|
Status |
Public on Jan 27, 2020 |
Title |
4970_2_gNT_UT_R2 |
Sample type |
SRA |
|
|
Source name |
LNCaP_sgNT UT
|
Organism |
Homo sapiens |
Characteristics |
cell line: LNCaP cell type: prostate cancer cell line genotype/variation: control (sgNT) treatment: vehicle for 5 days
|
Treatment protocol |
Cells were plated (500 000 cells / 10cm dish) in RPMI (+10% FBS, +1% pen/strep) at 37C in 5% CO2. Next day, enzalutamide (10 uM) or vehicle was added, and cells were cultured for 5 days (medium was refreshed daily) before harvesting using Trizol.
|
Growth protocol |
LNCaP cells harboring CRISPR constructs were cultured in RPMI (+10% FBS, +1% pen/strep) at 37C in 5% CO2.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA extraction using Trizol Stranded RNA libraries were prepared for sequencing according to Illumina instructions
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
gNT_UT_R2_ATTCCTT
|
Data processing |
Deseq2 was used for RNA-seq data normalization. The differential expression was based on the ratio of normalized read counts (FPKM, after library size correction). An absolute fold-change threshold of 2 was used. Genes with a coverage <50 in both conditions were excluded from the analyses to prevent spurious results. Genome_build: hg38 Supplementary_files_format_and_content: readcountfiles: tab-separated gene counts and gene annotation for all samples
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|
|
Submission date |
Apr 24, 2019 |
Last update date |
Jan 27, 2020 |
Contact name |
Sander Palit |
E-mail(s) |
[email protected]
|
Organization name |
Netherlands Cancer Institute
|
Street address |
Plesmanlaan 121
|
City |
Amsterdam |
ZIP/Postal code |
1066 CX |
Country |
Netherlands |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE130246 |
RNA-seq control (sgNT) and TLE3KO (sgTLE3) cells treated with 10 uM enzalutamide or vehicle |
|
Relations |
BioSample |
SAMN11490484 |
SRA |
SRX5729230 |