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Interpretation of microbiota-based diagnostics by explaining individual classifier decisions.
Eck, A; Zintgraf, L M; de Groot, E F J; de Meij, T G J; Cohen, T S; Savelkoul, P H M; Welling, M; Budding, A E.
Afiliação
  • Eck A; Department of Medical Microbiology and Infection Control, VU University medical center, Amsterdam, The Netherlands. a.eckhauer@vumc.nl.
  • Zintgraf LM; Informatics Institute, University of Amsterdam, Amsterdam, The Netherlands.
  • de Groot EFJ; Department of Gastroenterology and Hepatology, VU University medical center, Amsterdam, The Netherlands.
  • de Meij TGJ; Department of Pediatric Gastroenterology, VU University medical center, Amsterdam, The Netherlands.
  • Cohen TS; Informatics Institute, University of Amsterdam, Amsterdam, The Netherlands.
  • Savelkoul PHM; Department of Medical Microbiology and Infection Control, VU University medical center, Amsterdam, The Netherlands.
  • Welling M; Department of Medical Microbiology, Maastricht University medical center, Maastricht, The Netherlands.
  • Budding AE; Informatics Institute, University of Amsterdam, Amsterdam, The Netherlands.
BMC Bioinformatics ; 18(1): 441, 2017 Oct 04.
Article em En | MEDLINE | ID: mdl-28978318
ABSTRACT

BACKGROUND:

The human microbiota is associated with various disease states and holds a great promise for non-invasive diagnostics. However, microbiota data is challenging for traditional diagnostic approaches It is high-dimensional, sparse and comprises of high inter-personal variation. State of the art machine learning tools are therefore needed to achieve this goal. While these tools have the ability to learn from complex data and interpret patterns therein that cannot be identified by humans, they often operate as black boxes, offering no insight into their decision-making process. In most cases, it is difficult to represent the learning of a classifier in a comprehensible way, which makes them prone to be mistrusted, or even misused, in a clinical environment. In this study, we aim to elucidate microbiota-based classifier decisions in a biologically meaningful context to allow their interpretation.

RESULTS:

We applied a method for explanation of classifier decisions on two microbiota datasets of increasing complexity gut versus skin microbiota samples, and inflammatory bowel disease versus healthy gut microbiota samples. The algorithm simulates bacterial species as being unknown to a pre-trained classifier, and measures its effect on the outcome. Consequently, each patient is assigned a unique quantitative estimation of which species in their microbiota defined the classification of their sample. The algorithm was able to explain the classifier decisions well, demonstrated by our validation method, and the explanations were biologically consistent with recent microbiota findings.

CONCLUSIONS:

Application of a method for explaining individual classifier decisions for complex microbiota analysis proved feasible and opens perspectives on personalized therapy. Providing an explanation to support a microbiota-based diagnosis could guide decisions of clinical microbiologists, and has the potential to increase their confidence in the outcome of such decision support systems. This may facilitate the development of new diagnostic applications.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Microbioma Gastrointestinal Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Microbioma Gastrointestinal Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article