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Items: 4

1.

Domains of genomewide gene expression dysregulation in Down syndrome [ChIP-seq]

(Submitter supplied) Trisomy 21 (T21) is the most frequent genetic cause of cognitive impairment. To assess the perturbations of gene expression in T21, and to eliminate the noise of the genomic variability, we studied the transcriptome of fetal fibroblasts from a pair of monozygotic twins discordant for T21. Here we show that the differential expression between the twins is organized in domains along all chromosomes that are either up- or downregulated. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: TXT
Series
Accession:
GSE55506
ID:
200055506

PubMed Similar studies SRA Run Selector

2.

Illumina HiSeq 2500 (Homo sapiens)

Organism:
Homo sapiens
11814 Series
336528 Samples
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Platform
Accession:
GPL16791
ID:
100016791

3.

T2N H3K4me3 ChIP

Organism:
Homo sapiens
Source name:
twin 2_euploid_fetal primary fibroblasts_ChIP
Platform:
GPL16791
Series:
GSE55426 GSE55506
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Sample
Accession:
GSM1338344
ID:
301338344

SRA Run Selector

4.

T1DS H3K4me3 ChIP

Organism:
Homo sapiens
Source name:
twin 1_T21_fetal primary fibroblasts_ChIP
Platform:
GPL16791
Series:
GSE55426 GSE55506
Download data
Sample
Accession:
GSM1338343
ID:
301338343

SRA Run Selector

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db=gds|term=GSE55506[Accession]|query=1|qty=2|blobid=MCID_6649a8dd3844a3792a4aa753|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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