|
| Status |
Public on Jul 11, 2012 |
| Title |
Small non-coding differentially-methylated copy-number variants, involving lncRNAs, cause a lethal lung developmental disorder |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
Genome binding/occupancy profiling by genome tiling array
Other
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
23034409 |
| Submission date |
Jul 11, 2012 |
| Last update date |
Feb 05, 2013 |
| Contact name |
Pawel Stankiewicz |
| E-mail(s) |
pawels@bcm.edu
|
| Organization name |
Baylor College of Medicine
|
| Department |
Molecular Human Genetics
|
| Street address |
One Baylor Plaza
|
| City |
Houston |
| State/province |
TX |
| ZIP/Postal code |
77030 |
| Country |
USA |
| |
|
| Platforms (4)
|
| GPL15735 |
Agilent-030795 custom-designed human 16q24.1 region-specific 4x44K oligonucleotide microarray (hg19) |
| GPL15746 |
NimbleGen Human CGH 4.2M Whole-Genome Tiling Array v1.0 array [100710_HG19_WG_CGH_v1.0_UX1] |
| GPL15751 |
Agilent-022084 16q24.1_HD |
| GPL15783 |
NimbleGen custom human 3X720K CGH array [111205_HG19_PS_CGH] |
|
| Samples (14)
|
|
| This SuperSeries is composed of the following SubSeries:
|
| GSE38978 |
Detection of non-coding deletion CNVs upstream to FOXF1 [Agilent-022084] |
| GSE39254 |
Detection of non-coding deletion CNVs upstream to FOXF1 [Agilent-030795] |
| GSE39255 |
ChIP-chip analysis to determine GLI2 binding sites |
| GSE39256 |
FOXF1 promoter-putative enhancer chromatin looping |
| GSE39257 |
Genomic copy-number analysis in Alveolar capillary dysplasia (ACD) patient samples |
|
| Relations |
| BioProject |
PRJNA170413 |
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