HGVA specifications

Information


Unique identifier OMICS_18704
Name HGVA
Alternative name Human Genome Variation Archive
Restrictions to use None
Database management system NoSQL
Community driven No
Data access File download, Browse
User data submission Not allowed
Version 1.1.0
Maintained Yes

Maintainers


  • person_outline Ignacio Medina <>
  • person_outline Javier Lopez <>
  • person_outline Joaquin Dopazo <>

Publication for Human Genome Variation Archive

HGVA institution(s)
Genomics England, Charterhouse Square, London, UK; Department of Haematology, University of Cambridge, Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK; HPC Service, UIS, University of Cambridge, Cambridge, UK; Clinical Bioinformatics Area, Fundacion Progreso y Salud (FPS), Hospital Virgen del Rocio, Sevilla, Spain; Functional Genomics Node (INB), FPS, Hospital Virgen del Rocio, Sevilla, Spain; Bioinformatics in Rare Diseases (BiER), Centro de Investigacion Biomedica en Red de Enfermedades Raras (CIBERER), FPS, Hospital Virgen del Rocio, Sevilla, Spain
HGVA funding source(s)
Supported by Spanish Ministry of Economy and Competitiveness [BIO2014-57291-R, in part]; Instituto de Salud Carlos III (ISCIII) Plataforma de Recursos Biomoleculares y Bioinformaticos [PT13/0001/0007]; European Regional Development Funds (ERDF) [EU H2020-INFRADEV-1- 2015-1 ELIXIR-EXCELERATE (ref. 676559)]; National Institute for Health Research (NIHR) England [RG65966].

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