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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

hum0061-v1Release info

Latest

Research title

Searching causative genes of familial tumors using whole genome / exome sequencing

Research overview

Aims
To identify causative genetic aberrations in multiple primary lung cancer
Methods
Whole exome sequencing (Illumina HiSeq 2000)
Participants/materials
Siblings developed multiple primary lung cancers
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000057NGS (Exome)
  • WES
Controlled-access (Type I)2020-09-28

Data provider

Principal investigator
Kikuya Kato
Affiliation
Osaka Medical Center for Cancer and Cardiovascular Diseases

Research projects

No research projects.

Grants

NameTitleProject number
KAKENHI Grant-in-Aid for Scientific Research (C)
Identification of causative genes for hereditary cancer by genome analyses of familial cancer cases and its application
  • 25430180
The Osaka Community Foundation
Searching causative genes of familial or sporadic rare tumors using whole gene sequencing
N/A
The Charitable Trust Osaka Cancer Research Foundation
Searching causative genetic aberrations of familial or sporadic rare tumors by genome analyses of patients
N/A
The Osaka Medical Research Foundation for Intractable Diseases
Searching causative genes of familial cancers by genome analyses of sibling patients with rare cancer
N/A

Related publications

TitleDOIDataset ID
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
https://doi.org/10.1101/mcs.a001032 (opens in a new tab)

Controlled access users

Principal investigatorAffiliationCountry/RegionResearch titlePeriod of data useDataset ID
Hirofumi NakaokaDepartment of Cancer Genome Research, Sasaki InstituteJapanGenetic analysis of lung cancer2022-08-17 – 2026-07-23