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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 hum0035

  • hum0035-v5

    2020-12-18
    Datasets added in this release
    Release note
    Analyses data about 30 high-risk neuroblastoma patients (JGAS000246) were added.
    • RNA-seq: RNA library was builded using BioLabs NEBNext Ultra RNA Library Prep Kit for Illumina, and read by Illumina HiSeq 2500 (paired-end: 108 bp).
    • Target Capture Sequencing: HiSeq 2000 and MiSeq (Illumina) were used for the sequencing analysis.

  • hum0035-v4

    2020-12-14
    Datasets added in this release
    Release note
    Analyses data about 51 patients with pediatric germ cell tumors (JGAS000204) were added.
    • SNP-chip: GeneChip Human Mapping 250k Nspl (Affymetrix) was used for genotyping.
    • Target Capture Sequencing: HiSeq 2000 and MiSeq (Illumina) were used for the sequencing analysis.
    • RNA-seq: RNA library was builded using BioLabs NEBNext Ultra RNA Library Prep Kit for Illumina or Illumina TruSeq RNA Sample Preparation Kit v2, and read by Illumina HiSeq 2500 (paired-end: 108 bp).
    • Methylation array: Infinium MethylationEPIC (Illumina) was used for the methylation analysis.

  • hum0035-v3

    2020-05-29
    Datasets added in this release
    Release note
    Analyses data about 59 hepatoblastoma (HBL) patients and 2 HBL cell lines (JGAS000188) were added.
    • SNP-chip: GeneChip Human Mapping 250k Nspl (Affymetrix) was used for genotyping.
    • Target Capture Sequencing: HiSeq 2000 and MiSeq (Illumina) were used for the sequencing analysis.
    • RNA-seq: RNA library was builded using BioLabs NEBNext Ultra RNA Library Prep Kit for Illumina or Illumina TruSeq RNA Sample Preparation Kit v2, and read by Illumina HiSeq 2500 (paired-end: 108 bp).
    • Methylation array: Infinium MethylationEPIC (Illumina) was used for the methylation analysis.

  • hum0035-v2

    2017-12-26
    Datasets added in this release
    Release note
    Analyses data about 522 neuroblastoma (NB) patients, 39 neuroblastoma cell lines (JGAS000046), and 10 pancreatoblastoma (PBL) patients (JGAS000088) were added.
    • SNP-chip: 39 neuroblastoma cell lines and tumor tissues and peropheral blood cells (non-tumor tissues) from 522 NBs and 10 PBLs
    GeneChip Human Mapping 250k Nspl (Affymetrix) was used for genotyping.
    • Target amplicon deep sequencing: tumor tissues from 522 NBs
    HiSeq 2000, MiSeq (Illumina) was used for genotyping.
    • Exome: tumor tissues and peripheral blood cells (as non-tumor tissues) from 10 PBLs
    Exons were narrowed down by using of SureSelect Human ALL Exon kit (50Mb kit, v4/v5) and read by Illumina HiSeq 2000/2500 (paired-end: 75-108 bp).
    • RNA-seq: tumor tissues from 10 PBLs
    RNA library was builded using BioLabs NEBNext Ultra RNA Library Prep Kit for Illumina or Illumina TruSeq RNA Sample Preparation Kit v2, and read by Illumina HiSeq 2500 (paired-end: 108 bp).
    • Methylation array: tumor tissues from 10 PBLs
    Infinium MethylationEPIC (Illumina) was used for methylation analysis.

  • hum0035-v1

    2015-09-16
    Datasets added in this release
    Release note
    DNAs extracted from fresh tumors and corresponding normal blood samples of 16 rhabdomyosarocoma and 7 pleuropulmonary blastoma patients were used for the whole exome sequencing (bam files) (JGAS000036). DNA fragments containing whole coding exons were concentrated using SureSelect Human ALL Exon kit (50Mb kit, v4) followed by 75-108 bp paired-end sequencing by Hiseq 2000/2500 (Illumina).