RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases

被引:56
作者
Lochmueller, Hanns [1 ,2 ]
Badowska, Dorota M. [1 ]
Thompson, Rachel [1 ]
Knoers, Nine V. [3 ]
Aartsma-Rus, Annemieke [1 ,4 ]
Gut, Ivo [5 ]
Wood, Libby [1 ]
Harmuth, Tina [6 ]
Durudas, Andre [7 ,8 ]
Graessner, Holm [6 ,9 ]
Schaefer, Franz [10 ]
Riess, Olaf [6 ,9 ]
机构
[1] Newcastle Univ, Inst Med Genet, MRC Ctr Neuromuscular Dis, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Freiburg, Fac Med, Med Ctr, Dept Neuropediat & Muscle Disorders, Freiburg, Germany
[3] Univ Med Ctr Utrecht, Ctr Mol Med, Dept Genet, Utrecht, Netherlands
[4] Leiden Univ, Med Ctr, Leiden, Netherlands
[5] Barcelona Inst Sci & Technol, CNAG CRG, Ctr Genom Regulat, Ctr Nacl Anal Genom, Barcelona, Spain
[6] Univ Tubingen, Dept Med Genet & Appl Genom, Tubingen, Germany
[7] CMAST Bvba, Strateg Collaborat, Munich, Germany
[8] CMAST Bvba, Strateg Collaborat, Temse, Belgium
[9] Univ Tubingen, Ctr Rare Dis, Tubingen, Germany
[10] Heidelberg Univ, Div Pediat Nephrol, Ctr Pediat & Adolescent Med, Heidelberg, Germany
基金
英国医学研究理事会;
关键词
PHENOTYPIC SPECTRUM; NEPHROTIC SYNDROME; STEROID-RESISTANT; UMD-PREDICTOR; GLOMERULOPATHY; MUTATIONS; COHORT; SUBSTITUTION; EXPRESSION; SOFTWARE;
D O I
10.1038/s41431-018-0115-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although individually uncommon, rare diseases (RDs) collectively affect 6-8% of the population. The unmet need of the rare disease community was recognized by the European Commission which in 2012 funded three flagship projects, RD-Connect, NeurOmics, and EURenOmics, to help move the field forward with the ambition of advancing -omics research and data sharing at their core in line with the goals of IRDiRC (International Rare Disease Research Consortium). NeurOmics and EURenOmics generate -omics data and improve diagnosis and therapy in rare renal and neurological diseases, with RD-Connect developing an infrastructure to facilitate the sharing, systematic integration and analysis of these data. Here, we summarize the achievements of these three projects, their impact on the RD community and their vision for the future. We also report from the Joint Outreach Day organized by the three projects on the 3rd of May 2017 in Berlin. The workshop stimulated an open, multi-stakeholder discussion on the challenges of the rare diseases, and highlighted the cross-project cooperation and the common goal: the use of innovative genomic technologies in rare disease research.
引用
收藏
页码:778 / 785
页数:8
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