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Sample GSM3656420 Query DataSets for GSM3656420
Status Public on Oct 04, 2019
Title hiPSC, biological replicate-1
Sample type RNA
 
Source name human induced pluripotent stem cells
Organism Homo sapiens
Characteristics cell line: hiPSC line GM25256*B
cell type: induced pluripotent stem cells
differentiation stage: Initial
Treatment protocol None
Growth protocol The hiPSC line GM25256*B was induced to differentiate into human Leydig cell-like cells (hLLCs) and human adrenal cell-like cells (hALCs), respectively.
Extracted molecule total RNA
Extraction protocol Total RNA samples were prepared using Ambion® RiboPure™ Kit (Thermofisher Scientific, AM1924), according to the manufacture's instructions.
Label biotin
Label protocol After validation of the RNA quality with Bioanalyzer 2100, The standard Affymetrix WT plus protocol was used to generate cDNA from 250 ng total RNA. First and second strand cRNA synthesis was according to the manufacturer’s instructions. ss-cDNA synthesis was followed by 15ug of cRNA in vitro transcription and a second round of ss-cDNA synthesis according to the manufacturer’s instructions. Fragmentation of 5.5ug of single-stranded cDNA was performed using the Affymetrix GeneChip WT Terminal Labeling and Hybridization protocol per the manufacturer's instructions Reagent Kit (Affymetrix).
 
Hybridization protocol Following fragmentation and Labeling samples were hybridized for at 60 RPM for 16 hrs at 45C on Clariom™ S Assay, human array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 4G.
Description Gene expression data from hiPSCs
Data processing The data were preprocessed and analyzing using Partek Genomic Suite.
Probe level data were summarized using the RMA. Background are adjusted using RMA background correction. Quantile normalization was used to correct for array bias. All probe level intensities were log 2 transformed. Probesets were summarized using median polish.
 
Submission date Mar 06, 2019
Last update date Oct 04, 2019
Contact name Lu Li
E-mail(s) greenpearll0804@gmail.com
Phone 323-442-0277
Organization name University of Southern California
Department School of Pharmacy
Street address Room 706, 1985 Zonal Ave
City Los Angeles
State/province CA
ZIP/Postal code 90089
Country USA
 
Platform ID GPL23159
Series (1)
GSE127915 Transcriptome Profiling for human Leydig cell-like cells, adrenal cell-like cells, and induced pluripotent stem cells

Data table header descriptions
ID_REF
VALUE log2 normalized signal

Data table
ID_REF VALUE
TC0100006437.hg.1 5.70523
TC0100006476.hg.1 7.33362
TC0100006479.hg.1 8.08828
TC0100006480.hg.1 6.64708
TC0100006483.hg.1 6.83599
TC0100006486.hg.1 8.03811
TC0100006490.hg.1 5.25179
TC0100006492.hg.1 6.63202
TC0100006494.hg.1 7.06603
TC0100006497.hg.1 6.82317
TC0100006499.hg.1 7.44693
TC0100006501.hg.1 6.97396
TC0100006502.hg.1 5.41563
TC0100006514.hg.1 6.37647
TC0100006516.hg.1 7.58351
TC0100006517.hg.1 5.93225
TC0100006524.hg.1 6.46104
TC0100006540.hg.1 5.68183
TC0100006548.hg.1 4.63169
TC0100006550.hg.1 8.3985

Total number of rows: 21448

Table truncated, full table size 545 Kbytes.




Supplementary file Size Download File type/resource
GSM3656420_AN598_Sample7_Control_Clariom_S_Human_.CEL.gz 1.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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