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Items: 3

1.

De Novo Copy Number Variations (CNVs) in ESC Derived from Intact and ST Blastocysts

(Submitter supplied) Because ST embryos may be at risk of procedure related chromosomal or sub-chromosomal abnormalities, we biopsied and examined expanded blastocysts derived from ST and control embryos. We examined copy number variations (CNVs) by SNP array to explore possible subchromosomal abnormalities (deletion or duplication) in selected ST ESCs. De novo CNVs were detected in both ST and intact controls but none carried clinical significance (Table S3 in the Supplementary Appendix).
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL19718
12 Samples
Download data: IDAT, TXT
Series
Accession:
GSE87897
ID:
200087897

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2.

IIllumina Infinium human CytoSNP-850K BeadChip

(Submitter supplied) See manufacturer's website
Organism:
Homo sapiens
15 Series
176 Samples
Download data: CSV
Platform
Accession:
GPL19718
ID:
100019718

3.

ED78

Organism:
Homo sapiens
Source name:
ESC-derived line
Platform:
GPL19718
Series:
GSE87897
Download data: IDAT
Sample
Accession:
GSM2342514
ID:
302342514

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db=gds|term=GSM2342514[Accession]|query=1|qty=2|blobid=MCID_674cc9cf30e6852f8a87f9cd|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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