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Status |
Public on May 02, 2019 |
Title |
RNA-Seq of isogenic human iPS cell-derived cardiomyocytes with RBM20 mutations created by genome editing [RNA-Seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
RBM20 heterozygous (Het) and homozygous (Homo) R636S and homozygous 8-bp deletion (which causes nonsense-mediated decay) mutations were created by genome editing in an iPS cell line generated from a healthy male patient. Those cells were differentiated into cardiomyocytes by modulating the WNT signaling pathway, and then are subjected to the lactate purification method.
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Overall design |
RNAseq of iPS cell-derived cardiomyocytes with 4 different genotypes as replicates
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Contributor(s) |
Miyaoka Y, Mayerl SJ, Chan AH, Conklin BR, Salomonis N |
Citation(s) |
34732726 |
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Submission date |
May 02, 2018 |
Last update date |
Dec 02, 2021 |
Contact name |
Nathan Salomonis |
E-mail(s) |
nathan.salomonis@cchmc.org
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Organization name |
Cincinnati Children's Hospital
|
Department |
Biomedical Informatics
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Lab |
Nathan Salomonis
|
Street address |
3333 Burnet Avenue
|
City |
Cincinnati |
State/province |
OH |
ZIP/Postal code |
45229 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (21)
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GSM3124390 |
WTC11 RBM20 8-bp deletion Homo replicate 1 |
GSM3124391 |
WTC11 RBM20 8-bp deletion Homo replicate 2 |
GSM3124392 |
WTC11 RBM20 8-bp deletion Homo replicate 3 |
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This SubSeries is part of SuperSeries: |
GSE175886 |
RNA-Seq of isogenic human iPS cell-derived cardiomyocytes with RBM20 mutations created by genome editing |
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Relations |
BioProject |
PRJNA454577 |
SRA |
SRP144316 |