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Sample GSM1295053 Query DataSets for GSM1295053
Status Public on Nov 17, 2014
Title CJ7 wt RNA
Sample type SRA
 
Source name ES cells
Organism Mus musculus
Characteristics cell line: CJ7
cell type: ES cells
background: 129/S
Growth protocol ESCs were plated with irradiated murine embryonic fibroblasts (MEFs) and grown under typical ESC conditions on gelatinized tissue culture plates. Briefly, cells were grown in Knockout DMEM supplemented with 15% fetal bovine serum, leukemia inhibitory factor (LIF), non-essential amino acids, L-glutamine, and penicillin/streptomycin as previously described (Boyer et al., 2006). Before collection or in vitro differentiation, cells were briefly plated on non-gelatinized tissue culture plates to remove MEFs.
Extracted molecule total RNA
Extraction protocol RNA was isolated using Trizol according to manufacturer’s instructions, including optional step in protocol. RNA quality was determined by Agilent Bioanalyzer. RNA-seq libraries were prepared as previously described (Wamstad et al., 2012). A final round of size selection by Agencourt AMPure XP beads was performed to remove small fragments such as primers. Sequencing was run on either an Illumina GA-2 or Hi-Seq (barcoded). .
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description prepared and sequenced with ST20; use as wt control for batch normalization.
Data processing Illumina Offline BaseCaller1.9.3 software used for basecalling.
Bowtie v. 0.12.7, Tophat v1.3.2 and Cufflinks v 1.2.1 and Cuffdiff were utilized to determine the expression levels of genes (Trapnell et al., 2012), using a NCBIN37, ENSEMBL-based annotation and flags -p 4, -r 170, --segment-length 20 --segment-mismatches 1 --solexa1.3-quals --no-novel-juncs
Cufflinks was guided using the same annotation as Tophat with flags -b -u -p 6
Genome_build: mm9 (iGenome)
Supplementary_files_format_and_content: Txt file containing a table of RPKM values for each sample described in the study
 
Submission date Dec 19, 2013
Last update date May 15, 2019
Contact name Laurie A Boyer
E-mail(s) lboyer@mit.edu
Phone 617 324-3335
Organization name Massachusetts Institute of Technology
Department Biology
Lab Boyer
Street address 77 Massachusetts Avenue
City Cambridge
State/province MA
ZIP/Postal code 02139
Country USA
 
Platform ID GPL13112
Series (2)
GSE53506 PRC2 coordinates lineage fidelity and DNA methylation during ESC differentiation (RNA-Seq)
GSE53508 PRC2 coordinates lineage fidelity and DNA methylation during ESC differentiation
Relations
BioSample SAMN02469230
SRA SRX396329

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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