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Sample GSM1306495 Query DataSets for GSM1306495
Status Public on Jan 15, 2014
Title MCF7 mRNAseq library
Sample type SRA
 
Source name MCF7 cell culture
Organism Homo sapiens
Characteristics cell line: MCF7
purification: oligo(dT) beads
Growth protocol MCF-7 cells were grown in D-MEM high glucose with 10% (v/v) fetal bovine serum, 1% (v/v) 2 mM L-glutamine, 1% (v/v) 10,000 U/ml penicillin/10,000 µg/ml streptomycin.
Extracted molecule total RNA
Extraction protocol oligodT-purified RNA converted into cDNA by TruSeq™ RNA Sample Preparation Kit
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Read demultiplexing, read filtering and adapter trimming was done using flexbar (Dodt et al, 2012).
We used TopHat2 (version 2.06) (Trapnell et al., 2009 and Kim et al. 2013) for spliced alignment of reads to the human reference genome sequence (hg18).
We used Cuffdiff (version 2.0.2)(Trapnell et al., 2010) to generate FPKM values
Genome_build: hg18
Supplementary_files_format_and_content: FPKM table
 
Submission date Jan 14, 2014
Last update date May 15, 2019
Contact name Markus Landthaler
E-mail(s) markus.landthaler@mdc-berlin.de
Phone +49-30-9406-3026
Organization name Max-Delbrück-Center for Molecular Medicine
Department Berlin Institute for Medical Systems Biology
Street address Robert-Rössle-Straße 10
City Berlin
ZIP/Postal code 13125
Country Germany
 
Platform ID GPL16791
Series (1)
GSE49831 Differential Protein Occupancy Profiling of the mRNA Transcriptome
Relations
BioSample SAMN02584019
SRA SRX426377

Supplementary file Size Download File type/resource
GSM1306495_MCF7_mRNAseq_FPKM.txt.gz 254.5 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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