NBDC Research ID: hum0035.v2

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SUMMARY

Aims: To explore genetic alterations in solid tumors, we performed genome wide analysis using next generation sequencing methods.

Methods:

JGAS000036: Whole exome sequencing (WES) for 16 rhabdomyosarocoma (RMS) and 7 pleuropulmonary blastoma (PPB) patients using tumor tissues and corresponding normal blood cells (non-tumor tissues) were performed. Relapsed tumor tissues were also analyzed in total of 5 cases.

JGAS000046: SNP-chip analysis and targeted amplicon deep sequencing were performed using tumor tissues and corresponding normal blood cells (non-tumor tissues) from 522 neuroblastoma (NB) patients and 39 neuroblastoma cell lines.

JGAS000088: SNP-chip and WES analyses were performed using tumor tissues and corresponding normal blood cells (non-tumor tissues) from 10 pancreatoblastoma (PBL) patients. Methylation array and RNA-seq analyses were performed using only tumor tissues.

Participants/Materials:

JGAS000036: 16 RMSs and 7 PPBs

JGAS000046: 522 NBs and 39 neuroblastoma cell lines

JGAS000088: 10 PBLs

URL: http://www.h.u-tokyo.ac.jp/vcms_lf/release_20150703.pdf

 

Dataset IDType of DataCriteriaRelease Date
JGAS000036 NGS (Exome) for RMS and PPB Controlled-access (Type I) 2015/09/16
JGAS000046

SNP-chip for NB

Target amplicon deep sequencing (NGS) for NB

Controlled-access (Type I) 2017/12/26
JGAS000088

SNP-chip for PBL

Methylation array for PBL

NGS (Exome) for PBL

NGS (RNA-seq) for PBL

Controlled-access (Type I) 2017/12/26

*Release Note  

*Data users need to apply an application for Using NBDC Human Data to reach the Controlled-access Data. Learn more

 

MOLECULAR DATA

JGAS000036, JGAS000088 (Exome)

Participants/Materials 16 RMSs, 7 PPBs, and 10 PBLs
Targets Exome
Target Loci for Capture Methods -
Platform Illumina [HiSeq 2000/2500]
Library Source DNA extracted form tumor tissues and peripheral blood cells as non-tumor tissues
Cell Lines -
Library Construction (kit name) SureSelect Human ALL Exon kit (50Mb kit, v4/v5)
Fragmentation Methods Ultrasonic fragmentation (Covaris S220)
Spot Type Paired-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 75-108 bp
Japanese Genotype-phenotype Archive Dataset ID

JGAD000036

EGAD00001000822 / EGAS00001000662 (PPB)

EGAD00001001105 / EGAS00001000884 (RMS)

JGAD000088

Total Data Volume

JGAD000036: 497.04 GB (bam [ref: hg19])

JGAD000088: 179.80 GB (bam [ref: hg19])

Comments (Policies) NBDC policy

 

JGAS000046, JGAS000088 (SNP-chip)

Participants/Materials

522 NBs (*sample list used in the paper)

39 neuroblastoma cell lines

10 PBLs

Targets SNP-chip
Target Loci for Capture Methods
Platform Affymetrix [GeneChip Human Mapping 250k Nspl / Cytoscan HD]
Library Source DNAs extracted form neuroblastoma cell lines, tumor tissues, and peripheral blood cells as non-tumor tissues
Cell Lines -
Reagents (Kit, Version) Affymetrix Cytoscan HD kit
Genotype Call Methods (software) Copy Number for GeneChip software (CNAG) and allele-specific copy-number analysis using anonymous references (AsCNAR)
Marker Number

GeneChip Human Mapping 250K Nsp Array : 262,264 CNVs

CytoScan HD Array : 2,696,550 CNVs

Japanese Genotype-phenotype Archive Dataset ID

JGAD000046

JGAD000088

Total Data Volume

JGAD000046: 32.42 GB (CEL)

JGAD000088: 179.80 GB (CEL)

