MGeND: an integrated database for Japanese clinical and genomic information.
Ontology highlight
ABSTRACT:
SUBMITTER: Kamada M
PROVIDER: S-EPMC6897987 | biostudies-literature | 2019
REPOSITORIES: biostudies-literature
Publications
MGeND: an integrated database for Japanese clinical and genomic information.
Kamada Mayumi M Nakatsui Masahiko M Kojima Ryosuke R Nohara Sachio S Uchino Eiichiro E Tanishima Shigeki S Sugiyama Masaya M Kosaki Kenjiro K Tokunaga Katsushi K Mizokami Masashi M Okuno Yasushi Y
Human genome variation 20191206
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 ...[more]
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