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Items: 3

1.

An allele-aware approach identifies altered nuclear associations of the contracted D4Z4 array at the FSHD locus

(Submitter supplied) Facioscapulohumeral dystrophy (FSHD) is caused by a deletion in a D4Z4 macrosatellite repeat array in the 4q subtelomere that leads to somatic de-repression of the transcription factor DUX4. It is not fully understood how array contractions cause de-repression, but they alter the local chromatin structure of D4Z4, resulting in loss of heterochromatic markers. In order to determine whether pathogenic contractions also alter the nuclear organization of the FSHD locus, we designed an allele-aware, high-throughput circular chromosome conformation capture assay (4C-seq) that distinguishes the two 4q copies of the locus from each other and from a paralogous locus in the 10q subtelomere. more...
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL11154 GPL10999
10 Samples
Download data: TXT
Series
Accession:
GSE40673
ID:
200040673
2.

Illumina Genome Analyzer IIx (Homo sapiens)

Platform
Accession:
GPL10999
ID:
100010999
3.

Control 1 Replicate 2

Organism:
Homo sapiens
Source name:
MB-NR-209
Platform:
GPL10999
Series:
GSE40673
Download data: TXT
Sample
Accession:
GSM999060
ID:
300999060
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db=gds|term=GSM999060[Accession]|query=1|qty=2|blobid=MCID_66567c8be795547e5fd3e6ff|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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