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Analysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects How to cite this article: Finn WG, Carter KM, Raich R, Stoolman LM, Hero AO. Analysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects. Cytometry Part B 2009; 76B: 1–7.

dc.contributor.authorFinn, William G.en_US
dc.contributor.authorCarter, Kevin Michaelen_US
dc.contributor.authorRaich, Raviven_US
dc.contributor.authorStoolman, Lloyd M.en_US
dc.contributor.authorHero, Alfred O. IIIen_US
dc.date.accessioned2009-01-07T15:30:26Z
dc.date.available2010-03-01T21:10:27Zen_US
dc.date.issued2009-01en_US
dc.identifier.citationFinn, William G.; Carter, Kevin M.; Raich, Raviv; Stoolman, Lloyd M.; Hero, Alfred O. (2009). "Analysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects How to cite this article: Finn WG, Carter KM, Raich R, Stoolman LM, Hero AO. Analysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects. Cytometry Part B 2009; 76B: 1–7. ." Cytometry Part B: Clinical Cytometry 76B(1): 1-7. <http://hdl.handle.net/2027.42/61450>en_US
dc.identifier.issn1552-4949en_US
dc.identifier.issn1552-4957en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/61450
dc.description.abstractBackground Clinical flow cytometry typically involves the sequential interpretation of two-dimensional histograms, usually culled from six or more cellular characteristics, following initial selection (gating) of cell populations based on a different subset of these characteristics. We examined the feasibility of instead treating gated n -parameter clinical flow cytometry data as objects embedded in n -dimensional space using principles of information geometry via a recently described method known as Fisher Information Non-parametric Embedding (FINE). Methods After initial selection of relevant cell populations through an iterative gating strategy, we converted four color (six-parameter) clinical flow cytometry datasets into six-dimensional probability density functions, and calculated differences among these distributions using the Kullback-Leibler divergence (a measurement of relative distributional entropy shown to be an appropriate approximation of Fisher information distance in certain types of statistical manifolds). Neighborhood maps based on Kullback-Leibler divergences were projected onto two dimensional displays for comparison. Results These methods resulted in the effective unsupervised clustering of cases of acute lymphoblastic leukemia from cases of expansion of physiologic B-cell precursors (hematogones) within a set of 54 patient samples. Conclusions The treatment of flow cytometry datasets as objects embedded in high-dimensional space (as opposed to sequential two-dimensional analyses) harbors the potential for use as a decision-support tool in clinical practice or as a means for context-based archiving and searching of clinical flow cytometry data based on high-dimensional distribution patterns contained within stored list mode data. Additional studies will be needed to further test the effectiveness of this approach in clinical practice. © 2008 Clinical Cytometry Societyen_US
dc.format.extent336234 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCell & Developmental Biologyen_US
dc.titleAnalysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects How to cite this article: Finn WG, Carter KM, Raich R, Stoolman LM, Hero AO. Analysis of clinical flow cytometric immunophenotyping data by clustering on statistical manifolds: Treating flow cytometry data as high-dimensional objects. Cytometry Part B 2009; 76B: 1–7.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Pathology, University of Michigan, 1301 Catherine Road, Room M5242, Ann Arbor, MI 48109-0602en_US
dc.contributor.affiliationumDepartment of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationotherSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97331en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/61450/1/20435_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/cyto.b.20435en_US
dc.identifier.sourceCytometry Part B: Clinical Cytometryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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