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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 hum0005

  • hum0005-v8

    2023-10-02
    Datasets added in this release
    Release note
    1) DNAs extracted from peripheral blood cells of 1410 Japanese non-syndromic hearing loss patients were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    2) DNAs extracted from peripheral blood cells of 1559 Japanese non-syndromic hearing loss patients were used and 63 gene regions (295 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).

  • hum0005-v7

    2021-11-19
    Datasets added in this release
    Release note
    1) DNAs extracted from peripheral blood cells of 3 Japanese non-syndromic hearing loss patients were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    2) DNAs extracted from peripheral blood cells of 11 Japanese non-syndromic hearing loss patients were used and 63 gene regions (295 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton/Ion S5] (Single-end: 200 bp).
    3) DNAs extracted from peripheral blood cells of 1 Japanese non-syndromic hearing loss patients were used and 90 gene regions (568 kb) were targeted to this study. The regions were narrowed down by using of Agilent Sure Select XT and read the sequences by Illumina [HiSeq 2000] (Paired-end: 100 bp).

  • hum0005-v6

    2021-07-30
    Datasets added in this release
    Release note
    1) DNAs extracted from peripheral blood cells of 17 Japanese non-syndromic hearing loss patients (JGAS000191: 1 patient, JGAS000192: 9 patients, JGAS000201: 7 patients) were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    2) DNAs extracted from peripheral blood cells of 39 Japanese non-syndromic hearing loss patients (JGAS000192: 17 patients, JGAS000200: 7 patients, JGAS000201: 15 patients) were used and 63 gene regions (295 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    3) DNAs extracted from peripheral blood cells of 6 Japanese non-syndromic hearing loss patients (JGAS000192: 2 patients, JGAS000201: 4 patients) were used and 90 gene regions (568 kb) were targeted to this study. The regions were narrowed down by using of Agilent Sure Select XT and read the sequences by Illumina [HiSeq 2000] (Paired-end: 100 bp).

  • hum0005-v5

    2019-04-18
    Datasets added in this release
    Release note
    1) DNAs extracted from peripheral blood cells of 37 Japanese non-syndromic hearing loss patients were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    2) DNAs extracted from peripheral blood cells of 2 Japanese non-syndromic hearing loss patients were used and 90 gene regions (568 kb) were targeted to this study. The regions were narrowed down by using of Agilent Sure Select XT and read the sequences by Illumina [HiSeq 2000] (Paired-end: 100 bp).

  • hum0005-v4

    2018-02-13
    Datasets added in this release
    Release note
    1) DNAs extracted from peripheral blood cells of 16 Japanese non-syndromic hearing loss patients were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM/Ion Proton] (Single-end: 200 bp).
    2) DNAs extracted from peripheral blood cells of 3 Japanese non-syndromic hearing loss patients were used and 90 gene regions (568 kb) were targeted to this study. The regions were narrowed down by using of Agilent Sure Select XT and read the sequences by Illumina [HiSeq 2000] (Paired-end: 100 bp).

  • hum0005-v3

    2017-06-19
    Datasets added in this release
    Release note
    DNAs extracted from peripheral blood cells of 19 Japanese non-syndromic hearing loss patients were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM] or [Ion Proton] (Single-end: 200 bp).

  • hum0005-v2

    2017-02-24
    Datasets added in this release
    Release note
    DNAs extracted from peripheral blood cells of 44 Japanese non-syndromic hearing loss patients (JGAS000032: 39 patients, DRA003791: 5 patients) were used and 69 gene regions (354 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit or Ion AmpliSeq Library Kit ver 2.0 and read the sequences by Thermo Fisher Scientific [Ion PGM] or [Ion Proton] (Single-end: 200 bp).

  • hum0005-v1

    2014-01-27
    Datasets added in this release
    Release note
    DNAs extracted from peripheral blood cells of 17 Japanese Usher syndrome patients were used and 9 gene regions (109 kb) were targeted to this study. The regions were narrowed down by using of the Ion AmpliSeq Custom kit and read the sequences by Thermo Fisher Scientific [Ion PGM] (Single-end: 200 bp).