Evidence map›Paper›PMID 26040910›Full record

ArticleBiostatistics (Oxford, England)2016

Discriminative variable subsets in Bayesian classification with mixture models, with application in flow cytometry studies.

Lin Lin, Cliburn Chan, Mike West

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Lin LinVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA llin@fredhutch.org.
Cliburn ChanBiostatistics & Bioinformatics, Duke University Medical Center, Durham, NC 27710-2721, and Department of Statistical Science, Duke University, Durham, NC 27708-0251, USA.
Mike WestDepartment of Statistical Science, Duke University, Durham, NC 27708-0251, USA.

Funding

Immune profiling of multi-parameter flow cytometry using computational statisticsRC1AI086032 · NIAID · DUKE UNIVERSITY · PI CHAN, CLIBURN C · 2009 to 2010
$977k
NIAID NIH HHS P30-AI06451NIAID NIH HHS RC1-AI086032
6 · The paper itself

Abstract

We discuss the evaluation of subsets of variables for the discriminative evidence they provide in multivariate mixture modeling for classification. The novel development of Bayesian classification analysis presented is partly motivated by problems of design and selection of variables in biomolecular studies, particularly involving widely used assays of large-scale single-cell data generated using flow cytometry technology. For such studies and for mixture modeling generally, we define discriminative analysis that overlays fitted mixture models using a natural measure of concordance between mixture component densities, and define an effective and computationally feasible method for assessing and prioritizing subsets of variables according to their roles in discrimination of one or more mixture components. We relate the new discriminative information measures to Bayesian classification probabilities and error rates, and exemplify their use in Bayesian analysis of Dirichlet process mixture models fitted via Markov chain Monte Carlo methods as well as using a novel Bayesian expectation-maximization algorithm. We present a series of theoretical and simulated data examples to fix concepts and exhibit the utility of the approach, and compare with prior approaches. We demonstrate application in the context of automatic classification and discriminative variable selection in high-throughput systems biology using large flow cytometry datasets.

Indexed as

Bayes TheoremModels, StatisticalFlow CytometryHumansT-Lymphocytes, RegulatoryBayesian expectation–maximizationBayesian mixture modelsClassification error ratesConcordance of densitiesDirichlet process mixturesDiscriminative information measureDiscriminative threshold probabilitiesFlow cytometry dataNon-Gaussian component mixturesVariable subset selection

Identifiers

PMID26040910
PMCPMC4679067

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.