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Items: 3

1.

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases

(Submitter supplied) The most common congenital heart disease (CHD) is the ventricular septal defect (VSD), which is also a subfeature of Tetralogy of Fallot (TOF) representing the most common form of cyanotic CHD. The underlying causes for the majority of CHDs are still unclear and most probably consist of combinations of genetic, epigenetic and environmental factors. DNA methylation is the most widely studied epigenetic modification and several cardiac regulators have already been shown to be differentially methylated in CHD patients. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL11154
23 Samples
Download data: TXT
Series
Accession:
GSE62629
ID:
200062629

PubMed Similar studies SRA Run Selector

2.

Illumina HiSeq 2000 (Homo sapiens)

Organism:
Homo sapiens
10547 Series
183607 Samples
Download data
Platform
Accession:
GPL11154
ID:
100011154

3.

TOF-08 TOF

Organism:
Homo sapiens
Source name:
right ventricle
Platform:
GPL11154
Series:
GSE62629
Download data: TXT
Sample
Accession:
GSM1530474
ID:
301530474

SRA Run Selector

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db=gds|term=GSM1530474[Accession]|query=25|qty=2|blobid=MCID_672b356ec619b038bd15ebb8|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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