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Status |
Public on Sep 30, 2013 |
Title |
marrow CD3 T cells_post_NR1 (nonresponder) |
Sample type |
RNA |
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Source name |
marrow derived CD3+ T cells, after DLI
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Organism |
Homo sapiens |
Characteristics |
patient: nonresponder cell type: bone marrow-derived CD3+ T cells patient: nonresponder cell type: bone marrow-derived CD3+ T cells
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Treatment protocol |
BMMCs from DLI responders and nonresponders were thawed, and CD3+ T cells were enriched using magnetic bead sorting (Miltenyi Biotec).
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
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Label |
biotin
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Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
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Hybridization protocol |
Total RNA was amplified followed by cDNA synthesis (Ovation Pico WTA System V2, NuGEN, San Carlos, CA) and samples were hybridized to Affymetrix U133A+ 2.0 arrays (Santa Cruz, CA) at the DFCI Microarray Core Facility
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Scan protocol |
GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
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Description |
Gene expression data from marrow derived CD3+ T cells in non-responder (NR1) after DLI
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Data processing |
The data were analyzed using Robust Multichip Average (RMA) as in implemented in the R package affy. Probe level data were averaged to the gene level, and the resulting values were converted to a log2 scale for downstream analysis.
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Submission date |
Jul 21, 2013 |
Last update date |
Sep 30, 2013 |
Contact name |
Pavan Bachireddy |
E-mail(s) |
[email protected]
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Organization name |
Dana-Farber Cancer Institute
|
Lab |
Catherine Wu, MD
|
Street address |
77 Avenue Louis Pasteur
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
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|
Platform ID |
GPL571 |
Series (1) |
GSE49067 |
Expression data from responders/nonresponders before/after receiving DLI for relapse of CML s/p BMT |
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