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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 hum0006

  • hum0006-v6

    2026-06-03
    Datasets added in this release
    Release note
    DNAs/RNAs obtained from normal left frontal lobe tissue from a glioma patient were used for the FLeCS-seq, SMART-seq, RNA-seq, short-read WGS and ultralong-read WGS analyses. Fastq or bam files are provided.

  • hum0006-v5

    2022-08-08
    Datasets added in this release
    Release note
    DNAs extracted from 12 cerebral cavernous malformations, 1 vertebral hemangioma, 3 orbital cavernous malformations and respective paired peripheral blood samples were used for the target capture sequencing analysis. Fastq files are provided.

  • hum0006-v4

    2019-02-13
    Datasets added in this release
    Release note
    Analysis data about 94 gliomas (114 samples) were added (JGAS000146).
    • Exome (JGAD000215, JGAD000218) : glioma: 12 cases (25 tumor samples, 12 non-tumor samples)
    DNAs extracted from gliomas and peripheral blood were used for the whole exome sequencing. Exons were narrowed down by using of SureSelect Human All Exon v.4 and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • RNA-seq (JGAD000216, JGAD000219) : glioma: 23 cases (31 samples)
    RNAs extracted from gliomas were used for RNA-seq. RNA liberally builded using TruSeq Stranded Total RNA Library Prep Kit and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • Methylation array (JGAD000217) : glioma: 93 cases (113 samples)
    DNAs extracted from gliomas were performed with methylation analysis using Illumina HumanMethylation 450 BeadChip.

  • hum0006-v3

    2017-09-01
    Datasets added in this release
    Release note
    Analysis data about 39 gliomas (17 diffuse cerebellar gliomas, 14 cerebral glioblastomas, 8 thalamic gliomas) were added (JGAS000106).
    • Exome: diffuse cerebellar glioma (ICD10:C71): 17 cases (34 samples)
    DNAs extracted from brain tumors (diffuse cerebellar gliomas, cerebral glioblastomas, thalamic gliomas) and peripheral blood were used for the whole exome sequencing. Exons were narrowed down by using of SureSelect Human All Exon v.4 and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • RNA-seq: diffuse cerebellar glioma: 14 cases (14 samples), cerebral glioblastoma: 8 cases (8 samples)
    RNAs extracted from brain tumors (diffuse cerebellar glioma, cerebral glioblastoma) were used for RNA-seq (bam and fastq). RNA liberally builded using TruSeq Stranded Total RNA Library Prep Kit and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • Methylation array: diffuse cerebellar glioma: 17 cases (17 samples), thalamic glioma: 14 cases (14 samples)
    DNAs extracted from brain tumors (diffuse cerebellar glioma, thalamic glioma) were performed with methylation analysis using Illumina HumanMethylation 450 BeadChip.

  • hum0006-v2

    2017-06-05
    Datasets added in this release

    No datasets were added.

    Release note
    Analysis data about 16 oligodendrogliomas were added to JGAS000004.
    • Exome: 48 samples
    DNAs extracted from brain tumors (oligodendrogliomas) and peripheral blood were used for the whole exome sequencing. Exons were narrowed down by using of SureSelect Human All Exon v.4 and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • RNA-seq: 27 samples
    RNAs extracted from brain tumors (oligodendrogliomas) were used for RNA-seq (bam and fastq). RNA liberally builded using TruSeq Stranded Total RNA Library Prep Kit and read by Illumina HiSeq 2000 (paired-end: 100 bp)
    • Methylation array: 30 samples
    DNAs extracted from brain tumors (oligodendrogliomas) were performed with methylation analysis using Illumina HumanMethylation 450 BeadChip.

  • hum0006-v1

    2014-01-31
    Datasets added in this release
    Release note
    DNAs extracted from brain tumors (6 astrocytomas) and peripheral blood were used for the whole exome sequencing (bam files). Exons were narrowed down by using of SureSelect Human All Exon v.4 and read by Illumina HiSeq 2000 (paired-end: 100 bp)