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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 hum0018

  • hum0018-v2

    2025-07-16
    Datasets added in this release
    Release note
    gDNA/RNA extracted from peripheral blood cells or brain tissues of patients with 69 Charcot-Marie-Tooth disease (CMT), 21 Frontotemporal dementia (FTD), 121 Familial amyotrophic lateral sclerosis (Familial ALS), 85 Myopathy, 490 Sporadic amyotrophic lateral sclerosis (Sporadic ALS), 9 Motor neuron disease (MND) and 465 Spastic paraplegia were used for whole exome sequencing, whole genome sequencing and RNA sequencing analyses (fastq format files).

  • hum0018-v1

    2015-02-03
    Datasets added in this release
    Release note
    gDNAs extracted from peripheral blood cells of 14 patients with multiple system atrophy and 7 healthy control subjects were used for Exome sequencing analysis (fastq format files). Exons were captured using the SureSelect Human All Exon 50 Mb Kit and multiplex sequence was performed with the Illumina HiSeq 2000 sequencer (100 bp, Paired-end).