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Musings on genome medicine: the value of family history
Will the routine availability of genome sequence information on individuals render family history information obsolete? I argue that it will not, both because the taking of a family history has other uses for the health professional, and because genome sequence data on their own omit the effects of...
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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/PMC2768961/ https://www.ncbi.nlm.nih.gov/pubmed/19664195 http://dx.doi.org/10.1186/gm75 |
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author | Clarke, Angus John |
author_facet | Clarke, Angus John |
author_sort | Clarke, Angus John |
collection | PubMed |
description | Will the routine availability of genome sequence information on individuals render family history information obsolete? I argue that it will not, both because the taking of a family history has other uses for the health professional, and because genome sequence data on their own omit the effects of numerous factors important for modifying risks of disease. These include information derived from factors downstream of genetic variants and from upstream epigenetic effects. Further difficulties arise with uncertainties relating to gene-gene and gene-environment interactions, which may take decades to resolve if their resolution is even possible. |
format | Text |
id | pubmed-2768961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27689612010-08-03 Musings on genome medicine: the value of family history Clarke, Angus John Genome Med Musings Will the routine availability of genome sequence information on individuals render family history information obsolete? I argue that it will not, both because the taking of a family history has other uses for the health professional, and because genome sequence data on their own omit the effects of numerous factors important for modifying risks of disease. These include information derived from factors downstream of genetic variants and from upstream epigenetic effects. Further difficulties arise with uncertainties relating to gene-gene and gene-environment interactions, which may take decades to resolve if their resolution is even possible. BioMed Central 2009-08-03 /pmc/articles/PMC2768961/ /pubmed/19664195 http://dx.doi.org/10.1186/gm75 Text en Copyright ©2009 BioMed Central Ltd |
spellingShingle | Musings Clarke, Angus John Musings on genome medicine: the value of family history |
title | Musings on genome medicine: the value of family history |
title_full | Musings on genome medicine: the value of family history |
title_fullStr | Musings on genome medicine: the value of family history |
title_full_unstemmed | Musings on genome medicine: the value of family history |
title_short | Musings on genome medicine: the value of family history |
title_sort | musings on genome medicine: the value of family history |
topic | Musings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768961/ https://www.ncbi.nlm.nih.gov/pubmed/19664195 http://dx.doi.org/10.1186/gm75 |
work_keys_str_mv | AT clarkeangusjohn musingsongenomemedicinethevalueoffamilyhistory |