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Sample GSM3021901 Query DataSets for GSM3021901
Status Public on Apr 09, 2018
Title MDS1195_tMDS_RNA-seq
Sample type SRA
 
Source name Hematopoietic stem cells
Organism Homo sapiens
Characteristics cell type: CD34+ hematopoietic stem cells
disease status: Myelodysplastic syndrome
myelodysplastic syndrome stage: tMDS
Extracted molecule total RNA
Extraction protocol RNA was extracted using the RNeasy kit (Qiagen, Valencia, CA) from magnetic bead affinity-enriched CD34+ cells (>90%) obtained from marrow aspirates (Miltenyi Biotec, Auburn, CA). The samples were snap frozen in liquid nitrogen and stored at -80oC on the day of collection. Quality check was performed by Bioanalyzer2100 (Agilent Technologies, Palo Alto, CA) using High Sensitivity RNA Chips.
5-10ng of total RNA (RIN>7) was amplified by using the SMARTer Ultra Low RNA Kit for Illumina Sequencing (Clontech Laboratories, Inc., Mountain View, CA) after testing for the fidelity of the protocol on HeLa cell derived RNA (Supplementary Methods, Suppl Figure 1 of publication). cDNA library synthesis and sequencing were performed as previously described (See Supplementary Methods of publication). The libraries were sequenced on the Illumina HiSeq 2000 platform at the Stanford Sequencing Center.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description MDS_40
processed data file: MDS_genes_edgeR.txt
processed data file: MDS_isoform_fpkm.txt
Data processing Illumina Casava1.7 software used for basecalling.
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to hg19 whole genome using STAR or TopHat2.
Fragments Per Kilobase of exon per Megabase of library size (FPKM) were calculated using a protocol from Trapnell C et al. Read Counts (cpm) were generated using EdgeR package.
Genome_build: hg19 (GRCh37)
Supplementary_files_format_and_content: MDS_isoform_fpkm.txt: Combined matrix of normalized abundance measurement - isoform expression (fpkm) using CuffDiff2.
Supplementary_files_format_and_content: MDS_genes_edgeR.txt: Combined matrix of normalized abundance measurement - gene expression (counts) using EdgeR.
 
Submission date Feb 25, 2018
Last update date Apr 09, 2018
Contact name Varsha Rao
E-mail(s) varshar@stanford.edu
Phone 6507245777
Organization name Stanford University
Department Genetics
Lab Snyder Lab
Street address 300 Pasteur Drive
City Stanford
State/province California
ZIP/Postal code 94305
Country USA
 
Platform ID GPL11154
Series (1)
GSE111085 Distinct Transcriptomic and Exomic Abnormalities within Myelodysplastic Syndrome Marrow Cells
Relations
BioSample SAMN08605752
SRA SRX3741171

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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