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Experiment information
Accession CRX062313
Organism Mus musculus
Title Lung-2-4-IP
BioProject PRJCA001180
BioSample SAMC106545
Platform Illumina HiSeq X Ten
Library
Library name Construction protocol Strategy Source Selection Layout
Total RNA was extracted from tissues using TRIzol reagent (Invitrogen,15596018), followed by DNase I (NEB, M0303L) treatment to remove DNA contamination. Additional phenol-chloroform isolation and ethanol precipitation treatment was performed to remove enzyme contamination. total RNA was fragmented into ~130-nucleotide-long fragments by magnesium RNA fragmentation buffer (NEB, E6150S). The fragmentation was stopped by adding RNA fragmentation stop solution followed by ethanol precipitation. 8ng of fragmented total RNA was used as input and remained RNA was used to do the m6A-seq. The libraries were sequenced on Illumina Hiseq X10 with paired-end 2X 150 bp read length. 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): 130
Release date2019-12-20
Run
Run accession Run data file information
File nameFile size (MB)
CRR072989 CRR072989_f1.fastq.gz
CRR072989_r2.fastq.gz
4,556.31
4,895.04
SubmitterJune Liu (liujune@pku.edu.cn)
OrganizationPeking University
Date submitted2019-09-11