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Integration of a priori gene set information into genome-wide association studies
In genome-wide association studies (GWAS) genetic markers are often ranked to select genes for further pursuit. Especially for moderately associated and interrelated genes, information on genes and pathways may improve the selection. We applied and combined two main approaches for data integration t...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795999/ https://www.ncbi.nlm.nih.gov/pubmed/20018092 http://dx.doi.org/10.1186/1753-6561-3-S7-S95 |
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author | Sohns, Melanie Rosenberger, Albert Bickeböller, Heike |
author_facet | Sohns, Melanie Rosenberger, Albert Bickeböller, Heike |
author_sort | Sohns, Melanie |
collection | PubMed |
description | In genome-wide association studies (GWAS) genetic markers are often ranked to select genes for further pursuit. Especially for moderately associated and interrelated genes, information on genes and pathways may improve the selection. We applied and combined two main approaches for data integration to a GWAS for rheumatoid arthritis, gene set enrichment analysis (GSEA) and hierarchical Bayes prioritization (HBP). Many associated genes are located in the HLA region on 6p21. However, the ranking lists of genes and gene sets differ considerably depending on the chosen approach: HBP changes the ranking only slightly and primarily contains HLA genes in the top 100 gene lists. GSEA includes also many non-HLA genes. |
format | Text |
id | pubmed-2795999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27959992009-12-18 Integration of a priori gene set information into genome-wide association studies Sohns, Melanie Rosenberger, Albert Bickeböller, Heike BMC Proc Proceedings In genome-wide association studies (GWAS) genetic markers are often ranked to select genes for further pursuit. Especially for moderately associated and interrelated genes, information on genes and pathways may improve the selection. We applied and combined two main approaches for data integration to a GWAS for rheumatoid arthritis, gene set enrichment analysis (GSEA) and hierarchical Bayes prioritization (HBP). Many associated genes are located in the HLA region on 6p21. However, the ranking lists of genes and gene sets differ considerably depending on the chosen approach: HBP changes the ranking only slightly and primarily contains HLA genes in the top 100 gene lists. GSEA includes also many non-HLA genes. BioMed Central 2009-12-15 /pmc/articles/PMC2795999/ /pubmed/20018092 http://dx.doi.org/10.1186/1753-6561-3-S7-S95 Text en Copyright ©2009 Sohns et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Sohns, Melanie Rosenberger, Albert Bickeböller, Heike Integration of a priori gene set information into genome-wide association studies |
title | Integration of a priori gene set information into genome-wide association studies |
title_full | Integration of a priori gene set information into genome-wide association studies |
title_fullStr | Integration of a priori gene set information into genome-wide association studies |
title_full_unstemmed | Integration of a priori gene set information into genome-wide association studies |
title_short | Integration of a priori gene set information into genome-wide association studies |
title_sort | integration of a priori gene set information into genome-wide association studies |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795999/ https://www.ncbi.nlm.nih.gov/pubmed/20018092 http://dx.doi.org/10.1186/1753-6561-3-S7-S95 |
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