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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.

Dataset ID

JGAD000784

Type of data
NGS (WGS)
Access criteria
Controlled-access (Type I)
Total data volume
271 GB
File formats
  • FASTQ
Research
hum0426
Date published
2024-08-02
Date modified
2024-08-02

Analysis method

WGS

Materials and participants
hereditary cancer syndromes (ICD10: C00-C97): 33 cases
peripheral blood cells (normal leukocytes): 33 samples
  • Health status
    Affected
  • Subject count
    33 (Individual)
Disease
hereditary cancer syndromes
Sample description
DNAs extracted from peripheral blood cells
  • Tissue
    Peripheral blood
  • Tumor / normal
    Normal
Sample provider
N/A
Experimental method
WGS
Target
N/A
Reagent kit
Ligation Sequencing Kit (SQK-LSK110)
Ligation Sequencing Kit (SQK-LSK114)
Fragmentation
g-TUBE (Covaris)
Platform
Oxford Nanopore Technologies GridION
Read type
Single-end
Read length
600 bp (N50, approx.)
Target region: 9000 bp (N50, approx.)