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Status |
Public on Nov 01, 2018 |
Title |
SR4 |
Sample type |
SRA |
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Source name |
Spleen
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Organism |
Sus scrofa |
Characteristics |
breed: Y x L age: 7-day old infection: Clostridium perfringens type C group: SR tissue: spleen
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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
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 4000 |
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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
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Submission date |
Oct 23, 2017 |
Last update date |
May 15, 2019 |
Contact name |
y zun qiang |
E-mail(s) |
756707388@qq.com
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Phone |
18719823101
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Organization name |
College of Animal Science and Technology
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Street address |
No. 1 Yingmen village, Anning District
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City |
Lanzhou |
State/province |
Gansu Province |
ZIP/Postal code |
730070 |
Country |
China |
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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 |
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Relations |
BioSample |
SAMN07822592 |
SRA |
SRX3313031 |
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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