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Nucleic Acids Research|November 30, 2012
DbVar and DGVa: public archives for genomic structural variationIlkka Lappalainen, John Lopez, Lisa Skipper, et al.Scientific Data|March 15, 2018
Simplifying research access to genomics and health data with Library CardsMoran N Cabili, Knox Carey, Stephanie O M Dyke, et al.F1000Research|February 25, 2017
Integration of EGA secure data access into GalaxyYouri Hoogstrate, Chao Zhang, Alexander Senf, et al.Neuroinformatics|December 15, 2022
Consent Codes: Maintaining Consent in an Ever-expanding Open Science EcosystemStephanie O M Dyke, Kathleen Connor, Victoria Nembaware, et al.Plos Genetics|January 23, 2016
Consent Codes: Upholding Standard Data Use ConditionsStephanie O M Dyke, Anthony A Philippakis, Jordi Rambla De Argila, et al.Cell Genomics|February 23, 2023
Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseasesAlberto Corvò, Leslie Matalonga, Dylan Spalding, et al.Nature Biotechnology|March 22, 2019
Publisher Correction: Federated discovery and sharing of genomic data using BeaconsMarc Fiume, Miroslav Cupak, Stephen Keenan, et al.Cell Genomics|November 25, 2021
GA4GH Passport standard for digital identity and access permissionsCraig Voisin, Mikael Linden, Stephanie O M Dyke, et al.F1000Research|November 11, 2017
Systematically linking tranSMART, Galaxy and EGA for reusing human translational research dataChao Zhang, Jochem Bijlard, Christine Staiger, et al.European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.Pageof 2