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A large comparison of integrated SAR/QSAR models of the Ames test for mutagenicity($)

Benfenati, E. (författare)
Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milano, Italy
Golbamaki, A. (författare)
Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milano, Italy
Raitano, G. (författare)
Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milano, Italy
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Roncaglioni, A. (författare)
Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milano, Italy
Manganelli, S. (författare)
Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milano, Italy; Nestlé Research Center, Lausanne, Switzerland
Lemke, F. (författare)
KnowledgeMiner, Berlin, Germany
Norinder, Ulf (författare)
Stockholms universitet,Institutionen för data- och systemvetenskap,Swetox, Södertälje, Sweden; Dept of Computer and Systems Sciences, Stockholm University, Kista, Sweden
Lo Piparo, Elena (författare)
Nestlé Research Center, Lausanne, Switzerland
Honma, M. (författare)
National Institute of Health Sciences, Kawasaki, Japan
Manganaro, A. (författare)
KODE, Pisa, Italy
Gini, G. (författare)
Politecnico di Milano, Milano, Italy
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 (creator_code:org_t)
Taylor & Francis, 2018
2018
Engelska.
Ingår i: SAR and QSAR in environmental research (Print). - : Taylor & Francis. - 1062-936X .- 1029-046X. ; 29:8, s. 591-611
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Results from the Ames test are the first outcome considered to assess the possible mutagenicity of substances. Many QSAR models and structural alerts are available to predict this endpoint. From a regulatory point of view, the recommendation from international authorities is to consider the predictions of more than one model and to combine results in order to develop conclusions about the mutagenicity risk posed by chemicals. However, the results of those models are often conflicting, and the existing inconsistency in the predictions requires intelligent strategies to integrate them. In our study, we evaluated different strategies for combining results of models for Ames mutagenicity, starting from a set of 10 diverse individual models, each built on a dataset of around 6000 compounds. The novelty of our study is that we collected a much larger set of about 18,000 compounds and used the new data to build a family of integrated models. These integrations used probabilistic approaches, decision theory, machine learning, and voting strategies in the integration scheme. Results are discussed considering balanced or conservative perspectives, regarding the possible uses for different purposes, including screening of large collection of substances for prioritization.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Data- och informationsvetenskap (hsv//swe)
NATURAL SCIENCES  -- Computer and Information Sciences (hsv//eng)
NATURVETENSKAP  -- Geovetenskap och miljövetenskap (hsv//swe)
NATURAL SCIENCES  -- Earth and Related Environmental Sciences (hsv//eng)
NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Nyckelord

prediction of mutagenicity
Ames test
ensembles of models
integrating SAR and QSAR
naive Bayes
Dempster-Shafer theory
self-organizing neural networks
GMDH

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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