|
| Status |
Public on Nov 01, 2011 |
| Title |
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by array
Expression profiling by high throughput sequencing
Genome variation profiling by SNP array
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
22182939 |
| Submission date |
Feb 22, 2011 |
| Last update date |
May 15, 2019 |
| Contact name |
Jozef Gecz |
| Organization name |
SA Pathology
|
| Department |
Genetics Medicine
|
| Lab |
Neurogenetics
|
| Street address |
72 King William Rd
|
| City |
North Adelaide |
| State/province |
South Australia |
| ZIP/Postal code |
5006 |
| Country |
Australia |
| |
|
| Platforms (3) |
| GPL5175 |
[HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [transcript (gene) version] |
| GPL9115 |
Illumina Genome Analyzer II (Homo sapiens) |
| GPL13135 |
HumanOmniExpress BeadChip |
|
| Samples (32)
|
|
| This SuperSeries is composed of the following SubSeries: |
| GSE27125 |
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [mRNA profiling] |
| GSE27199 |
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [RNA-seq] |
| GSE27412 |
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [CNV] |
|
| Relations |
| BioProject |
PRJNA137227 |
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