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Schedule: October 5th (Mon), 2026, 9:00 - October 7th (Wed), 2026, 15:00 (JST)
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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

JGAD000498

Type of data: SNP array
Access criteria: Controlled-access (Type I)
Total data volume: 3.3 GB
File formats: CSV
Research: hum0314
Date published: 2021-12-22
Date modified: 2021-12-22
DDBJ Search: JGAD000498 (opens in a new tab)
JGA Study: JGAS000383 (opens in a new tab)

Analysis method

Genotyping by array

Materials and participants: sporadic Alzheimer's disease (ICD10: G309, F009): 102 cases; Health status
Affected
Subject count
102 (Individual)
Disease: sporadic Alzheimer's disease (G309, F009)
Sample description: DNAs extracted from peripheral blood cells; Tissue
Peripheral blood
Tumor / normal
Normal
Sample provider: N/A
Experimental method: Genotyping by array
Target: N/A
Reagent kit: HumanOmniExpressExome BeadChip Kit
Platform: Illumina HumanOmniExpressExome
Analysis method: GenCall software (GenomeStudio)
Variant count: 962,215 SNVs (reference: 1,000 Genomes Project Phase 3)
Data use policy: NBDC data sharing policy (JGAP000001)