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Experiment information
Accession CRX307004
Organism Capra hircus
Title D4501
BioProject PRJCA007633
BioSample SAMC539143
Platform Illumina HiSeq 2000
Library
Library name Construction protocol Strategy Source Selection Layout
The total RNA of samples was extracted using RNeasy Plus Universal Mini Kit (QIAGEN, Germany). A total amount of 2 µg RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using VAHTS mRNA-seq v2 Library Prep Kit for Illumina were added to attribute sequences to each sample. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads. Fragmentation was carried out using fragmentation buffer. First strand cDNA was synthesized and second strand cDNA synthesis was subsequently performed. Remaining overhangs were converted into blunt ends. After adenylation of 3’ ends of DNA fragments, adaptor with hairpin loop structure were ligated. Then the PCR was performed. At last, Qubit HS quantification, Agilent 2100 Bioanalyzer/Fragment Analyzer 5300 quality control, the final library size of about 350bp. RNA-Seq TRANSCRIPTOMIC PCR PAIRED
Processing Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
Insert size (bp): 400
Release date2021-12-29
Run
Run accession Run data file information
File nameFile size (MB)
CRR356440 CRR356440_f1.fastq.gz
CRR356440_r2.fastq.gz
2,365.6
2,956.81
SubmitterYue Liu (liuyue196160@163.com)
OrganizationInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences
Date submitted2021-12-23