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Low frequency genetic variation may determine complex diseases

Low frequency genetic variation may determine complex diseases
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摘要 In an international project jointly funded by NSFC,researchers in BGI-Shenzhen,China,together with international collaborators from UC Berkeley,University of Copenhagen and some other European institutions conducted research on the re-sequencing and analysis of 200 human exomes,established the largest data set for human exomes published so far and revealed an excess of low frequency deleterious nonsynonymous genetic mutations.Their findings were reported in a paper in Nature Genetics on October 4,2010. In an international project jointly funded by NSFC,researchers in BGI-Shenzhen,China,together with international collaborators from UC Berkeley,University of Copenhagen and some other European institutions conducted research on the re-sequencing and analysis of 200 human exomes,established the largest data set for human exomes published so far and revealed an excess of low frequency deleterious nonsynonymous genetic mutations.Their findings were reported in a paper in Nature Genetics on October 4,2010.
出处 《Science Foundation in China》 CAS 2010年第2期41-41,共1页 中国科学基金(英文版)
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