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Sample GSM2828339 Query DataSets for GSM2828339
Status Public on Nov 01, 2018
Title SR3
Sample type SRA
 
Source name Spleen
Organism Sus scrofa
Characteristics breed: Y x L
age: 7-day old
infection: Clostridium perfringens type C
group: SR
tissue: spleen
Extracted molecule total RNA
Extraction protocol Spleen were removed, flash frozen and total RNA was extracted from each sample using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).
RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 4000
 
Data processing Fastq format raw reads (raw data) were handled through in-house perl scripts. Clean reads (clean data) were gained by removing adapters, ploy-N and low quality reads from raw reads (raw data). Meanwhile, Q20, Q30 and GC content of the clean data were evaluated. The paired-end clean reads were mapped to the pig genome sequence assembly (Sscrofa 10.2) with Tophat (v2.0.9) software.
CNCI, CPC, PFAM and phyloCSF, were used to obtain the candidate lncRNA. Firstly, transcripts without coding potential were achieved using any of the four tools with earlier described instructions. Next, those without coding potential shared by four tools were screened as the candidate lncRNAs for subsequent research.
The genes expression level of both lncRNAs and protein-coding in each sample was calculated by FPKM (fragments per kb for a million reads) evaluated using Cuffdiff (v2.1.1)
To explore transcripts conservation, the Phast (v1.3) software was widely used for phylogenetic analysis and thus phastCons expression.
Gene Ontology (GO) enrichment analysis of differentially expressed genes or lncRNA target genes were implemented by the GOseq R package. KOBAS software was performed to test the statistical enrichment of differential expression genes or lncRNA target genes in KEGG pathways.
Coding genes 10k/100k upstream and downstream of lncRNA were treated as the cis target gene. Then, the trans role of lncRNA is to identify using the expression level.
Genome_build: Sus scrofa 10.2
Supplementary_files_format_and_content: Tab-delimited text file includes FPKM values for each Sample
 
Submission date Oct 23, 2017
Last update date May 15, 2019
Contact name y zun qiang
E-mail(s) 756707388@qq.com
Phone 18719823101
Organization name College of Animal Science and Technology
Street address No. 1 Yingmen village, Anning District
City Lanzhou
State/province Gansu Province
ZIP/Postal code 730070
Country China
 
Platform ID GPL22475
Series (1)
GSE105797 Analyses of long non-coding RNA and mRNA profiling in the spleen of diarrhea piglets caused by Clostridium perfringens type C
Relations
BioSample SAMN07822589
SRA SRX3313030

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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