Traditional methods for flow cytometry (FCM) data processing rely on subjective manual gating. Recently, several groups have developed computational methods for identifying cell populations in multidimensional FCM data. The Flow Cytometry: Critical Assessment of Population Identification Methods (FlowCAP) challenges were established to compare the performance of these methods on two tasks: (i) mammalian cell population identification, to determine whether automated algorithms can reproduce expert manual gating and (ii) sample classification, to determine whether analysis pipelines can identify characteristics that correlate with external variables (such as clinical outcome). This analysis presents the results of the first FlowCAP challenges. Several methods performed well as compared to manual gating or external variables using statistical performance measures, which suggests that automated methods have reached a sufficient level of maturity and accuracy for reliable use in FCM data analysis.

Critical assessment of automated flow cytometry data analysis techniques

Di Camillo B;Sanavia T;
2013-01-01

Abstract

Traditional methods for flow cytometry (FCM) data processing rely on subjective manual gating. Recently, several groups have developed computational methods for identifying cell populations in multidimensional FCM data. The Flow Cytometry: Critical Assessment of Population Identification Methods (FlowCAP) challenges were established to compare the performance of these methods on two tasks: (i) mammalian cell population identification, to determine whether automated algorithms can reproduce expert manual gating and (ii) sample classification, to determine whether analysis pipelines can identify characteristics that correlate with external variables (such as clinical outcome). This analysis presents the results of the first FlowCAP challenges. Several methods performed well as compared to manual gating or external variables using statistical performance measures, which suggests that automated methods have reached a sufficient level of maturity and accuracy for reliable use in FCM data analysis.
2013
10
3
228
238
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906045/pdf/41592_2013_Article_BFnmeth2365.pdf
Computational biology and bioinformatics, Immunology, Cancer, Flow cytometry
Aghaeepour N; Finak G; FlowCAP Consortium; Dougall D; Khodabakhshi AH; Mah P; Obermoser G; Spidlen J; Taylor I; Wuensch SA; Bramson J; Eaves C; Weng AP; Iii ES; Ho K; Kollmann T; Rogers W; De Rosa S; Dalal B; Azad A; Pothen A; Brandes A; Bretschneider H; Bruggner R; Finck R; Jia R; Zimmerman N; Linderman M; Dill D; Nolan G; Chan C; Khettabi FE; O'Neill K; Chikina M; Ge Y; Sealfon S; Sugár I; Gupta A; Shooshtari P; Zare H; De Jager PL; Jiang M; Keilwagen J; Maisog JM; Luta G; Barbo AA; Májek P; Vilček J; Manninen T; Huttunen H; Ruusuvuori P; Nykter M; McLachlan GJ; Wang K; Naim I; Sharma G; Nikolic R; Pyne S; Qian Y; Qiu P; Quinn J; Roth A; DREAM Consortium; Meyer P; Stolovitzky G; Saez-Rodriguez J; Norel R; Bhattacharjee M; Biehl M; Bucher P; Bunte K; Di Camillo B; Sambo F; Sanavia T; Trifoglio E; Toffolo G; Dimitrieva S; Dreos R; Ambrosini G; Grau J; Grosse I; Posch S; Guex N; Keilwagen J; Kursa M; Rudnicki W; Liu B; Maienschein-Cline M; Manninen T; Huttunen H; Ruusuvuori P; Nykter M; Schneider P; Seifert M; Strickert M; Vilar JM; Hoos H; Mosmann TR; Brinkman R; Gottardo R; Scheuermann RH
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1727799
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