|Public on Sep 28, 2015
|Original Bone Marrow RNA
|sample type: pure bone marrow RNA (BMO)
|Samples used in the study are commercially available RNAs derived from mixture of multiple cell lines and RNAs extracted from patient bone marrow specimens
|100 ng of starting RNAs were amplified with Ambion WT-plus amplification kit and 5,000 ng of biotin-labeled cDNAs were hybridized.
|Labeled cDNAs were hybridized onto Affymetrix Human Transcriptome Arrays v2.0 (HTA2.0) following Affymetrix standard protocols.
|Array scanning was performed according to the manufacturer's instruction (Affymetrix).
|Raw data were processed with the Expression Console (Affymetrix) for background correction and normalization, and both probeset (exon) and gene (transcript cluster) level data were generated.
|Mar 06, 2015
|Last update date
|Sep 28, 2015
|Washington University School of Medicine
|660 S. Euclid Ave.
|Multi-platform assessment of transcriptional profiling technologies utilizing a precise probe mapping methodology (Affymetrix_HTA2.0)
|Multi-platform assessment of transcriptional profiling technologies utilizing a precise probe mapping methodology
|GSM1627008 (gene-level analysis)