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Due to system maintenance, the application system, application review by the Data Access Committee will be unavailable during the following period.
Schedule: October 5th (Mon), 2026, 9:00 - October 7th (Wed), 2026, 15:00 (JST)
We apologize for any inconvenience this may cause and appreciate your understanding.

We are currently receiving a large number of applications for data submission, and the review process is taking longer than usual.We sincerely apologize for the delay and kindly ask for your understanding. When submitting an application, we would greatly appreciate it if you could allow sufficient time for the processing.

Following a change to our organizational structure effective April 1, 2026, this division has been renamed from the "Database Center for Life Science, Joint Support-Center for Data Science Research" to the "Database Division for Life Science (DBCLS), BioData Science Initiative (BSI), National Institute of Genetics (NIG)". Where the former name still appears in the guidelines, please read it as the new name.

Release info for hum0163

  • hum0163-v3

    2023-04-21
    Datasets added in this release
    Release note
    DNAs extracted from peripheral blood cells of bullous pemphigoid patients and B-lymphoblast cells were genotyped by using of Illumina Infinium OmniExpressExome BeadChip and a genome-wide association study was performed (xlsx file).

  • hum0163-v2

    2021-02-09
    Datasets added in this release
    Release note
    Genotype frequencies of NAT2 identified from the targeted capture sequencing (NGS) analysis were provided (csv file).

  • hum0163-v1

    2018-12-14
    Datasets added in this release
    Release note
    DNAs extracted from peripheral blood cells of patients with psychiatric/neurological disorders or cancers were used for the targeted NGS analysis focusing on 100 pharmacogenes and CYP2D6. Allele frequencies of 100 pharmacogenes (1846 variants) and genotype frequencies of CYP2D6 for 990 patients were provided (csv file).
    Libraries were prepared by using of in-house multiplexPCR and read by Illumina [MiSeq] (paired-end: average read length 377 bp).