Literature DB >> 10902212

ALFRED: a Web-accessible allele frequency database.

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

Abstract

We present a Web-accessible database (ALFRED) that allows public access to gene frequency data for a diverse set of population samples and genetic systems. The data in ALFRED are modeled based on the experience and needs of a single laboratory, but with the expectation that the database will meet the needs of a much broader scientific community that needs population-specific gene frequency estimates. Our database currently contains data on more than 40 populations representing most major regions of the world and data on more than 150 genetic systems including SNPs, STRPs, and insertion-deletion polymorphisms. While data are not available for all population-genetic system combinations, over 2000 allele frequency tables already exist. In this paper, we enumerate the broad needs in the scientific domain, describe their significance, and describe how we have designed the database to meet those needs. We compare our database with dbSNP, the NCBI database that has a broader but overlapping purpose.

Mesh:

Year:  2000        PMID: 10902212     DOI: 10.1142/9789814447331_0062

Source DB:  PubMed          Journal:  Pac Symp Biocomput        ISSN: 2335-6928


  6 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.  Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.

Authors:  Robert Brown; Hane Lee; Ascia Eskin; Gleb Kichaev; Kirk E Lohmueller; Bruno Reversade; Stanley F Nelson; Bogdan Pasaniuc
Journal:  Eur J Hum Genet       Date:  2015-04-22       Impact factor: 4.246

3.  Non-replication of an association of Apolipoprotein E2 with sinistrality.

Authors:  Brian J Piper; Alia L Yasen; Amy E Taylor; Jonatan R Ruiz; J William Gaynor; Catherine A Dayger; Marcela Gonzalez-Gross; Oh D Kwon; Lars-Göran Nilsson; Ian N M Day; Jacob Raber; Jeremy K Miller
Journal:  Laterality       Date:  2012-06-21

4.  Extreme individual marker F(ST )values do not imply population-specific selection in humans: the NRG1 example.

Authors:  Michelle Gardner; Scott Williamson; Ferran Casals; Elena Bosch; Arcadi Navarro; Francesc Calafell; Jaume Bertranpetit; David Comas
Journal:  Hum Genet       Date:  2007-04-25       Impact factor: 5.881

5.  Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio test.

Authors:  Wonkuk Kim; Derek Gordon; Jonathan Sebat; Kenny Q Ye; Stephen J Finch
Journal:  PLoS One       Date:  2008-10-22       Impact factor: 3.240

6.  Molecular phylogeography of a human autosomal skin color locus under natural selection.

Authors:  Victor A Canfield; Arthur Berg; Steven Peckins; Steven M Wentzel; Khai Chung Ang; Stephen Oppenheimer; Keith C Cheng
Journal:  G3 (Bethesda)       Date:  2013-11-06       Impact factor: 3.154

  6 in total

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