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Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis
The efforts of the Human Genome Project are beginning to provide important findings for human health. Technological advances in the laboratory, particularly in characterizing human genomic variation, have created new approaches for studying the human genome - genome-wide association studies (GWAS)....
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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/PMC2703874/ https://www.ncbi.nlm.nih.gov/pubmed/19566917 http://dx.doi.org/10.1186/gm65 |
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author | Ritchie, Marylyn D |
author_facet | Ritchie, Marylyn D |
author_sort | Ritchie, Marylyn D |
collection | PubMed |
description | The efforts of the Human Genome Project are beginning to provide important findings for human health. Technological advances in the laboratory, particularly in characterizing human genomic variation, have created new approaches for studying the human genome - genome-wide association studies (GWAS). However, current statistical and computational strategies are taking only partial advantage of this wealth of information. In the quest for susceptibility genes for complex diseases in GWAS data, several different analytic strategies are being pursued. In a recent report, Baranzini and colleagues used a pathway- and network-based analysis to explore potentially interesting single locus association signals in a GWAS of multiple sclerosis. This and other pathway-based approaches are likely to continue to emerge in the GWAS literature, as they provide a powerful strategy to detect important modest single-locus effects and gene-gene interaction effects. |
format | Text |
id | pubmed-2703874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27038742010-06-29 Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis Ritchie, Marylyn D Genome Med Minireview The efforts of the Human Genome Project are beginning to provide important findings for human health. Technological advances in the laboratory, particularly in characterizing human genomic variation, have created new approaches for studying the human genome - genome-wide association studies (GWAS). However, current statistical and computational strategies are taking only partial advantage of this wealth of information. In the quest for susceptibility genes for complex diseases in GWAS data, several different analytic strategies are being pursued. In a recent report, Baranzini and colleagues used a pathway- and network-based analysis to explore potentially interesting single locus association signals in a GWAS of multiple sclerosis. This and other pathway-based approaches are likely to continue to emerge in the GWAS literature, as they provide a powerful strategy to detect important modest single-locus effects and gene-gene interaction effects. BioMed Central 2009-06-29 /pmc/articles/PMC2703874/ /pubmed/19566917 http://dx.doi.org/10.1186/gm65 Text en Copyright ©2009 BioMed Central Ltd |
spellingShingle | Minireview Ritchie, Marylyn D Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title | Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title_full | Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title_fullStr | Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title_full_unstemmed | Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title_short | Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
title_sort | using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2703874/ https://www.ncbi.nlm.nih.gov/pubmed/19566917 http://dx.doi.org/10.1186/gm65 |
work_keys_str_mv | AT ritchiemarylynd usingpriorknowledgeandgenomewideassociationtoidentifypathwaysinvolvedinmultiplesclerosis |