Format:
Online-Ressource
ISSN:
1469-3178
Content:
The EMBO/EMBL symposium ‘Human Variation: Cause and Consequence’ highlighted advances in understanding the molecular basis of human genetic variation and its myriad implications for biology, human origins and disease. As high‐throughput sequencing allows us to define genetic variation and its functional consequences at genome‐wide resolution for a large number of people, important questions need to be asked about how to use new technologies to maximize the translational relevance of genetic research for society and the individual patient.
Content:
The EMBO/EMBL symposium ‘Human Variation: Cause and Consequence’ highlighted advances in understanding the molecular basis of human genetic variation and its myriad implications for biology, human origins and disease.
In:
volume:11
In:
number:9
In:
year:2010
In:
pages:650-652
In:
extent:3
In:
European Molecular Biology Organization, EMBO reports, Heidelberg : EMBO Press, [200]-, 11, Heft 9 (2010), 650-652 (gesamt 3), 1469-3178
Language:
English
DOI:
10.1038/embor.2010.126
URN:
urn:nbn:de:101:1-2023041415410176016410
URL:
https://doi.org/10.1038/embor.2010.126
URL:
https://nbn-resolving.org/urn:nbn:de:101:1-2023041415410176016410
URL:
https://d-nb.info/1286271541/34
URL:
https://doi.org/10.1038/embor.2010.126