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Sample GSM1406526 Query DataSets for GSM1406526
Status Public on Jun 15, 2014
Title siZNF217_rep1
Sample type SRA
 
Source name MCF7, siZNF217
Organism Homo sapiens
Characteristics cell line: MCF7
cell type: breast cancer
Treatment protocol MCF7 cells were reverse-transfected at a density of 5 x 105 per well in 6-well culture plates. Transfection was performed using 100 nM siRNA targeting ZNF217 (OnTarget plus SMARTpool, Dharmacon, cat # L-004987-01) or non-targeting pool (OnTarget plus non-targeting pool, Dharmacon, cat # D-001810-10) using RNAiMax (Invitrogen) per the manufacturer’s instructions. RNA wascollected at 48h post-transfection.
Growth protocol The MCF7 breast cancer cell line was obtained from American Type Culture Collection and cultured in Dulbecco’s Modified Eagle’s Medium supplemented with 10% fetal bovine serum, 2mM Lglutamine and 1% penicillin/streptomycin.
Extracted molecule total RNA
Extraction protocol RNA samples from triplicate biological replicates of MCF7 cells treated with scrambled siRNA or siZNF217 were extracted using the RNAeasy Kit (Qiagen).
2 ug of RNA samples were processed with the TruSeq RNA Sample Prep Kit (Illumina) to make RNA libraries following the Low-Throughput protocol. Libraries were pooled and sequenced using the HiSeq2500 platform at the UC Davis DNA Technologies Core Facility (http://dnatech.genomecenter.ucdavis.edu).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Data processing fastq files were aligned to the hg19 genome using Tophat 2.0.9 with default parameters. The resulting aligned .bam files were used for cufflinks abundance measurements and cuffdiff differential gene expression anlaysis using the 2.1.1 Cufflinks software.
Genome_build: hg19
Supplementary_files_format_and_content: matrix describing the mean gene transcript abundances and the differential gene expression between siZNF217 and siScramble replicate experiments including statistical measurements of differential expression
 
Submission date Jun 09, 2014
Last update date May 15, 2019
Contact name Seth Frietze
E-mail(s) [email protected]
Phone 8026560569
Organization name University of Vermont
Department BHSC
Street address 106 Carrigan Drive
City Burlington
State/province VT
ZIP/Postal code 05405
Country USA
 
Platform ID GPL11154
Series (1)
GSE58326 Global analysis of ZNF217 chromatin occupancy in the breast cancer cell genome reveals an association with Eralpha
Relations
BioSample SAMN02847877
SRA SRX582010

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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