Cargando…
Unsupervised Outlier Profile Analysis
In much of the analysis of high-throughput genomic data, “interesting” genes have been selected based on assessment of differential expression between two groups or generalizations thereof. Most of the literature focuses on changes in mean expression or the entire distribution. In this article, we e...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218656/ https://www.ncbi.nlm.nih.gov/pubmed/25452686 http://dx.doi.org/10.4137/CIN.S13969 |
_version_ | 1782342453098971136 |
---|---|
author | Ghosh, Debashis Li, Song |
author_facet | Ghosh, Debashis Li, Song |
author_sort | Ghosh, Debashis |
collection | PubMed |
description | In much of the analysis of high-throughput genomic data, “interesting” genes have been selected based on assessment of differential expression between two groups or generalizations thereof. Most of the literature focuses on changes in mean expression or the entire distribution. In this article, we explore the use of C(α) tests, which have been applied in other genomic data settings. Their use for the outlier expression problem, in particular with continuous data, is problematic but nevertheless motivates new statistics that give an unsupervised analog to previously developed outlier profile analysis approaches. Some simulation studies are used to evaluate the proposal. A bivariate extension is described that can accommodate data from two platforms on matched samples. The proposed methods are applied to data from a prostate cancer study. |
format | Online Article Text |
id | pubmed-4218656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-42186562014-12-01 Unsupervised Outlier Profile Analysis Ghosh, Debashis Li, Song Cancer Inform Review In much of the analysis of high-throughput genomic data, “interesting” genes have been selected based on assessment of differential expression between two groups or generalizations thereof. Most of the literature focuses on changes in mean expression or the entire distribution. In this article, we explore the use of C(α) tests, which have been applied in other genomic data settings. Their use for the outlier expression problem, in particular with continuous data, is problematic but nevertheless motivates new statistics that give an unsupervised analog to previously developed outlier profile analysis approaches. Some simulation studies are used to evaluate the proposal. A bivariate extension is described that can accommodate data from two platforms on matched samples. The proposed methods are applied to data from a prostate cancer study. Libertas Academica 2014-10-15 /pmc/articles/PMC4218656/ /pubmed/25452686 http://dx.doi.org/10.4137/CIN.S13969 Text en © 2014 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License. |
spellingShingle | Review Ghosh, Debashis Li, Song Unsupervised Outlier Profile Analysis |
title | Unsupervised Outlier Profile Analysis |
title_full | Unsupervised Outlier Profile Analysis |
title_fullStr | Unsupervised Outlier Profile Analysis |
title_full_unstemmed | Unsupervised Outlier Profile Analysis |
title_short | Unsupervised Outlier Profile Analysis |
title_sort | unsupervised outlier profile analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218656/ https://www.ncbi.nlm.nih.gov/pubmed/25452686 http://dx.doi.org/10.4137/CIN.S13969 |
work_keys_str_mv | AT ghoshdebashis unsupervisedoutlierprofileanalysis AT lisong unsupervisedoutlierprofileanalysis |