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Sample GSM2843909 Query DataSets for GSM2843909
Status Public on Dec 04, 2018
Title Mettl3KO_Input
Sample type SRA
 
Source name ES cells
Organism Mus musculus
Characteristics background: Rosa26:CRE, Bir ligase
cell type: ES cells
genotype: Mettl3KO
rip antibody: none
Growth protocol All samples: Mouse embryonic stem cells were cultured on gelatin-coated dishes in mES medium (DMEM (Gibco 21969-035), supplemented with 15% fetal bovine serum (Gibco), 1x non-essential amino acids (Gibco), 1mM sodium pyruvate (Gibco), 2 mM L-glutamine (Gibco), 0.1mM 2-mercaptoethanol (Sigma), 50mg/ml penicillin, 80mg/ml streptomycin and LIF conditioned medium) at 37°C in 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA from mESCs was isolated using Absolutely RNA Microprep Kit (Stratagene), followed by mRNA selection using double Oligo d(T)23 (NEB) purification.
Libraries were prepared with 30 ng of m6A-IPs and duplicate input samples (200ng mRNA) using NEB-Next RNA Directional Library Preparation Kit
 
Library strategy RIP-Seq
Library source transcriptomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Data processing Reads were aligned to the mm10 mouse genome assembly using Bowtie with the parameters ‘-m 1 --best --strata’. SAM files were converted to BAM format, sorted and indexed using SAMtools.
MACS2 was used to call peaks of m6A enrichment for WT IP vs input samples, using the default parameters.
BigWig files for each sample were created using the qExportWig function from the QuasR package in R (Gaidatzis et al. 2014) with 50-bp bins.
Genome_build: mm10
Supplementary_files_format_and_content: bigWig: scores represent normalized counts in 50-bp bins. narrowPeak: BED6+4 format representing peak locations. Columns 5-10 are defined by MACS2 (https://github.com/taoliu/MACS).
 
Submission date Nov 07, 2017
Last update date May 15, 2019
Contact name Jean-Yves Roignant
Organization name Institute of molecular Biology
Lab Roignant
Street address Ackermannweg 4
City Mainz
ZIP/Postal code 55128
Country Germany
 
Platform ID GPL17021
Series (2)
GSE106613 Zc3h13/Flacc is required for adenosine methylation by bridging the mRNA binding factor Rbm15/Spenito to other components of the m6A machinery
GSE106614 Zc3h13/Flacc is required for adenosine methylation by bridging the mRNA binding factor Rbm15/Spenito to other components of the m6A machinery
Relations
BioSample SAMN07987882
SRA SRX3369946

Supplementary file Size Download File type/resource
GSM2843909_Mettl3KO_input.bw 25.3 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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