Cargando…
A fast and high performance multiple data integration algorithm for identifying human disease genes
BACKGROUND: Integrating multiple data sources is indispensable in improving disease gene identification. It is not only due to the fact that disease genes associated with similar genetic diseases tend to lie close with each other in various biological networks, but also due to the fact that gene-dis...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582601/ https://www.ncbi.nlm.nih.gov/pubmed/26399620 http://dx.doi.org/10.1186/1755-8794-8-S3-S2 |
_version_ | 1782391729449598976 |
---|---|
author | Chen, Bolin Li, Min Wang, Jianxin Shang, Xuequn Wu, Fang-Xiang |
author_facet | Chen, Bolin Li, Min Wang, Jianxin Shang, Xuequn Wu, Fang-Xiang |
author_sort | Chen, Bolin |
collection | PubMed |
description | BACKGROUND: Integrating multiple data sources is indispensable in improving disease gene identification. It is not only due to the fact that disease genes associated with similar genetic diseases tend to lie close with each other in various biological networks, but also due to the fact that gene-disease associations are complex. Although various algorithms have been proposed to identify disease genes, their prediction performances and the computational time still should be further improved. RESULTS: In this study, we propose a fast and high performance multiple data integration algorithm for identifying human disease genes. A posterior probability of each candidate gene associated with individual diseases is calculated by using a Bayesian analysis method and a binary logistic regression model. Two prior probability estimation strategies and two feature vector construction methods are developed to test the performance of the proposed algorithm. CONCLUSIONS: The proposed algorithm is not only generated predictions with high AUC scores, but also runs very fast. When only a single PPI network is employed, the AUC score is 0.769 by using F(2 )as feature vectors. The average running time for each leave-one-out experiment is only around 1.5 seconds. When three biological networks are integrated, the AUC score using F(3 )as feature vectors increases to 0.830, and the average running time for each leave-one-out experiment takes only about 12.54 seconds. It is better than many existing algorithms. |
format | Online Article Text |
id | pubmed-4582601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45826012015-09-28 A fast and high performance multiple data integration algorithm for identifying human disease genes Chen, Bolin Li, Min Wang, Jianxin Shang, Xuequn Wu, Fang-Xiang BMC Med Genomics Research BACKGROUND: Integrating multiple data sources is indispensable in improving disease gene identification. It is not only due to the fact that disease genes associated with similar genetic diseases tend to lie close with each other in various biological networks, but also due to the fact that gene-disease associations are complex. Although various algorithms have been proposed to identify disease genes, their prediction performances and the computational time still should be further improved. RESULTS: In this study, we propose a fast and high performance multiple data integration algorithm for identifying human disease genes. A posterior probability of each candidate gene associated with individual diseases is calculated by using a Bayesian analysis method and a binary logistic regression model. Two prior probability estimation strategies and two feature vector construction methods are developed to test the performance of the proposed algorithm. CONCLUSIONS: The proposed algorithm is not only generated predictions with high AUC scores, but also runs very fast. When only a single PPI network is employed, the AUC score is 0.769 by using F(2 )as feature vectors. The average running time for each leave-one-out experiment is only around 1.5 seconds. When three biological networks are integrated, the AUC score using F(3 )as feature vectors increases to 0.830, and the average running time for each leave-one-out experiment takes only about 12.54 seconds. It is better than many existing algorithms. BioMed Central 2015-09-23 /pmc/articles/PMC4582601/ /pubmed/26399620 http://dx.doi.org/10.1186/1755-8794-8-S3-S2 Text en Copyright © 2015 Chen et al.; http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chen, Bolin Li, Min Wang, Jianxin Shang, Xuequn Wu, Fang-Xiang A fast and high performance multiple data integration algorithm for identifying human disease genes |
title | A fast and high performance multiple data integration algorithm for identifying human disease genes |
title_full | A fast and high performance multiple data integration algorithm for identifying human disease genes |
title_fullStr | A fast and high performance multiple data integration algorithm for identifying human disease genes |
title_full_unstemmed | A fast and high performance multiple data integration algorithm for identifying human disease genes |
title_short | A fast and high performance multiple data integration algorithm for identifying human disease genes |
title_sort | fast and high performance multiple data integration algorithm for identifying human disease genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582601/ https://www.ncbi.nlm.nih.gov/pubmed/26399620 http://dx.doi.org/10.1186/1755-8794-8-S3-S2 |
work_keys_str_mv | AT chenbolin afastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT limin afastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT wangjianxin afastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT shangxuequn afastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT wufangxiang afastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT chenbolin fastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT limin fastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT wangjianxin fastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT shangxuequn fastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes AT wufangxiang fastandhighperformancemultipledataintegrationalgorithmforidentifyinghumandiseasegenes |