|
Status |
Public on Dec 31, 2021 |
Title |
SF268_GCN2cr3_N675_3D_R1 |
Sample type |
SRA |
|
|
Source name |
Glioblastoma
|
Organism |
Homo sapiens |
Characteristics |
cell line: SF268 treatment: neratinib 675 nM timepoint: 72 hr
|
Treatment protocol |
Inhibitors or DMSO were added to the cultured cells and treated for indicated times.
|
Growth protocol |
Cells were cultured in DMEM + 10% FBS
|
Extracted molecule |
total RNA |
Extraction protocol |
CRISPR screen sequencing libraries were made with nested PCRs of the sgRNA region.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to the TKOv3 library sequences with bowtie. Sequenced reads aligned to GRCh38 with salmon. Differential expression analysis was performed with DESeq2. Genome_build: GRCh38 Supplementary_files_format_and_content: tab delimited .txt file
|
|
|
Submission date |
Nov 16, 2021 |
Last update date |
Dec 31, 2021 |
Contact name |
Colin Tang |
E-mail(s) |
[email protected]
|
Organization name |
Weill Cornell Medicine
|
Street address |
1300 York Ave.
|
City |
New York |
State/province |
NY |
ZIP/Postal code |
10065 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE188958 |
GCN2 kinase Activation by ATP-competitive Kinase Inhibitors |
|
Relations |
BioSample |
SAMN23195527 |
SRA |
SRX13150050 |