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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.

Research ID

hum0389-v1Release info

Latest

Research title

Genetic analysis of fetal developmental abnormalities

Research overview

Aims
To elucidate genetic etiologies of abnormal development and growth observed in fetuses and placentas through genomic and epigenomic analyses, and to apply knowledge from new discoveries to improve perinatal management.
Methods
Capture methyl-seq (Agilent SureSelect XT Methyl-Seq)
Participants/materials
Capture methyl-seq data for four genomic DNA samples from peripheral blood cells of healthy women
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000734NGS (Capture Methyl-seq)
  • Capture Methyl-seq
Controlled-access (Type I)2023-03-23

Data provider

Principal investigator
Kazuhiko Nakabayashi
Affiliation
Division of Developmental Genomics, Department of Maternal-Fetal Biology, Research Institute, National Center for Child Health and Development

Research projects

NameURL
Diagnosis of rare diseases and elucidation of molecular pathological states by using epigenetic information
N/A

Grants

NameTitleProject number
Practical Research Project for Rare / Intractable Diseases, Japan Agency for Medical Research and Development (AMED)
Diagnosis of rare diseases and elucidation of molecular pathological states by using epigenetic information
  • JP22ek0109489

Related publications

TitleDOIDataset ID
A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion
https://doi.org/10.21203/rs.3.rs-2173809/v1 (opens in a new tab)

Controlled access users

No use of the controlled access data has been recorded.