HRA000736
Title:
Whole genome sequencing based mutational scanning in Klinefelter Syndrome patients
Release date:
2021-03-23
Description:
Current understanding holds that Klinefelter syndrome (KS) is not inherited, but oc-curs randomly during meiosis. Whether there is any genetic basis for the origin of KS is unknown.To study the potential genetic basis for paternal-origin KS, we performed WES in 108 unrelated KS patients with the classical 47, XXY karyotype.
Data Accessibility:   
Controlled access Request Data
BioProject:
Study type:
Disease Study
Disease name:
Klinefelter's syndrome
Data Access Committee

For each controlled access study, there is a corresponding Data Access Committee(DAC) to determine the access permissions. Access to actual data files is not managed by NGDC.


DAC NO.:
DAC name:
KS Data Access Committee
Contact person:
Li Wei
Email:
leways@ioz.ac.cn
Description:
Data Access Committee for whole genome sequencing results based mutational scanning in 108 Klinefelter Syndrome patients
Individuals & samples
Submitter:   Chen Zi-Jiang / chenzijiang@hotmail.com
Organization:   Shandong University
Submission date:   2021-03-18
Requests:   1