Please use this identifier to cite or link to this item:
|Title:||Natural positive selection and north-south genetic diversity in East Asia|
|Authors:||Suo, C. |
linkage disequilibrium variation
|Citation:||Suo, C., Xu, H., Khor, C.-C., Ong, R.T.H., Sim, X., Chen, J., Tay, W.-T., Sim, K.-S., Zeng, Y.-X., Zhang, X., Liu, J., Tai, E.-S., Wong, T.-Y., Chia, K.-S., Teo, Y.-Y. (2012-01). Natural positive selection and north-south genetic diversity in East Asia. European Journal of Human Genetics 20 (1) : 102-110. ScholarBank@NUS Repository. https://doi.org/10.1038/ejhg.2011.139|
|Abstract:||Recent reports have identified a north-south cline in genetic variation in East and South-East Asia, but these studies have not formally explored the basis of these clinical differences. Understanding the origins of these variations may provide valuable insights in tracking down the functional variants in genomic regions identified by genetic association studies. Here we investigate the genetic basis of these differences with genome-wide data from the HapMap, the Human Genome Diversity Project and the Singapore Genome Variation Project. We implemented four bioinformatic measures to discover genomic regions that are considerably differentiated either between two Han Chinese populations in the north and south of China, or across 22 populations in East and South-East Asia. These measures prioritized genomic stretches with: (i) regional differences in the allelic spectrum for SNPs common to the two Han Chinese populations; (ii) differential evidence of positive selection between the two populations as quantified by integrated haplotype score (iHS) and cross-population extended haplotype homozygosity (XP-EHH); (iii) significant correlation between allele frequencies and geographical latitudes of the 22 populations. We also explored the extent of linkage disequilibrium variations in these regions, which is important in combining genetic association studies from North and South Chinese. Two of the regions that emerged are found in HLA class I and II, suggesting that the HLA imputation panel from the HapMap may not be directly applicable to every Chinese sample. This has important implications to autoimmune studies that plan to impute the classical HLA alleles to fine map the SNP association signals. © 2012 Macmillan Publishers Limited All rights reserved.|
|Source Title:||European Journal of Human Genetics|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 18, 2018
WEB OF SCIENCETM
checked on Jun 4, 2018
checked on Jul 6, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.