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Status |
Public on Nov 15, 2018 |
Title |
RNA-seq of synchronized S phase or G2 phase cells treated with an ATR inhibitor |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We performed RNA-seq in cells synchronized to S or G2 phase to identify genes that were transcriptionally regulated by ATR activity.
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Overall design |
RPE-1 cells were synchronized to late S (4 hours post-release from thymidine block), or to G2 phase (6 hours post-released from thymidine block) and either mock-treated or ATR-inhibited to identify genes that were transcriptionally controlled by ATR. An asynchronous control and an un-released from the thymidine block control were included. These 6 conditions were repeated in 3 independent experiments (total of 18 samples) and analyzed by RNA-seq.
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Contributor(s) |
Bocek M, Saldivar J, Cimprich K, Hamperl S |
Citation(s) |
30139873 |
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Submission date |
Jun 21, 2018 |
Last update date |
Jan 14, 2020 |
Contact name |
Karlene Anne Cimprich |
E-mail(s) |
cimprich@stanford.edu
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Organization name |
Stanford University
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Street address |
318 Campus Drive
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94025 |
Country |
USA |
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Platforms (1) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA477351 |
SRA |
SRP151048 |