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NBDC Human Database

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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 hum0147

  • hum0147-v3

    2023-05-08
    Datasets added in this release
    Release note
    RNA extracted from tumor-infiltrating T cell fractions were used for bulk RNA-seq analysis.

  • hum0147-v2

    2022-02-18
    Datasets added in this release
    Release note
    RNA extracted from T cells of peripheral blood mononuclear cells from a healthy donor and tumor-infiltrating T cells from cancer patients were used for single cell RNA-seq analysis. RNA extracted from T cell fractions of peripheral blood mononuclear cells and tumor-infiltrating T cell fractions were used for bulk RNA-seq analysis.

  • hum0147-v1

    2020-05-25
    Datasets added in this release
    Release note
    DNA/RNA extracted from 5 fractions from peripheral blood cells of healthy individuals (Fr1: naive Treg, Fr2: effector Treg, Fr3: Foxp3+ effector conventional T cells, Fr5: effector conventional T cells, Fr6: naive T cells) were used for RNA-seq, ChIP-seq, PBAT-seq, and ATAC-seq analyses.