MGeND: an integrated database for Japanese clinical and genomic information

To promote the implementation of genomic medicine, we developed an integrated database, the Medical Genomics Japan Variant Database (MGeND). In its first release, MGeND provides data regarding genomic variations in Japanese individuals, collected by research groups in five disease fields. These vari...

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Detalles Bibliográficos
Autores principales: Kamada, Mayumi, Nakatsui, Masahiko, Kojima, Ryosuke, Nohara, Sachio, Uchino, Eiichiro, Tanishima, Shigeki, Sugiyama, Masaya, Kosaki, Kenjiro, Tokunaga, Katsushi, Mizokami, Masashi, Okuno, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Software Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897987/
https://www.ncbi.nlm.nih.gov/pubmed/31839973
http://dx.doi.org/10.1038/s41439-019-0084-4
Descripción
Sumario:To promote the implementation of genomic medicine, we developed an integrated database, the Medical Genomics Japan Variant Database (MGeND). In its first release, MGeND provides data regarding genomic variations in Japanese individuals, collected by research groups in five disease fields. These variations consist of curated SNV/INDEL variants and susceptibility variants for diseases established by genome-wide association study analysis. Furthermore, we recorded the frequencies of HLA alleles in infectious disease populations.

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