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Predicting Phospholipidosis Using Machine Learning
[Image: see text] Phospholipidosis is an adverse effect caused by numerous cationic amphiphilic drugs and can affect many cell types. It is characterized by the excess accumulation of phospholipids and is most reliably identified by electron microscopy of cells revealing the presence of lamellar inc...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949053/ https://www.ncbi.nlm.nih.gov/pubmed/20799726 http://dx.doi.org/10.1021/mp100103e |
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author | Lowe, Robert Glen, Robert C. Mitchell, John B. O. |
author_facet | Lowe, Robert Glen, Robert C. Mitchell, John B. O. |
author_sort | Lowe, Robert |
collection | PubMed |
description | [Image: see text] Phospholipidosis is an adverse effect caused by numerous cationic amphiphilic drugs and can affect many cell types. It is characterized by the excess accumulation of phospholipids and is most reliably identified by electron microscopy of cells revealing the presence of lamellar inclusion bodies. The development of phospholipidosis can cause a delay in the drug development process, and the importance of computational approaches to the problem has been well documented. Previous work on predictive methods for phospholipidosis showed that state of the art machine learning methods produced the best results. Here we extend this work by looking at a larger data set mined from the literature. We find that circular fingerprints lead to better models than either E-Dragon descriptors or a combination of the two. We also observe very similar performance in general between Random Forest and Support Vector Machine models. |
format | Text |
id | pubmed-2949053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-29490532010-10-04 Predicting Phospholipidosis Using Machine Learning Lowe, Robert Glen, Robert C. Mitchell, John B. O. Mol Pharm [Image: see text] Phospholipidosis is an adverse effect caused by numerous cationic amphiphilic drugs and can affect many cell types. It is characterized by the excess accumulation of phospholipids and is most reliably identified by electron microscopy of cells revealing the presence of lamellar inclusion bodies. The development of phospholipidosis can cause a delay in the drug development process, and the importance of computational approaches to the problem has been well documented. Previous work on predictive methods for phospholipidosis showed that state of the art machine learning methods produced the best results. Here we extend this work by looking at a larger data set mined from the literature. We find that circular fingerprints lead to better models than either E-Dragon descriptors or a combination of the two. We also observe very similar performance in general between Random Forest and Support Vector Machine models. American Chemical Society 2010-08-27 2010-10-04 /pmc/articles/PMC2949053/ /pubmed/20799726 http://dx.doi.org/10.1021/mp100103e Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Lowe, Robert Glen, Robert C. Mitchell, John B. O. Predicting Phospholipidosis Using Machine Learning |
title | Predicting Phospholipidosis Using Machine Learning |
title_full | Predicting Phospholipidosis Using Machine Learning |
title_fullStr | Predicting Phospholipidosis Using Machine Learning |
title_full_unstemmed | Predicting Phospholipidosis Using Machine Learning |
title_short | Predicting Phospholipidosis Using Machine Learning |
title_sort | predicting phospholipidosis using machine learning |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949053/ https://www.ncbi.nlm.nih.gov/pubmed/20799726 http://dx.doi.org/10.1021/mp100103e |
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