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Status |
Public on Jun 19, 2020 |
Title |
con-2 |
Sample type |
SRA |
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Source name |
PK-15 cell line
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Organism |
Sus scrofa |
Characteristics |
cell line: PK-15 cell type: Kidney cell line infection: Mock
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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.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
HiSeq X Ten |
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Description |
Negative Control processed data file: Normalized dataset.xls
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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.
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Submission date |
May 01, 2020 |
Last update date |
Jun 19, 2020 |
Contact name |
Jin He |
E-mail(s) |
hejin@zju.edu.cn
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Organization name |
Zhejiang University
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Street address |
Yuhangtang Road No.866
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City |
Hangzhou |
ZIP/Postal code |
310058 |
Country |
China |
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Platform ID |
GPL22918 |
Series (1) |
GSE149711 |
Identification of lncRNAs involved in the PCV2 infection of PK-15 cells |
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Relations |
BioSample |
SAMN14790162 |
SRA |
SRX8241343 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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