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Items: 3

1.

Tissue Specific Methylation and Expression Patterns of ADCA-DN Patients

(Submitter supplied) Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) is a late onset disorder, due to mutations in DNA methyltransferase type 1 (DNMT1). Yet our understanding of how these mutations in DNMT1 lead to the clinical phenotypes of ADCA-DN is still unclear. To address this, we used fibroblasts, induced pluripotent stem cells (iPSCs) and induced neurons (iNs) generated from patients with ADCA-DN and controls, to determine the underlining epigenomic changes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL20301 GPL21697
56 Samples
Download data: TXT
Series
Accession:
GSE126890
ID:
200126890

Analyze with GEO2RSRA Run Selector

2.

NextSeq 550 (Homo sapiens)

Organism:
Homo sapiens
1500 Series
44597 Samples
Download data
Platform
Accession:
GPL21697
ID:
100021697

3.

F01-1iPSC RNA-Seq

Organism:
Homo sapiens
Source name:
induced pluripotent stem cell
Platform:
GPL21697
Series:
GSE126890
Download data: TXT
Sample
Accession:
GSM3617771
ID:
303617771

SRA Run Selector

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db=gds|term=GSM3617771[Accession]|query=1|qty=2|blobid=MCID_674c283ad8260840384c5cdf|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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