NBDC Research ID: hum0061.v1
SUMMARY
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
Dataset ID | Type of Data | Criteria | Release Date |
---|---|---|---|
JGAS000057 | NGS (Exome) | Controlled-access (Type I) | 2017/02/20 |
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MOLECULAR DATA
Participants/Materials | Siblings developed multiple primary lung cancers |
Targets | Exome |
Target Loci for Capture Methods | - |
Platform | Illumina [HiSeq 2000] |
Library Source | gDNA extracted from peripheral blood cells of siblings developed multiple primary lung cancers |
Cell Lines | - |
Library Construction (kit name) | BGI exome sequencing service |
Fragmentation Methods | BGI exome sequencing service |
Spot Type | Paired-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) | 90 bp |
Japanese Genotype-phenotype Archive Dataset ID | JGAD000057 |
Total Data Volume |
29 GB Data files: 8 (fastq) Analysis files: 4 (vcf [ref: hg19]) |
Comments (Policies) | NBDC policy |
DATA PROVIDER
Principal Investigator: Kikuya Kato
Affiliation: Osaka Medical Center for Cancer and Cardiovascular Diseases
Project / Group Name: -
Funds / Grants (Research Project Number):
Name | Title | Project 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 | - |
The Charitable Trust Osaka Cancer Research Foundation | Searching causative genetic aberrations of familial or sporadic rare tumors by genome analyses of patients | - |
The Osaka Medical Research Foundation for Intractable Diseases | Searching causative genes of familial cancers by genome analyses of sibling patients with rare cancer | - |
PUBLICATIONS
Title | DOI | Dataset ID | |
---|---|---|---|
1 | Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs | doi: 10.1101/mcs.a001032 | JGAD000057 |
2 |
USRES (Controlled-access Data)
Principal Investigator | Affiliation | Country/Region | Research Title | Data in Use (Dataset ID) | Period of Data Use |
---|---|---|---|---|---|
Hirofumi Nakaoka | Department of Cancer Genome Research, Sasaki Institute | Japan | Genetic analysis of lung cancer | JGAD000057 | 2022/08/06-2023/03/31 |