Multi-label multi-kernel transfer learning for human protein subcellular localization.

Recent years have witnessed much progress in computational modelling for protein subcellular localization. However, the existing sequence-based predictive models demonstrate moderate or unsatisfactory performance, and the gene ontology (GO) based models may take the risk of performance overestimatio...

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Main Author: Suyu Mei
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3374840?pdf=render
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spelling doaj-c9b73c9d88ef46669fba84fafb7f543c2020-11-25T01:56:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3771610.1371/journal.pone.0037716Multi-label multi-kernel transfer learning for human protein subcellular localization.Suyu MeiRecent years have witnessed much progress in computational modelling for protein subcellular localization. However, the existing sequence-based predictive models demonstrate moderate or unsatisfactory performance, and the gene ontology (GO) based models may take the risk of performance overestimation for novel proteins. Furthermore, many human proteins have multiple subcellular locations, which renders the computational modelling more complicated. Up to the present, there are far few researches specialized for predicting the subcellular localization of human proteins that may reside in multiple cellular compartments. In this paper, we propose a multi-label multi-kernel transfer learning model for human protein subcellular localization (MLMK-TLM). MLMK-TLM proposes a multi-label confusion matrix, formally formulates three multi-labelling performance measures and adapts one-against-all multi-class probabilistic outputs to multi-label learning scenario, based on which to further extends our published work GO-TLM (gene ontology based transfer learning model for protein subcellular localization) and MK-TLM (multi-kernel transfer learning based on Chou's PseAAC formulation for protein submitochondria localization) for multiplex human protein subcellular localization. With the advantages of proper homolog knowledge transfer, comprehensive survey of model performance for novel protein and multi-labelling capability, MLMK-TLM will gain more practical applicability. The experiments on human protein benchmark dataset show that MLMK-TLM significantly outperforms the baseline model and demonstrates good multi-labelling ability for novel human proteins. Some findings (predictions) are validated by the latest Swiss-Prot database. The software can be freely downloaded at http://soft.synu.edu.cn/upload/msy.rar.http://europepmc.org/articles/PMC3374840?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Suyu Mei
spellingShingle Suyu Mei
Multi-label multi-kernel transfer learning for human protein subcellular localization.
PLoS ONE
author_facet Suyu Mei
author_sort Suyu Mei
title Multi-label multi-kernel transfer learning for human protein subcellular localization.
title_short Multi-label multi-kernel transfer learning for human protein subcellular localization.
title_full Multi-label multi-kernel transfer learning for human protein subcellular localization.
title_fullStr Multi-label multi-kernel transfer learning for human protein subcellular localization.
title_full_unstemmed Multi-label multi-kernel transfer learning for human protein subcellular localization.
title_sort multi-label multi-kernel transfer learning for human protein subcellular localization.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Recent years have witnessed much progress in computational modelling for protein subcellular localization. However, the existing sequence-based predictive models demonstrate moderate or unsatisfactory performance, and the gene ontology (GO) based models may take the risk of performance overestimation for novel proteins. Furthermore, many human proteins have multiple subcellular locations, which renders the computational modelling more complicated. Up to the present, there are far few researches specialized for predicting the subcellular localization of human proteins that may reside in multiple cellular compartments. In this paper, we propose a multi-label multi-kernel transfer learning model for human protein subcellular localization (MLMK-TLM). MLMK-TLM proposes a multi-label confusion matrix, formally formulates three multi-labelling performance measures and adapts one-against-all multi-class probabilistic outputs to multi-label learning scenario, based on which to further extends our published work GO-TLM (gene ontology based transfer learning model for protein subcellular localization) and MK-TLM (multi-kernel transfer learning based on Chou's PseAAC formulation for protein submitochondria localization) for multiplex human protein subcellular localization. With the advantages of proper homolog knowledge transfer, comprehensive survey of model performance for novel protein and multi-labelling capability, MLMK-TLM will gain more practical applicability. The experiments on human protein benchmark dataset show that MLMK-TLM significantly outperforms the baseline model and demonstrates good multi-labelling ability for novel human proteins. Some findings (predictions) are validated by the latest Swiss-Prot database. The software can be freely downloaded at http://soft.synu.edu.cn/upload/msy.rar.
url http://europepmc.org/articles/PMC3374840?pdf=render
work_keys_str_mv AT suyumei multilabelmultikerneltransferlearningforhumanproteinsubcellularlocalization
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