ALFRED: an allele frequency database for diverse populations and DNA polymorphisms

We have developed a publicly accessible database (ALFRED, the ALlele FREquency Database) that catalogues allele frequency data for a wide range of population samples and DNA polymorphisms. This database is web-accessible through our laboratory (Kidd Lab) Web site: http://info.med.yale.edu/genetics/kkidd. ALFRED currently contains data on 60 populations and 156 genetic systems including single nucleotide polymorphisms (SNPs), short tandem repeat polymorphisms (STRPs), variable number of tandem repeats (VNTRs) and insertion-deletion polymorphisms. While data are not available for all population-DNA polymorphism combinations, over 2000 allele frequency tables have been entered. Our database is designed (i) to address our specific research requirements as well as broader scientific objectives; (ii) to allow researchers and interested educators to easily navigate and retrieve data of interest to them; and (iii) to integrate links to other related public databases such as dbSNP, GenBank and PubMed.

[1]  K K Kidd,et al.  Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. , 2000, American journal of human genetics.

[2]  K. Kidd,et al.  HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. , 1995, The Journal of heredity.

[3]  M. Cargill Characterization of single-nucleotide polymorphisms in coding regions of human genes , 1999, Nature Genetics.

[4]  K K Kidd,et al.  A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations. , 1998, American journal of human genetics.

[5]  Jonathan Scott Friedlaender,et al.  Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. , 2000, American journal of human genetics.

[6]  S. Tishkoff,et al.  Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins , 1996, Science.

[7]  W. Speed,et al.  Short tandem repeat polymorphism evolution in humans , 1998, European Journal of Human Genetics.

[8]  Francis S. Collins,et al.  Variations on a Theme: Cataloging Human DNA Sequence Variation , 1997, Science.

[9]  Yan P. Yuan,et al.  HGBASE: a database of SNPs and other variations in and around human genes , 2000, Nucleic Acids Res..

[10]  Anthony M. Kang,et al.  Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3) , 1999, Biological Psychiatry.

[11]  Elizabeth M. Smigielski,et al.  dbSNP: a database of single nucleotide polymorphisms , 2000, Nucleic Acids Res..

[12]  P L Miller,et al.  ALFRED: a Web-accessible allele frequency database. , 1999, Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing.

[13]  Perry L. Miller,et al.  ALFRED: an allele frequency database for diverse populations and DNA polymorphisms - an update , 2001, Nucleic Acids Res..

[14]  K K Kidd,et al.  PhenoDB: an integrated client/server database for linkage and population genetics. , 1996, Computers and biomedical research, an international journal.

[15]  J. Witte,et al.  Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations. , 2000, American journal of human genetics.