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| Status |
Public on Dec 16, 2011 |
| Title |
Somatic copy number variants in monozygotic twins and elderly single-born individuals |
| Organism |
Homo sapiens |
| Experiment type |
SNP genotyping by SNP array
Genome variation profiling by SNP array
|
| Summary |
We perfomed copy number analysis of young and old monozygotic twin pairs and young and old single-born individuals to identify somatic copy number changes that occur with age in blood DNA.
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| Overall design |
DNA from peripheral blood was run on Illumina genotyping arrays and the R and B-allele-frequency data were used to identify somatic copy number events. The young Samples were omited because all young twins lacked CNVs in the >1 megabase range.
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| Contributor(s) |
Absher DM, Dumanski JP |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| |
| Submission date |
Dec 15, 2011 |
| Last update date |
Jan 14, 2015 |
| Contact name |
Devin Absher |
| E-mail(s) |
[email protected]
|
| Organization name |
HudsonAlpha Institute for Biotechnology
|
| Street address |
601 Genome Way
|
| City |
Huntsville |
| State/province |
AL |
| ZIP/Postal code |
35806 |
| Country |
USA |
| |
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| Platforms (2) |
| GPL6984 |
Illumina Human1M-Duov3 DNA Analysis BeadChip (Human1M-Duov3_B) |
| GPL8888 |
Illumina Human660W-Quad v1.0 BeadChip |
|
| Samples (6)
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| Relations |
| BioProject |
PRJNA151185 |
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