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Status |
Public on May 10, 2016 |
Title |
Nfib promotes Metastasis through a Widespread Increase in Chromatin Accessibility [RNA-seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
We describe Nfib as an important regulator of chromatin accessibility in SCLC.
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Overall design |
We performed RNA-seq on three cell lines with either knockdown of Nfib expression or overexpression of Nfib. Cell lines 16T and KP1 were expressing iether a control vector or a vector expressing shRNA to Nfib, in duplicate Cell line KP22 were expressing either an empty vector or a vector expressing Nfib cDNA, in duplicate.
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Contributor(s) |
Denny S, Yang D, Sage J, Greenleaf W, Winslow M |
Citation(s) |
27374332 |
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Submission date |
May 09, 2016 |
Last update date |
May 15, 2019 |
Contact name |
William Greenleaf |
E-mail(s) |
wjg@stanford.edu
|
Organization name |
Stanford University
|
Street address |
279 Campus Drive
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE81258 |
Nfib promotes Metastasis through a Widespread Increase in Chromatin Accessibility |
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Relations |
BioProject |
PRJNA321071 |
SRA |
SRP074735 |