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Sample GSM1671317 Query DataSets for GSM1671317
Status Public on Apr 30, 2015
Title GMP_AE1_1
Sample type RNA
 
Source name FACS-sorted GMP cells (LeuA/AE1)
Organism Mus musculus
Characteristics strain background: C57BL/6
transplanted with: splenic cells from moribond Tet2-/-:AE leukemic mice (LeuA/AE1)
tissue: bone marrow of recipient mice
cell type: FACS-sorted in vivo GMP cells (Lin-cKit+Sca1-CD16/32+CD150-)
arrayslide: 252800516543
subarray id: 2_1
Treatment protocol N/A
Growth protocol FACS-sorted in vivo GMP cells (Lin-cKit+Sca1-CD16/32+CD150-) were isolated from bone marrow of recipient mice one month after transplantation of WT bone marrow or splenic cells from two independent moribond Tet2-/-:AE leukemic mice (LeuA/AE1 or LeuB/AE3)
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using the Allprep Micro Kit (Qiagen)
Label Cy3
Label protocol Biological triplicates were labeled and hybridized to Agilent SurePrint G3 Mouse GE 8x60K arrays according to manufacturers instructions
 
Hybridization protocol standard Agilent procedure
Scan protocol standard Agilent procedure
Description Gene expression data from in vivo FACS-sorted GMP cells isolated from secondary recipients transplanted with leukemic splenocytes (LeuA)_Biological replicate 1
Data processing Agilent microarrays were normalized using the RMA function from the Bioconductor affy package (Gautier et al., 2004). The normalized arrays were then background corrected using the normal+exponential convolution model with saddle-point approximation to maximum likelihood (Ritchie et al., 2007) and normalized between arrays by Cyclic Loess using the limma package implementation (Smyth and Speed, 2003). In the processed data file, spike-in and control probes were removed and the remaining probe list was collapsed based on unique identifiers to only retain the best probe (lowest p-value) for a given transcript. This yielded a final processed data file containing a total of 37877 rows.
 
Submission date Apr 29, 2015
Last update date Apr 30, 2015
Contact name Kasper Dindler Rasmussen
E-mail(s) [email protected]
Organization name School of Life Sciences, University of Dundee
Department Division of Molecular, Cellular, and Developmental Biology (MCDB)
Street address Dow Street
City Dundee
ZIP/Postal code DD1 5EH
Country United Kingdom
 
Platform ID GPL10787
Series (2)
GSE59591 Loss of TET2 in hematopoietic cells leads to DNA hypermethylation of active enhancers and induction of leukemogenesis
GSE68415 Loss of TET2 in hematopoietic cells leads to DNA hypermethylation of active enhancers and induction of leukemogenesis [Agilent]

Data table header descriptions
ID_REF
VALUE normalized

Data table
ID_REF VALUE
A_66_P140974 6.612772359
A_66_P140973 6.075194594
A_66_P140949 13.93251022
A_66_P140886 12.90156494
A_66_P140874 6.200362054
A_66_P140858 13.47613182
A_66_P140856 6.729154387
A_66_P140855 6.088210265
A_66_P140812 5.922500405
A_66_P140794 7.581883724
A_66_P140742 6.612772359
A_66_P140712 6.243314291
A_66_P140711 17.34714632
A_66_P140699 6.325562915
A_66_P140688 6.584655732
A_66_P140658 8.246511703
A_66_P140613 8.788923582
A_66_P140599 9.129087296
A_66_P140574 6.742689391
A_66_P140570 6.558533475

Total number of rows: 37877

Table truncated, full table size 949 Kbytes.




Supplementary file Size Download File type/resource
GSM1671317_SG12524268_252800516543_S001_GE1_1100_Jul11_2_1.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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