|
Status |
Public on Dec 01, 2018 |
Title |
STAT-upd-rep2 |
Sample type |
SRA |
|
|
Source name |
S2R+ cell line with STAT492E knocked out using CRISPR
|
Organism |
Drosophila melanogaster |
Characteristics |
genotype/variation: STAT92E mutant treatment: upd ligand treated cell line: STAT492E
|
Treatment protocol |
upd or control media was added for 1 hour
|
Growth protocol |
Cells were treated with upd or control media for 1 hour before RNA extraction
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using Trizol reagent RNA-seq library preparation was performed on total RNA by poly-A selection using the Wafergen PrepX RNA-Seq Library Kit for Illumina and the Apollo 343 NGS Library Prep System (Wafergen)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
STAT92E mutant cells
|
Data processing |
Sequenced reads were trimmed with Trimmomatic version 0.36, mapped to Drosophila genome (dmel_r6.24) with STAR version 2.5.2b. Gene counts were normalized by the gene length of the longest isoform annotated at dmel_r6.24 into RPKM. Genome_build: dm6.24
|
|
|
Submission date |
Nov 30, 2018 |
Last update date |
Dec 03, 2018 |
Contact name |
Yanhui Hu |
E-mail(s) |
[email protected]
|
Phone |
617-432-6546
|
Organization name |
Harvard Medical School
|
Department |
Genetics
|
Lab |
Norbert Perrimon
|
Street address |
77 Avenue Louis Pasteur
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
|
|
Platform ID |
GPL19132 |
Series (1) |
GSE123167 |
Targets of JAK STAT signaling in Drosophila cells |
|
Relations |
BioSample |
SAMN10504979 |
SRA |
SRX5084354 |