Dataset features

Specifications


Application: BS-seq analysis
Number of samples: 4
Release date: May 29 2015
Last update date: Jan 23 2018
Access: Public
Diseases: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Scoliosis
Dataset link Congenital scolisis may be associated with both of rare mutation and allele-specific methylation

Experimental Protocol


DNA was extracted from peripheral blood of a monozygotic twin pair that was discordant for CS, with T-P affected with CS and T-H non-affected. Followed by MeDIP-seq and exome-seq.

Repositories


GEO

GSE58104

ENA

SRP042379

BioProject

PRJNA248908

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Contact


Zhixiang Yan