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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

JGAD000493

Type of data
NGS (Exome)
Access criteria
Controlled-access (Type I)
Total data volume
34.7 KB
File formats
  • XLSX
Research
hum0202
Date published
2021-11-05
Date modified
2021-11-05
DDBJ Search
JGAD000493 (opens in a new tab)
JGA Study
JGAS000379 (opens in a new tab)

Analysis method

WES

Materials and participants
Congenital hearing loss (ICD10: H905):
3 cases and their parents (Total: 9 samples)
  • Health status
    Mixed
  • Subject count
    9 (Individual)
Disease
  • Congenital hearing loss
Sample description
DNAs extracted from peripheral blood cells
  • Tissue
    Peripheral blood
  • Tumor / normal
    Normal
Sample provider
N/A
Experimental method
WES
Target
46 variants
Reagent kit
Nextera Rapid Capture Exome Kit
SureSelect Human All Exon V5
Fragmentation
Ultrasonic fragmentation (Covaris)
Platform
Illumina HiSeq 2500
Illumina HiSeq 4000
Read type
Paired-end
Read length
126 bp
Reference genome
GRCh37
Data use policy
NBDC data sharing policy (JGAP000001)