A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization
A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization
In the absence of a comprehensive experimentally derived mitochondrial proteome, several bioinformatic approaches have been developed to aid the identification of novel mitochondrial disease genes within mapped nuclear genetic loci. Often, many classifiers are combined to increase the sensitivity and specificity of the predictions. Here we show that the greatest sensitivity and specificity are obtained by using a combination of seven carefully selected classifiers. We also show that increasing the number of independent prediction methods can paradoxically decrease the accuracy of predicting mitochondrial localization. This approach will help to accelerate the identification of new mitochondrial disease genes by providing a principled way for the selection for combination of appropriate prediction methods of mitochondrial localization of proteins.
mitochondria, proteome, bioinformatics, oxidative phosphorylation, mitochondrial disease
444-449
Lythgow, Kieren T.
3aeb00d0-0d35-4648-a215-3bafc85205af
Hudson, Gavin
cbad491d-cc7f-4bea-b214-b6752151fc13
Andras, Peter
e4f60324-9221-4e9a-b3d7-b9541eeb8802
Chinnery, Patrick F
87789d1a-5265-4815-9f11-194ed9b4ad94
May 2011
Lythgow, Kieren T.
3aeb00d0-0d35-4648-a215-3bafc85205af
Hudson, Gavin
cbad491d-cc7f-4bea-b214-b6752151fc13
Andras, Peter
e4f60324-9221-4e9a-b3d7-b9541eeb8802
Chinnery, Patrick F
87789d1a-5265-4815-9f11-194ed9b4ad94
Lythgow, Kieren T., Hudson, Gavin, Andras, Peter and Chinnery, Patrick F
(2011)
A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization.
Mitochondrion, 11 (3), .
(doi:10.1016/j.mito.2010.12.016).
(PMID:21195798)
Abstract
In the absence of a comprehensive experimentally derived mitochondrial proteome, several bioinformatic approaches have been developed to aid the identification of novel mitochondrial disease genes within mapped nuclear genetic loci. Often, many classifiers are combined to increase the sensitivity and specificity of the predictions. Here we show that the greatest sensitivity and specificity are obtained by using a combination of seven carefully selected classifiers. We also show that increasing the number of independent prediction methods can paradoxically decrease the accuracy of predicting mitochondrial localization. This approach will help to accelerate the identification of new mitochondrial disease genes by providing a principled way for the selection for combination of appropriate prediction methods of mitochondrial localization of proteins.
This record has no associated files available for download.
More information
Published date: May 2011
Keywords:
mitochondria, proteome, bioinformatics, oxidative phosphorylation, mitochondrial disease
Identifiers
Local EPrints ID: 192203
URI: http://eprints.soton.ac.uk/id/eprint/192203
ISSN: 1567-7249
PURE UUID: 9eee8f89-bb9e-4b35-9f30-63015aa36878
Catalogue record
Date deposited: 30 Jun 2011 12:42
Last modified: 14 Mar 2024 03:49
Export record
Altmetrics
Contributors
Author:
Kieren T. Lythgow
Author:
Gavin Hudson
Author:
Peter Andras
Author:
Patrick F Chinnery
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics