The European Genome-phenome Archive of Human Data Consented for Biomedical Research

Zilbauer M, Rayner T, Clark C, Coffey A, Joyce C, Palta P . Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions. Blood. 2013; 122(25):e52-60. PMC: 3862273. DOI: 10.1182/blood-2013-05-503201. View

Muddyman D, Smee C, Griffin H, Kaye J . Implementing a successful data-management framework: the UK10K managed access model. Genome Med. 2013; 5(11):100. PMC: 3978569. DOI: 10.1186/gm504. View

Trynka G, Hunt K, Bockett N, Romanos J, Mistry V, Szperl A . Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet. 2011; 43(12):1193-201. PMC: 3242065. DOI: 10.1038/ng.998. View

Flicek P, Amode M, Barrell D, Beal K, Billis K, Brent S . Ensembl 2014. Nucleic Acids Res. 2013; 42(Database issue):D749-55. PMC: 3964975. DOI: 10.1093/nar/gkt1196. View

Sato Y, Yoshizato T, Shiraishi Y, Maekawa S, Okuno Y, Kamura T . Integrated molecular analysis of clear-cell renal cell carcinoma. Nat Genet. 2013; 45(8):860-7. DOI: 10.1038/ng.2699. View

Gostev M, Faulconbridge A, Brandizi M, Fernandez-Banet J, Sarkans U, Brazma A . The BioSample Database (BioSD) at the European Bioinformatics Institute. Nucleic Acids Res. 2011; 40(Database issue):D64-70. PMC: 3245134. DOI: 10.1093/nar/gkr937. View

Pakseresht N, Alako B, Amid C, Cerdeno-Tarraga A, Cleland I, Gibson R . Assembly information services in the European Nucleotide Archive. Nucleic Acids Res. 2013; 42(Database issue):D38-43. PMC: 3965037. DOI: 10.1093/nar/gkt1082. View

Welter D, MacArthur J, Morales J, Burdett T, Hall P, Junkins H . The NHGRI GWAS Catalog, a curated resource of SNP-trait associations. Nucleic Acids Res. 2013; 42(Database issue):D1001-6. PMC: 3965119. DOI: 10.1093/nar/gkt1229. View

Adams D, Altucci L, Antonarakis S, Ballesteros J, Beck S, Bird A . BLUEPRINT to decode the epigenetic signature written in blood. Nat Biotechnol. 2012; 30(3):224-6. DOI: 10.1038/nbt.2153. View

10.

Wiegand K, Shah S, Al-Agha O, Zhao Y, Tse K, Zeng T . ARID1A mutations in endometriosis-associated ovarian carcinomas. N Engl J Med. 2010; 363(16):1532-43. PMC: 2976679. DOI: 10.1056/NEJMoa1008433. View

11.

Surakka I, Kristiansson K, Anttila V, Inouye M, Barnes C, Moutsianas L . Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. Genome Res. 2010; 20(10):1344-51. PMC: 2945183. DOI: 10.1101/gr.106534.110. View

12.

Mailman M, Feolo M, Jin Y, Kimura M, Tryka K, Bagoutdinov R . The NCBI dbGaP database of genotypes and phenotypes. Nat Genet. 2007; 39(10):1181-6. PMC: 2031016. DOI: 10.1038/ng1007-1181. View

13.

Vizcaino J, Cote R, Csordas A, Dianes J, Fabregat A, Foster J . The PRoteomics IDEntifications (PRIDE) database and associated tools: status in 2013. Nucleic Acids Res. 2012; 41(Database issue):D1063-9. PMC: 3531176. DOI: 10.1093/nar/gks1262. View

14.

Kulis M, Heath S, Bibikova M, Queiros A, Navarro A, Clot G . Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia. Nat Genet. 2012; 44(11):1236-42. DOI: 10.1038/ng.2443. View

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Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis G . Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet. 2012; 44(8):955-9. PMC: 3696580. DOI: 10.1038/ng.2354. View

16.

Artez A, Bernabe R, Eerola I, Hemsley F, Jennings J, Kerr D . International network of cancer genome projects. Nature. 2010; 464(7291):993-8. PMC: 2902243. DOI: 10.1038/nature08987. View

17.

Berndt S, Gustafsson S, Magi R, Ganna A, Wheeler E, Feitosa M . Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet. 2013; 45(5):501-12. PMC: 3973018. DOI: 10.1038/ng.2606. View

18.

Ban M, Goris A, Lorentzen A, Baker A, Mihalova T, Ingram G . Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. Eur J Hum Genet. 2009; 17(10):1309-13. PMC: 2782567. DOI: 10.1038/ejhg.2009.41. View

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Firth H, Wright C . The Deciphering Developmental Disorders (DDD) study. Dev Med Child Neurol. 2011; 53(8):702-3. DOI: 10.1111/j.1469-8749.2011.04032.x. View

20.

Kaye J . The tension between data sharing and the protection of privacy in genomics research. Annu Rev Genomics Hum Genet. 2012; 13:415-31. PMC: 4337968. DOI: 10.1146/annurev-genom-082410-101454. View