|
Status |
Public on Apr 27, 2020 |
Title |
shMOB2 |
Sample type |
SRA |
|
|
Source name |
LN-229 cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: epithelial glioma cells passages: 15-18 tissue: brain
|
Treatment protocol |
LN-229 cells were infected with pGIPZ-CTRL and MOB2-shRNA lentiviruses, and stable clones were selected using puromycin.
|
Growth protocol |
Cells were routinely generated by re-plating with DMEM supplied with 5% FBS.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was isolated from LN-229-shMOB2 or LN-229-shControl cells using TRIzol Reagent. The sequencing libraries were prepared using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) according to the manufacturer's instructions.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
clean reads were retained by removing reads containing adapter, reads containing ploy-N and low quality reads from raw fastq data using in-house perl scripts RNASeq reads were aligned to the hg38 genome assembly using Hisat2 v2.0.5 featureCounts v1.5.0-p3 was used to generate gene-level count matrix as input for edgeR’s statistical model Differential expression analysis between shFKBP9 and shControl cells was performed using the edgeR package Genome_build: hg38 Supplementary_files_format_and_content: Excel file include FPKM expression value and gene annotation
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|
|
Submission date |
Oct 24, 2019 |
Last update date |
Apr 27, 2020 |
Contact name |
Ke Jiang |
Organization name |
Dalian Medical University
|
Street address |
lvshun south road no.9
|
City |
Dalian |
State/province |
Liaoning |
ZIP/Postal code |
116044 |
Country |
China |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE139339 |
RNA sequencing analysis of LN-229-shControl and LN-229-shMOB2 cells |
|
Relations |
BioSample |
SAMN13108587 |
SRA |
SRX7052198 |