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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 hum0216

  • hum0216-v4

    2021-04-13
    Datasets added in this release
    Release note
    DNAs extracted from matched tumor and non-tumor tissues from 7 patients with colorectal cancer were used for the whole exome sequencing (fastq files). DNA libraries were established with a SureSelect Human All Exon Kit v5 and sequenced by Illumina NovaSeq 6000 system (paired-end; 150 bp).

  • hum0216-v3

    2021-03-29
    Datasets added in this release

    No datasets were added.

    Release note
    DNAs extracted from matched tumor and non-tumor tissues from 23 patients with gastric cancers were used for the whole exome sequencing (fastq files). DNA libraries were established with a SureSelect XT Human All Exon system and sequenced by Illumina HiSeq 2500 system (paired-end; 100 bp).

  • hum0216-v2

    2020-09-25
    Datasets added in this release
    Release note
    DNAs extracted from matched tumor and non-tumor tissues from 40 patients with malignancies who received PD-1 blackade therapy were used for the whole exome sequencing (fastq files). DNA libraries were established with a NEBNext Ultra DNA Library Prep Kit and sequenced by Illumina HiSeq 2500 system (paired-end; 120-150 bp).

  • hum0216-v1

    2020-02-07
    Datasets added in this release
    Release note
    DNAs extracted from matched tumor and non-tumor tissues from 17 patients with lung adenocarcinoma were used for the whole exome sequencing (fastq files). DNA libraries were established with a SureSelect XT Human All Exon system and sequenced by Illumina HiSeq 2500 system (paired-end; 100 bp).