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Sample GSM3734465 Query DataSets for GSM3734465
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
 
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

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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