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Items: 3

1.

Identification of a DNA methylation signature in blood from subjects affected by Down syndrome

(Submitter supplied) Down syndrome is characterized by a wide spectrum of clinical signs, which include cognitive and endocrine disorders and haematological abnormalities. Although it is well established that the causative defect of Down syndrome is the trisomy of chromosome 21, the molecular bases of Down syndrome phenotype are still largely unknown. We used the Infinium HumanMethylation450 BeadChip to investigate DNA methylation patterns in whole blood from 29 subjects affected by Down syndrome (DS), using their healthy relatives as controls (mothers and unaffected siblings). more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
87 Samples
Download data: TXT
Series
Accession:
GSE52588
ID:
200052588
2.

Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482)

(Submitter supplied) 1 difference between HumanMethylation450_15017482_v.1.1.bpm and HumanMethylation450_15017482_v.1.2.bpm: 1.1: 41636384,NEGATIVE,-99,Negative 604 1.2: 41636384,RESTORATION,Green,Restore Protocol: See manufacturer's website
Organism:
Homo sapiens
1661 Series
1 Related Platform
117595 Samples
Download data: BPM, CSV, TXT, XLSX
Platform
Accession:
GPL13534
ID:
100013534
3.

genomic DNA from peripheral blood, mother of a subject affected by Down syndrome, 2009

Organism:
Homo sapiens
Source name:
peripheral whole blood, subject 2009
Platform:
GPL13534
Series:
GSE52588
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Sample
Accession:
GSM1272183
ID:
301272183
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Supplemental Content

db=gds|term=GSM1272183[Accession]|query=1|qty=2|blobid=MCID_65dcbf3d22cedd048f45a644|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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