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Status |
Public on Sep 30, 2023 |
Title |
PAX3-FOXO1 drives tumor formation from multiple lineages [scRNA-seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Comparison of fusion-positive rhabdomyosarcoma tumors from endothelial and myogenic origins to wild-type tissue shows few differences between the two tumors.
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Overall design |
We performed single cell gene expression profiling analysis fo scRNA-seq data for multiple endothelial cell types and two genetically engineered mouse models of rhabdomyosarcoma.
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Contributor(s) |
Searcy MB, Jin H, Hatley ME |
Citation(s) |
37968277 |
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Submission date |
Nov 18, 2022 |
Last update date |
Jan 03, 2024 |
Contact name |
Hongjian Jin |
E-mail(s) |
hongjian.jin@STJUDE.ORG
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Organization name |
St Jude Children's Research Hospital
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Department |
Center for Applied Bioinformatics
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Street address |
262 Danny Thomas Place
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City |
Memphis |
State/province |
TN |
ZIP/Postal code |
38015 |
Country |
USA |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (13)
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This SubSeries is part of SuperSeries: |
GSE218274 |
PAX3-FOXO1 expression in endothelial progenitors dictates myogenic reprogramming and rhabdomyosarcoma identity |
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Relations |
BioProject |
PRJNA903207 |