|
Status |
Public on Feb 06, 2013 |
Title |
JQ1_4h_RNAseq |
Sample type |
SRA |
|
|
Source name |
S2-DRSC cells, JQ1, 4h
|
Organism |
Drosophila melanogaster |
Characteristics |
cell line: S2-DRSC treatment: JQ1 treatment duration: 4 hrs
|
Treatment protocol |
Cells were treated either with JQ1 or DMSO by adding the compound to the growth medium for the indicated time periods.
|
Growth protocol |
S2-DRSC cells were grown in Schneider's medium incl. 10% FCS.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using standard Trizol protocols for adherent cells. 4 microg of total RNA served as the starting material to construct the libraries using the TruSeq RNA Sample Prep Kit (Illumina) according to the manufacturer's instructions.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
BSSE-DSU-1738
|
Data processing |
Reads were aligned to the Drosophila genome release BDGP5 using the splice junction aware aligner TopHat (http://tophat.cbcb.umd.edu/) and standard parameters. Reads uniquely mapping to Drosophila gene sets (Ensembl release 64) were counted using the htseq-count script (http://www-huber.embl.de/users/anders/HTSeq/doc/count.html#count). Gene sets in GTF format were obtained from http://www.ensembl.org/info/data/ftp/index.html. Genome Build: 1738.counts: BDGP5
|
|
|
Submission date |
Feb 29, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Tobias Kockmann |
E-mail(s) |
[email protected]
|
Organization name |
ETHZ
|
Department |
D-BSSE
|
Lab |
Paro
|
Street address |
Mattenstr. 26
|
City |
Basel |
ZIP/Postal code |
4058 |
Country |
Switzerland |
|
|
Platform ID |
GPL13304 |
Series (2) |
GSE36180 |
Effects of pharmacologic FSH inhibition on gene expression |
GSE36450 |
The BET protein FSH functionally interacts with ASH1 to orchestrate global gene activity in Drosophila |
|
Relations |
Reanalyzed by |
GSM3276693 |
SRA |
SRX124542 |
BioSample |
SAMN00793127 |