MGeND: an integrated database for Japanese clinical and genomic information.
Genetic databases
Genetic variation
Journal
Human genome variation
ISSN: 2054-345X
Titre abrégé: Hum Genome Var
Pays: England
ID NLM: 101652445
Informations de publication
Date de publication:
2019
2019
Historique:
received:
08
04
2019
revised:
29
10
2019
accepted:
31
10
2019
entrez:
17
12
2019
pubmed:
17
12
2019
medline:
17
12
2019
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 31839973
doi: 10.1038/s41439-019-0084-4
pii: 84
pmc: PMC6897987
doi:
Types de publication
Journal Article
Langues
eng
Pagination
53Informations de copyright
© The Author(s) 2019.
Déclaration de conflit d'intérêts
Conflict of interestThe authors declare that they have no conflict of interest.
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