GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM98571 Query DataSets for GSM98571
Status Public on Mar 20, 2006
Title ES 10pg amplified, technical rep4
Sample type RNA
Source name Total RNA from Embryonic Stem cell culture diluted to 10 pg
Organism Mus musculus
Characteristics Line: E14tg2a
Extracted molecule total RNA
Extraction protocol The total RNA was prepared by the RNeasy Mini Kit (Qiagen) according to the manufacturer's instruction
Label biotin
Label protocol Biotinylated cRNA were prepared from the PCR-amplified double-starnded cDNA according to the standard Affymetrix protocol (Affymetrix GeneChip Expression Analysis Technical Manual, 2004, Affymetrix: Eukaryotic One-Cycle Target Labeling Assay)
Hybridization protocol Hybridization was performed according to the standard Affymetrix protocol (Affymetrix GeneChip Expression Analysis Technical Manual, 2004, Affymetrix: Eukaryotic Target Hybridization)
Scan protocol The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix)
Description Gene expression data to verify the PCR-based single-cell cDNA amplification method (the V1V3 method)
Data processing CEL data were generated by GeneChip Operating Software and then subjected to the dCHIP software. Data obtained from the eight amplified samples (ES-10pg-amplified-rep1:8) were normalized together with the default settings. The Model-Based Expression Indices (MBEI) were calculated using the PM/MM difference mode with log-2 transformation of signal intensity and truncation of low values to zero.
Submission date Feb 27, 2006
Last update date Aug 28, 2018
Contact name Kazuki Kurimoto
Organization name Kyoto University
Department Graduate school of medicine
Lab Department of anatomy and cell biology
Street address Yoshida-Konoe-cho, Sakyo-ku
City Kyoto
ZIP/Postal code 606-8501
Country Japan
Platform ID GPL1261
Series (2)
GSE4308 Expression data for validation of single cell cDNA amplification method (V1V3 method)
GSE4309 An improved single-cell cDNA amplification method for efficient high-density oligonucleotide microarray analysis
Reanalyzed by GSE119085

Data table header descriptions
VALUE Model-based Expression Index calculated with dCHIP
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)

Data table
AFFX-TrpnX-M_at 25.59925642 A
AFFX-TrpnX-5_at 16.89377691 A
AFFX-TrpnX-3_at 33.69400458 A
AFFX-TransRecMur/X57349_M_at 95.5113315 A
AFFX-TransRecMur/X57349_5_at 23.70566566 A
AFFX-TransRecMur/X57349_3_at 63.83563057 A
AFFX-ThrX-M_at 18.78227611 A
AFFX-ThrX-5_at 18.64077581 A
AFFX-ThrX-3_at 1 A
AFFX-r2-P1-cre-5_at 9358.100454 P
AFFX-r2-P1-cre-3_at 11368.07218 P
AFFX-r2-Ec-bioD-5_at 3168.754114 P
AFFX-r2-Ec-bioD-3_at 3176.671075 P
AFFX-r2-Ec-bioC-5_at 542.6920634 P
AFFX-r2-Ec-bioC-3_at 888.7784338 P
AFFX-r2-Ec-bioB-M_at 342.8491179 P
AFFX-r2-Ec-bioB-5_at 321.8021155 P
AFFX-r2-Ec-bioB-3_at 293.4477833 P
AFFX-r2-Bs-thr-M_s_at 19.18956363 A
AFFX-r2-Bs-thr-5_s_at 4.919050956 A

Total number of rows: 45101

Table truncated, full table size 1084 Kbytes.

Supplementary file Size Download File type/resource
GSM98571.CEL.gz 5.9 Mb (ftp)(http) CEL
Raw data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap