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Status |
Public on Nov 21, 2014 |
Title |
100_spiked_MCF7_a |
Sample type |
RNA |
|
|
Source name |
breast cancer
|
Organism |
Homo sapiens |
Characteristics |
experiment: 1 sample type: spiked cells cell line: MCF7 cell number 5ml: 100 donor: d1 replicate: a tissue: blood
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extraction was performed according to the manufacturer’s instructions and RNA was eluted in 5 or 10 ul of RNase-free water (Ambion), depending on the experimental setting.
|
Label |
Cy3
|
Label protocol |
Flourescently labeled cRNA were prepared according to the standard Illumina protocol.
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|
|
Hybridization protocol |
cRNA were hybridazed onto Illumina HumanHT-12 WG-DASL V4.0 R2 expression beadchip according to the standard Illumina protocol.
|
Scan protocol |
Illumina BeadArray Reader was used for scanning the arrays and Illumina BeadScan was used for image acquisition and recovery of primary data.
|
Description |
healthy donor1 blood spiked with 100 MCF7 cells
|
Data processing |
Raw data were generated using the Illumina BeadStudio 3.8 software and analyzed with R/Bioconductor. For each gene, only the probe with higher interquartile range was selected. According with the characteristics of the study, data normalization was not applicable
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|
|
Submission date |
Feb 28, 2014 |
Last update date |
Nov 21, 2014 |
Contact name |
Maurizio Callari |
E-mail(s) |
[email protected]
|
Organization name |
Fondazione IRCCS Istituto Nazionale dei Tumori
|
Street address |
Via Amadeo, 42
|
City |
Milan |
ZIP/Postal code |
20133 |
Country |
Italy |
|
|
Platform ID |
GPL14951 |
Series (1) |
GSE55470 |
Gene expression profiling of circulating tumor cells in breast cancer |
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