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Sample GSM4509253 Query DataSets for GSM4509253
Status Public on Jun 19, 2020
Title con-2
Sample type SRA
 
Source name PK-15 cell line
Organism Sus scrofa
Characteristics cell line: PK-15
cell type: Kidney cell line
infection: Mock
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using the Mini Best Universal RNA Extraction kit (Takara, Dalian, China).
rRNAs were depleted with RNA sample purification beads, which employ an RNaseH-based method. Then, the RNA was fragmented and reverse transcribed. The cDNA library was subjected to end repair, poly(A)-tailing, adaptor ligation, and PCR amplification of 12–15 cycles for sequencing library construction.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model HiSeq X Ten
 
Description Negative Control
processed data file: Normalized dataset.xls
Data processing Reads were trimmed to remove the bases with low quality and adapter sequences.
The trimmed reads were aligned to the pig reference genome using Hisat2.
Gene expression levels were quantified using the featureCounts.
Differentially expressed genes between NC and PCV2 infection group were selected by DESeq2 with Padj. <0.05 and fold change (FC) of >1.2 or <0.0.83.
Genome_build: Sscrofa11.1
Supplementary_files_format_and_content: Normalized dataset.xls: Excel file includes FPKM for each sample.
 
Submission date May 01, 2020
Last update date Jun 19, 2020
Contact name Jin He
E-mail(s) hejin@zju.edu.cn
Organization name Zhejiang University
Street address Yuhangtang Road No.866
City Hangzhou
ZIP/Postal code 310058
Country China
 
Platform ID GPL22918
Series (1)
GSE149711 Identification of lncRNAs involved in the PCV2 infection of PK-15 cells
Relations
BioSample SAMN14790162
SRA SRX8241343

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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