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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.

Research ID

hum0426-v1Release info

Latest

Research title

Diagnosis and Research on Familial, Young-onset and Hereditary Cancers

Research overview

Aims
This study aims to 1) identify unknown causative genes, modifier genes, and their mutations in cancers suspected to be hereditary, and 2) accumulate knowledge on genotype-phenotype relationships, based on a multicenter cooperative system and network for genetic diagnosis of hereditary tumors.
Methods
DNA sequencing using adaptive sampling with GridION nanopore sequencer
Participants/materials
33 cases of hereditary cancer syndromes (blood)
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000784NGS (WGS)
  • WGS
Controlled-access (Type I)2024-08-02

Data provider

Principal investigator
Yuichi Shiraishi
Affiliation
Division of Genome Analysis Platform Development, National Cancer Center Research Institute

Research projects

No research projects.

Grants

NameTitleProject number
National Cancer Center Research and Development Funds
Establishing a Research Foundation and Verifying Clinical Utility Using Long-Read Sequencing
  • 2021-A-3

Related publications

TitleDOIDataset ID
Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes.
https://doi.org/10.1038/s41525-024-00394-z (opens in a new tab)

Controlled access users

No use of the controlled access data has been recorded.