Literature DB >> 10592274

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

K H Cheung1, M V Osier, J R Kidd, A J Pakstis, P L Miller, K K Kidd.   

Abstract

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.

Mesh:

Year:  2000        PMID: 10592274      PMCID: PMC102486          DOI: 10.1093/nar/28.1.361

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  7 in total

1.  A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

Authors:  S A Tishkoff; A Goldman; F Calafell; W C Speed; A S Deinard; B Bonne-Tamir; J R Kidd; A J Pakstis; T Jenkins; K K Kidd
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

2.  PhenoDB: an integrated client/server database for linkage and population genetics.

Authors:  K H Cheung; P Nadkarni; S Silverstein; J R Kidd; A J Pakstis; P Miller; K K Kidd
Journal:  Comput Biomed Res       Date:  1996-08

3.  A DNA polymorphism discovery resource for research on human genetic variation.

Authors:  F S Collins; L D Brooks; A Chakravarti
Journal:  Genome Res       Date:  1998-12       Impact factor: 9.043

4.  Variations on a theme: cataloging human DNA sequence variation.

Authors:  F S Collins; M S Guyer; A Charkravarti
Journal:  Science       Date:  1997-11-28       Impact factor: 47.728

5.  HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

Authors:  M E Hawley; K K Kidd
Journal:  J Hered       Date:  1995 Sep-Oct       Impact factor: 2.645

6.  Global patterns of linkage disequilibrium at the CD4 locus and modern human origins.

Authors:  S A Tishkoff; E Dietzsch; W Speed; A J Pakstis; J R Kidd; K Cheung; B Bonné-Tamir; A S Santachiara-Benerecetti; P Moral; M Krings
Journal:  Science       Date:  1996-03-08       Impact factor: 47.728

7.  Global variation of a 40-bp VNTR in the 3'-untranslated region of the dopamine transporter gene (SLC6A3).

Authors:  A M Kang; M A Palmatier; K K Kidd
Journal:  Biol Psychiatry       Date:  1999-07-15       Impact factor: 13.382

  7 in total
  29 in total

1.  ALFRED: an allele frequency database for diverse populations and DNA polymorphisms--an update.

Authors:  M V Osier; K H Cheung; J R Kidd; A J Pakstis; P L Miller; K K Kidd
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

2.  rSNP_Guide, a database system for analysis of transcription factor binding to target sequences: application to SNPs and site-directed mutations.

Authors:  J V Ponomarenko; T I Merkulova; G V Vasiliev; Z B Levashova; G V Orlova; S V Lavryushev; O N Fokin; M P Ponomarenko; A S Frolov; A Sarai
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

3.  A step in another direction: looking for maternal genetic and environmental effects on racial differences in birth weight.

Authors:  E J Van Den Oord; D C Rowe
Journal:  Demography       Date:  2001-11

4.  Opportunities at the intersection of bioinformatics and health informatics: a case study.

Authors:  P L Miller
Journal:  J Am Med Inform Assoc       Date:  2000 Sep-Oct       Impact factor: 4.497

5.  rSNP_Guide, a database system for analysis of transcription factor binding to DNA with variations: application to genome annotation.

Authors:  Julia V Ponomarenko; Tatyana I Merkulova; Galina V Orlova; Oleg N Fokin; Elena V Gorshkova; Anatoly S Frolov; Vadim P Valuev; Mikhail P Ponomarenko
Journal:  Nucleic Acids Res       Date:  2003-01-01       Impact factor: 16.971

6.  Linkage analysis of a complex disease through use of admixed populations.

Authors:  Xiaofeng Zhu; Richard S Cooper; Robert C Elston
Journal:  Am J Hum Genet       Date:  2004-05-06       Impact factor: 11.025

7.  Estimating effective population size or mutation rate with microsatellites.

Authors:  Hongyan Xu; Yun-Xin Fu
Journal:  Genetics       Date:  2004-01       Impact factor: 4.562

8.  Using a pharmacokinetic model to relate an individual's susceptibility to alcohol dependence to genotypes.

Authors:  Laura F Mustavich; Perry Miller; Kenneth K Kidd; Hongyu Zhao
Journal:  Hum Hered       Date:  2010-08-12       Impact factor: 0.444

9.  Synopsis and data synthesis of genetic association studies in hypertension for the adrenergic receptor family genes: the CUMAGAS-HYPERT database.

Authors:  Georgios D Kitsios; Elias Zintzaras
Journal:  Am J Hypertens       Date:  2009-12-31       Impact factor: 2.689

10.  Semantic Web-based integration of cancer pathways and allele frequency data.

Authors:  Matthew E Holford; Haseena Rajeevan; Hongyu Zhao; Kenneth K Kidd; Kei-Hoi Cheung
Journal:  Cancer Inform       Date:  2009-01-15
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