Comments (Policies) NBDC policy

 

JGAS000046 (Target amplicon deep sequencing)

Participants/Materials 522 NBs
Targets Target Capture
Target Loci for Capture Methods

159 cases (NB_001~NB_159):

CHEK1, MRE11A, H2AFX, TP53, BRCA1, CHEK2, BARD1

500 cases (*see sample list):

ALK, MYCN, ATRX, ARID1A, ARID1B, PHOX2B, PTPN11, HRAS, KRAS, NRAS

Platform Illumina [Hiseq 2000 / Miseq]
Library Source DNAs extracted form neuroblastoma (tumor tissues)
Cell Lines -
Library Construction (kit name) The NEBNext Ultra DNA Library Prep Kit for Illumina
Fragmentation Methods Ultrasonic fragmentation (Covaris E220)
Spot Type Paired-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 100 bp or 150 bp
Mapping BWA
Mutation Detection Methods SAMtools
Japanese Genotype-phenotype Archive Dataset ID JGAD000046
Total Data Volume 32.42 GB (xlsx [ref: hg19])
Comments (Policies) NBDC policy

 

JGAS000088 (Methylation array)

Participants/Materials 10 PBLs
Targets Methylation array
Target Loci for Capture Methods -
Platform Illumina [Infinium MethylationEPIC]
Library Source DNAs extracted form pancreatoblastoma (tumor tissues)
Cell Lines -
Library Construction (kit name) Infinium MethylationEPIC kit
Algorithms for Calculating Methylation-rate (software) -
Filtering Methods -
Normalization of microarray -
Probe Number 450K probes (raw data)
Japanese Genotype-phenotype Archive Dataset ID JGAD000088
Total Data Volume 179.80 GB (idat)
Comments (Policies) NBDC policy

 

JGAS000088 (RNA-seq)

Participants/Materials 10 PBLs
Targets RNA-seq
Target Loci for Capture Methods -
Platform Illumina [HiSeq 2500]
Library Source RNAs extracted form pancreatoblastoma (tumor tissues)
Cell Lines -
Library Construction (kit name)

BioLabs NEBNext Ultra RNA Library Prep Kit for Illumina

Illumina TruSeq RNA Sample Preparation Kit v2

Fragmentation Methods included in the above library construction kit
Spot Type Paired-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 108 bp
Japanese Genotype-phenotype Archive Dataset ID JGAD000088
Total Data Volume 179.80 GB (raw array data)
Comments (Policies) NBDC policy

 

DATA PROVIDER

Principal Investigator: Junko Takita

Affiliation: Graduate School of Medicine, The University of Tokyo

Group Name: Department of Pediatrics, Hematology/Oncology Group

Project Name: Project for Development of Innovative Research on Cancer Therapeutics -Investigation of novel molecular targets of intractable pediatric solid tumors using integrated genetic analysis-

Funds / Grants (Research Project Number):

NameTitleProject Number
Project for Development of Innovative Research on Cancer Therapeutics (P-DIRECT), Japan Agency for Medical Research and Development (AMED) Investigation of novel molecular targets of intractable pediatric solid tumors using integrated genetic analysis 157100000120
KAKENHI Grant-in-Aid for Scientific Research (B) Studies on clonal evolutions which regulate metastasis and relapse in pediatric solid tumors using spatiotemporal and comprehensive genome-wide analysis 26293242

 

PUBLICATIONS

TitleDOIDataset ID
1 Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma. doi: 10.1038/ncomms8557 JGAD000036 EGAD00001001105
2 Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma. doi: 10.1158/0008-5472.CAN-13-2470 JGAD000036 EGAD00001000822
3 Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis. doi: 10.18632/oncotarget.22495 JGAD000046
4 Integrated molecular characterization of the lethal pediatric cancer pancreatoblastoma. doi: 10.1158/0008-5472.CAN-17-2581 JGAD000088

 

USERS (Controlled-access Data)

Principal Investigator: Affiliation: Data in Use (Dataset ID)Period of Data Use