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Items: 4

1.

Pervasive H3K27 acetylation leads to ERV expression and a therapeutic vulnerability in H3K27M gliomas

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
210 Samples
Download data: BED, NARROWPEAK
Series
Accession:
GSE128745
ID:
200128745

PubMed Full text in PMC Similar studies

2.

Pervasive H3K27 acetylation leads to ERV expression and a therapeutic vulnerability in H3K27M gliomas [RNA-Seq]

(Submitter supplied) Epigenetic alterations are recurrently observed in cancer and are the subject of active therapeutic investigations. Midline high-grade gliomas (HGGs) are deadly brain tumors characterized by lysine-to-methionine substitutions at position 27 in histone 3 (H3) variants (denoted H3K27M), which are core components of the nucleosome. H3K27M, the first event in midline HGG development, results in a drastic loss of the repressive histone mark H3K27 tri-methylation (H3K27me3), and a notable increase in H3K27 acetylation (H3K27ac), a mark associated with active chromatin and cellular identity. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL16791 GPL20301 GPL11154
96 Samples
Download data: TXT
Series
Accession:
GSE117446
ID:
200117446

PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector

3.

Illumina HiSeq 4000 (Homo sapiens)

Organism:
Homo sapiens
8519 Series
195580 Samples
Download data
Platform
Accession:
GPL20301
ID:
100020301

4.

BT245-KO-C2

Organism:
Homo sapiens
Source name:
Tumor-derived cell-line
Platform:
GPL20301
Series:
GSE117446 GSE128745
Download data
Sample
Accession:
GSM3294960
ID:
303294960

SRA Run Selector

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db=gds|term=GSM3294960[Accession]|query=1|qty=2|blobid=MCID_67491036462e1a751e18a6b6|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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