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Sample GSM2067471 Query DataSets for GSM2067471
Status Public on Oct 06, 2016
Title E12.5 RNA-seq Dup-L∆Bor Rep4
Sample type SRA
 
Source name E12.5 limb buds
Organism Mus musculus
Characteristics genotype: Dup-LdeltaBor
age: E12.5
tissue: limb buds
Extracted molecule polyA RNA
Extraction protocol RNA was extracted from snap-frozen tissue by lysis in Trizol and subsequent purification using the Qiagen RNAeasy Mini Kit
polyA enriched RNA-seq libraries were constructed using the Illumina TruSeq RNA V2 Kit according to manufacturer's instructions
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing RNA-seq reads were mapped to the mouse reference genome (mm9) using the STAR mapper (Dobin et al., 2013) (splice junctions based on RefSeq ;options: ‐‐alignIntronMin 20 ‐‐alignIntronMax 500000 --outFilterMultimapNmax 5 ‐‐outFilterMismatchNmax 10 --outFilterMismatchNoverLmax 0.1).
The uniquely mapped read counts per gene (annotation based on RefSeq genes) were subsequently transformed to FPKM.
Differential Expression was calculated based on the raw read counts per gene via the DEseq2 package (Love et al 2014; default settings).
To create bigwig files coverage profiles were generated by creating a bedgraph file using bedtools genomecov (-ibam —bg split -scale (normalized per million reads)) (bedtools v2.17.0) and then transformed to bigwig files using the bedgraphtobigwig tool from UCSC (http://hgdownload.soe.ucsc.edu/admin/exe/linux.x86_64.v287/bedGraphToBigWig)
Genome_build: mm9
Supplementary_files_format_and_content: bigwig files for normalized RNA-seq profiles
 
Submission date Feb 19, 2016
Last update date May 15, 2019
Contact name Daniel Murad Ibrahim
E-mail(s) ibrahim@molgen.mpg.de, daniel.ibrahim@bih-charite.de
Phone 030 84131516
Organization name Berlin Institute of Health
Department Center for Regenerative Therapies
Street address Augustenburger Platz 1
City Berlin
State/province Berlin
ZIP/Postal code 13353
Country Germany
 
Platform ID GPL17021
Series (2)
GSE78105 Pathogenicity of genomic duplications is determined by formation of novel chromatin domains (neo-TADs) (RNA-seq)
GSE78109 Pathogenicity of genomic duplications is determined by formation of novel chromatin domains (neo-TADs)
Relations
BioSample SAMN04504862
SRA SRX1594182

Supplementary file Size Download File type/resource
GSM2067471_RNAseq-DupLdelBorhom-LB_E125-Rep4.bw 209.8 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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