena K Jambor58, Stuart C Jarvis59, Antje Keppler60, David Kirchenbuechler61, Marcel Kirchner15, Norio Kobayashi62, Gabriel Krens63, Susanne Kunis64, Judith Lacoste65, Marco Marcello66, Gabriel G Martins67, Daniel J Metcalf29, Claire A Mitchell68, Joshua Moore24, Tobias Mueller69, Michael S Nelson70, Stephen Ogg71, Shuichi Onami72, Alexandra L Palmer73, Perrine Paul-Gilloteaux74, Jaime A Pimentel75, Laure Plantard13, Santosh Podder76, Elton Rexhepaj77, Arnaud Royon78, Markku A Saari79, Damien Schapman80, Vincent Schoonderwoert81, Britta Schroth-Diez82, Stanley Schwartz83, Michael Shaw84, Martin Spitaler85, Martin T Stoeckl86, Damir Sudar87, Jeremie Teillon88, Stefan Terjung21, Roland Thuenauer89, Christian D Wilms29, Graham D Wright52, Roland Nitschke90.
Abstract
A modern day light microscope has evolved from a tool devoted to making primarily empirical observations to what is now a sophisticated , quantitative device that is an integral part of both physical and life science research. Nowadays, microscopes are found in nearly every experimental laboratory. However, despite their prevalent use in capturing and quantifying scientific phenomena, neither a thorough understanding of the principles underlying quantitative imaging techniques nor appropriate knowledge of how to calibrate, operate and maintain microscopes can be taken for granted. This is clearly demonstrated by the well-documented and widespread difficulties that are routinely encountered in evaluating acquired data and reproducing scientific experiments. Indeed, studies have shown that more than 70% of researchers have tried and failed to repeat another scientist's experiments, while more than half have even failed to reproduce their own experiments. One factor behind the reproducibility crisis of experiments published in scientific journals is the frequent underreporting of imaging methods caused by a lack of awareness and/or a lack of knowledge of the applied technique. Whereas quality control procedures for some methods used in biomedical research, such as genomics (e.g. DNA sequencing, RNA-seq) or cytometry, have been introduced (e.g. ENCODE), this issue has not been tackled for optical microscopy instrumentation and images. Although many calibration standards and protocols have been published, there is a lack of awareness and agreement on common standards and guidelines for quality assessment and reproducibility. In April 2020, the QUality Assessment and REProducibility for instruments and images in Light Microscopy (QUAREP-LiMi) initiative was formed. This initiative comprises imaging scientists from academia and industry who share a common interest in achieving a better understanding of the performance and limitations of microscopes and improved quality control (QC) in light microscopy. The ultimate goal of the QUAREP-LiMi initiative is to establish a set of common QC standards, guidelines, metadata models and tools, including detailed protocols, with the ultimate aim of improving reproducible advances in scientific research. This White Paper (1) summarizes the major obstacles identified in the field that motivated the launch of the QUAREP-LiMi initiative; (2) identifies the urgent need to address these obstacles in a grassroots manner, through a community of stakeholders including, researchers, imaging scientists, bioimage analysts, bioimage informatics developers, corporate partners, funding agencies, standards organizations, scientific publishers and observers of such; (3) outlines the current actions of the QUAREP-LiMi initiative and (4) proposes future steps that can be taken to improve the dissemination and acceptance of the proposed guidelines to manage QC. To summarize, the principal goal of the QUAREP-LiMi initiative is to improve the overall quality and reproducibility of light microscope image data by introducing broadly accepted standard practices and accurately captured image data metrics.Entities:
Keywords: confocal; light microscopy; metadata; quality assessment; quality control; reproducibility; widefield
Mesh:
Year: 2021 PMID: 34214188 DOI: 10.1111/jmi.13041
Source DB: PubMed Journal: J Microsc ISSN: 0022-2720 Impact factor: 1.952