INSTITUTO TECNOLOGICO DE CHASCOMUS
Unidad Ejecutora - UE
flowDiv: a new pipeline for analyzing flow cytometric diversity
WANDERLEY, BRUNO M. S.; AMADO, ANDRÉ M.; METZ, SEBASTIÁN D.; A. ARAÚJO, DANIEL S.; NETO, ADRIÃO D. D.; UNREIN, FERNANDO; A. ARAÚJO, DANIEL S.; NETO, ADRIÃO D. D.; UNREIN, FERNANDO; QUIROGA, MARÍA V.; SARMENTO, HUGO; QUIROGA, MARÍA V.; SARMENTO, HUGO; WANDERLEY, BRUNO M. S.; AMADO, ANDRÉ M.; METZ, SEBASTIÁN D.
BIOMED CENTRAL LTD
Año: 2019 vol. 20
Background: Flow cytometry (FCM) is one of the most commonly used technologies for analysis of numerous biological systems at the cellular level, from cancer cells to microbial communities. Its high potential and wide applicability led to the development of various analytical protocols, which are often not interchangeable between fields of expertise. Environmental science in particular faces difficulty in adapting to non-specific protocols, mainly because of the highly heterogeneous nature of environmental samples. This variety, although it is intrinsic to environmental studies, makes it difficult to adjust analytical protocols to maintain both mathematical formalism and comprehensible biological interpretations, principally for questions that rely on the evaluation of differences between cytograms, an approach also termed cytometric diversity. Despite the availability of promising bioinformatic tools conceived for or adapted to cytometric diversity, most of them still cannot deal with common technical issues such as the integration of differently acquired datasets, the optimal number of bins, and the effective correlation of bins to previously known cytometric populations.Results: To address these and other questions, we have developed flowDiv, an R language pipeline for analysis of environmental flow cytometry data. Here, we present the rationale for flowDiv and apply the method to a real dataset from 31 freshwater lakes in Patagonia, Argentina, to reveal significant aspects of their cytometric diversities. Conclusions: flowDiv provides a rather intuitive way of proceeding with FCM analysis, as it combines formal mathematical solutions and biological rationales in an intuitive framework specifically designed to explore cytometric diversity.