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Sample GSM3239381 Query DataSets for GSM3239381
Status Public on Jan 21, 2019
Title Mm_WT_PKHneg_msphr_L-MycER_rna_rep2
Sample type SRA
 
Source name Mammosphere culture
Organism Mus musculus
Characteristics strain: FVB/Hsd
tissue: normal mammary gland
age: 7 weeks old
genotype: wild type
infection: infected with L-pWPI-MycER
treatment: FACS sorted for PKH negative
passage: M3 (72 hours after plating)
Growth protocol cells were isolated from mammary tissue derived from WT or transgenic mice and plated in anchorage independent condition (polyHEMA coated plates) to form mammospheres. Mammospheres were serially passaged in STEM Medium (serum-free mammary epithelial basal medium MEBM, supplemented with 2 mM glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin, 5 μg/ml insulin, 0.5 μg/ml hydrocortisone, 2% B27, 20 ng/ml EGF and βFGF and 4 μg/ml heparin). Mammospheres were disaggregated and RNA extracted.
Extracted molecule polyA RNA
Extraction protocol RNA from mammospheres was extracted with Maxwell® 16 LEV simplyRNA cells kit (Promega) and reverse transcribed using random primers and ImProm-II™ reverse transcriptase (Promega), following manufacturer’s instructions.
Libraries of template RNA molecules were prepared from 0.5 to 2 μg high quality input RNA using the Illumina® TruSeq® RNA Sample Preparation Kit v2, following manufacturer’s instructions.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Data processing Basecalls performed using CASAVA version 1.9
Data were filtered using the Illumina quality control flag
Reads were aligned to the mus musculs genome build mm10 using tophat (v2.0.8), which uses Bowtie (2.1.0) and Samtools (v0.1.18) using default parameters and --transcriptome Mus Musculus index, UCSC mm10 gtf.
Raw read counts were summarised using HTSeq (v0.5.3p9), then normalized for library size differences using estimateSizeFactors function from DESeq2 package (v1.10.1).
Genome_build: mm10
Supplementary_files_format_and_content: tab-delimited text files include normalized expression value, log2fold change, pvalue and adjusted pvalue for each gene for each DE analysis
 
Submission date Jun 29, 2018
Last update date Jan 21, 2019
Contact name Pier Giuseppe Pelicci
Organization name European Institute of Oncology
Department Department of Experimental Oncology
Street address Via Adamello, 16
City Milano
ZIP/Postal code 20139
Country Italy
 
Platform ID GPL13112
Series (2)
GSE87003 Myc activation in breast cancer is due to p53-loss and sustains self-renewal of cancer stem cells (RNA-Seq)
GSE87004 Myc activation in breast cancer is due to p53-loss and sustains self-renewal of cancer stem cells
Relations
BioSample SAMN09530282
SRA SRX4328947

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

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