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Results: 1 to 20 of 161

1.

HGVbaseG2P: a central genetic association database.

Thorisson GA, Lancaster O, Free RC, Hastings RK, Sarmah P, Dash D, Brahmachari SK, Brookes AJ.

Nucleic Acids Res. 2009 Jan;37(Database issue):D797-802. doi: 10.1093/nar/gkn748. Epub 2008 Oct 23.

PMID:
18948288
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

[Genome-wide association study on complex diseases: genetic statistical issues].

Yan WL.

Yi Chuan. 2008 May;30(5):543-9. Review. Chinese.

PMID:
18487142
[PubMed - indexed for MEDLINE]
3.

Gevab: a prototype genome variation analysis browsing server.

Kim WY, Kim SY, Kim TH, Ahn SM, Byun HN, Kim D, Kim DS, Lee YS, Ghang H, Park D, Kim BC, Kim C, Lee S, Kim SJ, Bhak J.

BMC Bioinformatics. 2009 Dec 3;10 Suppl 15:S3. doi: 10.1186/1471-2105-10-S15-S3.

PMID:
19958513
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Annotated chromosome maps for renal disease.

McKnight AJ, O'Donoghue D, Peter Maxwell A.

Hum Mutat. 2009 Mar;30(3):314-20. doi: 10.1002/humu.20885.

PMID:
19085929
[PubMed - indexed for MEDLINE]
5.

HGVbase: a curated resource describing human DNA variation and phenotype relationships.

Fredman D, Munns G, Rios D, Sjöholm F, Siegfried M, Lenhard B, Lehväslaiho H, Brookes AJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D516-9.

PMID:
14681471
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays.

Yeung JM, Sham PC, Chan AS, Cherny SS.

BMC Genomics. 2008 Dec 31;9:636. doi: 10.1186/1471-2164-9-636.

PMID:
19117518
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Exploring phenotypic data at the rat genome database.

Twigger SN, S Smith J, Zuniga-Meyer A, Bromberg SK.

Curr Protoc Bioinformatics. 2006 Jul;Chapter 1:Unit 1.14. doi: 10.1002/0471250953.bi0114s14.

PMID:
18428755
[PubMed - indexed for MEDLINE]
8.

"GenotypeColour": colour visualisation of SNPs and CNVs.

Barlati S, Chiesa S, Magri C.

BMC Bioinformatics. 2009 Feb 4;10:49. doi: 10.1186/1471-2105-10-49.

PMID:
19193232
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Management, presentation and interpretation of genome scans using GSCANDB.

Taylor M, Valdar W, Kumar A, Flint J, Mott R.

Bioinformatics. 2007 Jun 15;23(12):1545-9. Epub 2007 Mar 30.

PMID:
17400728
[PubMed - indexed for MEDLINE]
Free Article
10.

The PharmGKB: integration, aggregation, and annotation of pharmacogenomic data and knowledge.

Hodge AE, Altman RB, Klein TE.

Clin Pharmacol Ther. 2007 Jan;81(1):21-4.

PMID:
17185992
[PubMed - indexed for MEDLINE]
11.

The Mouse Genome Database genotypes::phenotypes.

Blake JA, Bult CJ, Eppig JT, Kadin JA, Richardson JE; Mouse Genome Database Group.

Nucleic Acids Res. 2009 Jan;37(Database issue):D712-9. doi: 10.1093/nar/gkn886. Epub 2008 Nov 3.

PMID:
18981050
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

PROPHECY--a database for high-resolution phenomics.

Fernandez-Ricaud L, Warringer J, Ericson E, Pylvänäinen I, Kemp GJ, Nerman O, Blomberg A.

Nucleic Acids Res. 2005 Jan 1;33(Database issue):D369-73.

PMID:
15608218
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genome-wide association database developed in the Japanese Integrated Database Project.

Koike A, Nishida N, Inoue I, Tsuji S, Tokunaga K.

J Hum Genet. 2009 Sep;54(9):543-6. doi: 10.1038/jhg.2009.68. Epub 2009 Jul 24.

PMID:
19629137
[PubMed - indexed for MEDLINE]
14.

SNP@Evolution: a hierarchical database of positive selection on the human genome.

Cheng F, Chen W, Richards E, Deng L, Zeng C.

BMC Evol Biol. 2009 Sep 5;9:221. doi: 10.1186/1471-2148-9-221.

PMID:
19732458
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The YH database: the first Asian diploid genome database.

Li G, Ma L, Song C, Yang Z, Wang X, Huang H, Li Y, Li R, Zhang X, Yang H, Wang J, Wang J.

Nucleic Acids Res. 2009 Jan;37(Database issue):D1025-8. doi: 10.1093/nar/gkn966.

PMID:
19073702
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

GPCR NaVa database: natural variants in human G protein-coupled receptors.

Kazius J, Wurdinger K, van Iterson M, Kok J, Bäck T, Ijzerman AP.

Hum Mutat. 2008 Jan;29(1):39-44.

PMID:
17924574
[PubMed - indexed for MEDLINE]
17.

Evoker: a visualization tool for genotype intensity data.

Morris JA, Randall JC, Maller JB, Barrett JC.

Bioinformatics. 2010 Jul 15;26(14):1786-7. doi: 10.1093/bioinformatics/btq280. Epub 2010 May 27.

PMID:
20507892
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software.

Zaimidou S, van Baal S, Smith TD, Mitropoulos K, Ljujic M, Radojkovic D, Cotton RG, Patrinos GP.

Hum Mutat. 2009 Mar;30(3):308-13. doi: 10.1002/humu.20857.

PMID:
19021233
[PubMed - indexed for MEDLINE]
19.

Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management.

Muñiz-Fernandez F, Carreño-Torres A, Morcillo-Suarez C, Navarro A.

Bioinformatics. 2011 Jul 1;27(13):1871-2. doi: 10.1093/bioinformatics/btr301. Epub 2011 May 17.

PMID:
21586520
[PubMed - indexed for MEDLINE]
Free Article
20.

PROPHECY--a yeast phenome database, update 2006.

Fernandez-Ricaud L, Warringer J, Ericson E, Glaab K, Davidsson P, Nilsson F, Kemp GJ, Nerman O, Blomberg A.

Nucleic Acids Res. 2007 Jan;35(Database issue):D463-7. Epub 2006 Dec 5.

PMID:
17148481
[PubMed - indexed for MEDLINE]
Free PMC Article

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