a database of SNPs with high population differentiation for HapMap3 (original) (raw)

Title

FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3

Authors

Shiwei Duan1, Wei Zhang1, Nancy Jean Cox1, 2 and Mary Eileen Dolan1, 3, 4, *

Affiliation

1Section of Hematology/Oncology, Department of Medicine; 2Department of Human Genetics; 3Committee on Clinical Pharmacology and Pharmacogenomics; 4Cancer Research Center, The University of Chicago, IL 60637, USA

Email

edolan@medicine.bsd.uchicago.edu; Corresponding author

Phone

773 702 4441

Fax

773 702 0963

Article Type

Database

Date

received September 16, 2008; revised October 10; accepted October 15, 2008; published November 09, 2008

Abstract

The International HapMap Project has recently made available genotypes and frequency data for phase 3 (NCBI build 36, dbSNP b129) of the HapMap providing an enriched genotype dataset for approximately 1.6 million single nucleotide polymorphisms (SNPs) from 1,115 individuals with ancestry from parts of Africa, Asia, Europe, North America and Mexico. In the present study, we aim to facilitate pharmacogenetics studies by providing a database of SNPs with high population differentiation through a genomewide test on allele frequency variation among 11 HapMap3 samples. Common SNPs with minor allele frequency greater than 5% from each of 11 HapMap3 samples were included in the present analysis. The population differentiation is measured in terms of fixation index (Fst), and the SNPs with Fst values over 0.5 were defined as highly differentiated SNPs. Our tests were carried out between all pairs of the 11 HapMap3 samples or among subgroups with the same continental ancestries. Altogether we carried out 64 genomewide Fst tests and identified 28,215 highly differentiated SNPs for 49 different combinations of HapMap3 samples in the current database.

Keywords

database; HapMap3; SNP; population differentiation; Fst; human genome

Availability

http://FstSNP-hapmap3.googlecode.com/

Citation

Duan et al., Bioinformation 3(3): 139-141 (2008)

Edited by

P. Kangueane

ISSN

0973-2063

Publisher

Biomedical Informatics

License

This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.