Dataset ID
JGAD000781
- Type of data
- NGS (RNA-seq)
- Access criteria
- Controlled-access (Type I)
- Total data volume
- 90.8 GB
- File formats
- FASTQ
- Research
- hum0431
- Date published
- 2024-01-25
- Date modified
- 2024-01-25
- DDBJ Search
- JGAD000781 (opens in a new tab)
- JGA Study
- JGAS000651 (opens in a new tab)
Analysis method
RNA-seq
- Materials and participants
- Human iPSCs (HPS4290:201B7-Ff) introduced single variants identified in patients with ASD (ICD10: F840)
1) Mutant iPSC lines with the chr7:g.26200781C>T variant and the single PAM sequence: 2 samples
Control lines with a single PAM sequence: 2 samples
2) Mutant iPSC lines with the chr22:g.19179942C>T variant and the single PAM sequence: 3 samples
Control lines with a single PAM sequence: 2 samples - Health statusMixed
- Subject count9 (Sample)
- Disease
- ASD (F840)
- Sample description
- RNAs extracted from mutant iPSCs
- TissueiPSC
- Tumor / normalNormal
- Cell line
- 201B7-Ff
iPSC - Sample provider
- RIKEN BRC
- Experimental method
- RNA-seq
- Target
- N/A
- Reagent kit
- NEBNext Ultra RNA Library Prep Kit for Illumina
- Fragmentation
- included in the above library construction kit
- Platform
- Illumina NovaSeq 6000
- Read type
- Paired-end
- Read length
- 150 bp
- Data use policy
- NBDC data sharing policy (JGAP000001)