Databases for neurogenetics: Introduction, overview, and challenges

被引:1
|
作者
Sobrido, Maria-Jesus [1 ,2 ]
Cacheiro, Pilar [3 ]
Carracedo, Angel [2 ,3 ]
Bertram, Lars [4 ]
机构
[1] Clin Hosp Santiago, Fdn Publ Galega Med Xen, SERGAS, Santiago De Compostela 15706, Spain
[2] Inst Hlth Carlos III, Ctr Network Biomed Res Rare Dis CIBERER, Madrid, Spain
[3] Univ Santiago de Compostela, Genom Med Grp, Galicia, Spain
[4] Max Planck Inst Mol Genet, Dept Vertebrate Genom, Neuropsychiat Genet Grp, D-14195 Berlin, Germany
关键词
Neurogenetics; LSDB; databases; HVP; genotype-phenotype; LOCUS-SPECIFIC DATABASES; PHENOTYPE; DISEASE;
D O I
10.1002/humu.22164
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The importance for research and clinical utility of mutation databases, as well as the issues and difficulties entailed in their construction, is discussed within the Human Variome Project. While general principles and standards can apply to most human diseases, some specific questions arise when dealing with the nature of genetic neurological disorders. So far, publically accessible mutation databases exist for only about half of the genes causing neurogenetic disorders; and a considerable work is clearly still needed to optimize their content. The current landscape, main challenges, some potential solutions, and future perspectives on genetic databases for disorders of the nervous system are reviewed in this special issue of Human Mutation on neurogenetics. Hum Mutat 33:13111314, 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1311 / 1314
页数:4
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