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Sample GSM4667087 Query DataSets for GSM4667087
Status Public on Jul 11, 2020
Title 3MK9
Sample type SRA
 
Source name kidney
Organism Mus musculus
Characteristics strain: C57BL/6
tissue: kidney
Sex: male
age: 3 month old
Growth protocol The mice were housed at 25°C and fed standard rodent chow and tap water.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol reagent (Invitrogen, CA, USA) following the manufacturer’s procedure. The total RNA quantity and purity were analysis of Aglient 2100 Bioanalyzer and RNA 6000 Nano LabChip Kit (Agilent, CA, USA) with RIN number >7.0.
Approximately 10 ug of total RNA was used to deplete ribosomal RNA according to the manuscript of the Ribo-Zero™ rRNA removal kit (Illumina, San Diego, USA).Then the left RNA was fragmented into small pieces using divalent cations under elevated temperature. The cleaved RNA fragments were reverse-transcribed to create the final cDNA library in accordance with the protocol for the Truseq Stranded Total RNA HT Sample Prep Kit (Illumina, San Diego, USA).
 
Library strategy ncRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina HiSeq 4000
 
Data processing Illumina Casava1.8 software used for basecalling.
Prior to assembly, the low quality reads(1,reads containing sequencing adaptors; 2,reads containing sequencing primer;3, nucleotide with q quality score lower than 20) were removed.
We aligned reads of samples to the reference genome using TopHat2 package.
The mapped reads of each sample were assembled using StringTie, all transcriptomes were merged to reconstruct a comprehensive transcriptome.
Unmapped reads were still mapped to genome using tophat-fusion. CIRCExplorer2 was used to denovo assemble the mapped reads to circular RNAs at first; Then, back splicing reads were identified in unmapped reads by tophat-fusion and CIRCExplorer2. All samples were generated unique circular RNAs.
Genome_build: Mus_musculus Ensembl relaese-88
Supplementary_files_format_and_content: tab-delimited text files include FPKM values for each isoforms
 
Submission date Jul 10, 2020
Last update date Jul 11, 2020
Contact name Fan Fan Gao
E-mail(s) [email protected]
Phone 15891722241
Organization name the First Affiliated Hospital of Xi’an Jiaotong University
Department Dialysis Department of Nephrology Hospital
Lab Dialysis Department of Nephrology Hospital
Street address West Yanta Road 277
City Xi’an
State/province Shaanxi
ZIP/Postal code 710061
Country China
 
Platform ID GPL21103
Series (2)
GSE154220 Whole transcriptome analysis for kidney aging in mice [non-coding RNA]
GSE154223 Whole transcriptome analysis for kidney aging in mice
Relations
BioSample SAMN15504560
SRA SRX8707945

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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