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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

JGAD000017

Type of data
NGS (Exome)
Access criteria
Controlled-access (Type I)
Total data volume
12.6 GB
File formats
  • BAM
Research
hum0022
Date published
2020-09-28
Date modified
2020-11-18
DDBJ Search
JGAD000017 (opens in a new tab)
JGA Study
JGAS000017 (opens in a new tab)

Analysis method

WES

Materials and participants
One DCL patient (cells were obtained at the points of initial acute myeloid leukemia, remission stage, relapsed stage, and DCL at late stage). One donor (normal peripheral blood)
  • Health status
    Mixed
  • Subject count
    2 (Individual)
Sample description
Genomic DNAs were extracted from leukemic cells from bone marrow aspirate or peripheral blood.
BM-P1: leukemia, BM-P2: remission, BM-P3: relapse, BM-P4: donor cell-derived leukemia at a late stage, BM-D1: peripheral blood of the transplant donor
  • Tissue
    Bone marrow, Oral mucosa, Peripheral blood
  • Tumor / normal
    Mixed
Sample provider
N/A
Experimental method
WES
Target
N/A
Reagent kit
SureSelect
Fragmentation
Ultrasonic fragmentation (Covaris S220)
Platform
Illumina HiSeq 2000
Read type
Paired-end
Read length
100 bp
Reference genome
GRCh37
Phenotype data
Included
Data use policy
NBDC data sharing policy (JGAP000001)