MGeND: an integrated database for Japanese clinical and genomic information

Mayumi Kamada, Masahiko Nakatsui, Ryosuke Kojima, Sachio Nohara, Eiichiro Uchino, Shigeki Tanishima, Masaya Sugiyama, Kenjiro Kosaki, Katsushi Tokunaga, Masashi Mizokami, Yasushi Okuno

研究成果: Article査読

3 被引用数 (Scopus)

抄録

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.

本文言語English
論文番号53
ジャーナルHuman Genome Variation
6
1
DOI
出版ステータスPublished - 2019 12月 1

ASJC Scopus subject areas

  • 生化学
  • 分子生物学
  • 遺伝学

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