Affiliation:
1. Department of Botany, Faculty of Science University of South Bohemia České Budějovice Czechia
2. Agriculture and Agri‐Food Canada (AAFC) Ottawa Ontario Canada
3. Centre for Functional Ecology, Department of Life Sciences University of Coimbra Coimbra Portugal
4. Department of Integrative Biology University of Guelph Guelph Ontario Canada
Abstract
AbstractFlow cytometry (FCM) is now the most widely used method to determine ploidy levels and genome size of plants. To get reliable estimates and allow reproducibility of measurements, the methodology should be standardized and follow the best practices in the field. In this article, we discuss instrument calibration and quality control and various instrument and acquisition settings (parameters, flow rate, number of events, scales, use of discriminators, peak positions). These settings must be decided before measurements because they determine the amount and quality of the data and thus influence all downstream analyses. We describe the two main approaches to raw data analysis (gating and histogram modeling), and we discuss their advantages and disadvantages. Finally, we provide a summary of best practice recommendations for data acquisition and raw data analysis in plant FCM.
Funder
Natural Sciences and Engineering Research Council of Canada
Programa Operacional Regional do Centro
Subject
Cell Biology,Histology,Pathology and Forensic Medicine
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献