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| Status |
Public on Apr 27, 2023 |
| Title |
Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation [RNA-seq Fibro] |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
|
| Summary |
We performed gene expression profiling analysis using data obtained from RNA-seq of BOS patient and control individual fibroblast samples to dissect the transcriptomic effects of truncating ASXL1 mutations.
We performed gene expression profiling analysis using data obtained from RNA-seq of BOS patient and control individual fibroblast samples.
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| |
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| Overall design |
Comparative gene expression profiling analysis of RNA-seq data for Bohring-Opitz syndrome patient blood samples and control blood samples.
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| |
|
| Contributor(s) |
Lin I, Wei A |
| Citation(s) |
37053013 |
| |
| Submission date |
Apr 26, 2023 |
| Last update date |
Jul 27, 2023 |
| Contact name |
Valerie Arboleda |
| E-mail(s) |
VArboleda@mednet.ucla.edu
|
| Organization name |
UCLA
|
| Street address |
615 Charles E. Young Drive South
|
| City |
Los Angeles |
| ZIP/Postal code |
90095 |
| Country |
USA |
| |
|
| Platforms (1) |
| GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
|
| Samples (14)
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| This SubSeries is part of SuperSeries: |
| GSE230696 |
Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation |
|
| Relations |
| BioProject |
PRJNA962130 |
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