NBDC Research ID: hum0302.v2

 

SUMMARY

Aims: To characterize iPS cell lines (healthy-donor iPS cell lines and disease-specific iPS cell lines), differentiation potential analysis (evaluation of differentiation potential into disease-causing cells and involved cells), disease-causing gene analysis, and whole genome analysis were performed.

Methods:

[JGAS000382] Hepatocytes were induced to differentiate from human iPS cells and collected on day 19. RNA was collected and strand-specific library preparation was performed by a PolyA selection method. The prepared library was sequenced by Novaseq6000. Sequencing was performed in a 2x150 bp PE configuration with a data output of about 6 Gb per sample (equivalent to about 20 million paired reads).

[JGAS000683] Kidney organoids were induced to differentiate from human iPS cells and collected on day 18. RNA was collected and strand-specific library preparation was performed by a PolyA selection method. The prepared library was sequenced by Novaseq6000. Sequencing was performed in a 2x150 bp PE configuration with a data output of about 6 Gb per sample (equivalent to about 20 million paired reads).

Participants/Materials: iPS cells derived from patients with Wilson's disease, juvenile nephron tabes (NPH1) patients and iPS cells derived from healthy donors

URL: https://acd.brc.riken.jp/en/

 

Dataset IDType of DataCriteriaRelease Date
JGAS000382 NGS (RNA-seq) Controlled-access (Type I) 2022/09/05
JGAS000683 NGS (RNA-seq) Controlled-access (Type I) 2024/03/18

*Release Note  

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

MOLECULAR DATA

JGAS000382 / JGAS000683

Participants/Materials

[JGAS000382]

Five samples of hepatocytes differentiated from iPS cells derived from patients with Wilson's disease (ICD10: E830)

One hepatocyte sample from a patient with Wilson's disease in which the ATP7B mutation was corrected by genome editing of iPS cells

Five samples of hepatocytes differentiated from healthy human-derived iPS cells

One hepatocyte sample in which the ATP7B mutation was introduced by genome editing of healthy donor-derived iPS cells

  [Total: 12 samples]

[JGAS000683]

6 kidney organoid samples induced from juvenile nephron tabes (NPH1) patient-derived iPS cells (ICD10: N19)

6 kidney organoid samples induced from juvenile nephron tabes (NPH1) patient-derived iPS cells overexpressing the responsible gene NPHP1

3 kidney organoid samples induced to differentiate from healthy human iPS cells

3 kidney organoid samples in which NPHP1 mutation was introduced by genome editing of healthy human iPS cells

  [Total: 18 samples]

Targets RNA-seq
Target Loci for Capture Methods -
Platform Illumina [NovaSeq 6000]
Library Source RNAs extracted from hepatocytes and kidney organoids differentiated from iPS cells
Cell Lines -
Library Construction (kit name) GeneWiz inc.'s protocol
Fragmentation Methods GeneWiz inc.'s protocol
Spot Type Paired-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 150 bp
Japanese Genotype-phenotype Archive Dataset ID

JGAD000497

JGAD000816

Total Data Volume 45.6 + 72.9 GB (fastq)
Comments (Policies) NBDC policy

 

DATA PROVIDER

Principal Investigator: Yohei Hayashi

Affiliation: RIKEN BioResource Research Center

Project / Group Name: iPS Cell Advanced Characterization and Development Team

URL: https://acd.brc.riken.jp/en/

Funds / Grants (Research Project Number):

NameTitleProject Number
- - -

 

PUBLICATIONS

TitleDOIDataset ID
1 Retinoids rescue ceruloplasmin secretion and alleviate oxidative stress in Wilson's disease-specific hepatocytes. doi: 10.1093/hmg/ddac080 JGAD000497

 

USRES (Controlled-access Data)

Principal InvestigatorAffiliationCountry/RegionResearch TitleData in Use (Dataset ID)Period of Data Use