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Status |
Public on Jun 20, 2018 |
Title |
mRNA profiles of active hematopoieitc stem cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Purpose: The goals of this study are to elucidate the underlying mechanism for the activation of HSCs Methods: After wild type (WT) HSCs (CD150+ CD48- EPCR+ Lineage-) were treated with 5-fluorouracil (5-FU), 100 cells of HSCs were sorted. Moreover, after the culture with or without Nifedipien, cultured HSC fraction (CD150+ CD48- EPCR+ c-kit+ Sca-1+ Lineage-) were sorted. These cells were subjected to mRNA sequence using Next-seq (n>3). The sequence reads that passed quality filters were analyzed by CLC genomic workbench.
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Overall design |
After the culture with or without Nifedipine, HSCs wihtin 3 cell division population were sorted, and subsequently mRNA profiles were generated by deep sequencing using Next-seq (n>3). Using HSCs derived from untreated and 5-FU-treated mice, mRNA profiles were generated by deep sequencing using Next-seq (n>4).
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Contributor(s) |
Umemoto T, Suda T |
Citation(s) |
29946000 |
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Submission date |
Feb 26, 2018 |
Last update date |
Mar 25, 2019 |
Contact name |
Terumasa Umemoto |
Organization name |
Kumamoto University
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Street address |
2-2-1, Honjo, Chuo-Ku
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City |
Kumamoto |
ZIP/Postal code |
862-0957 |
Country |
Japan |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (15)
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Relations |
BioProject |
PRJNA435963 |
SRA |
SRP133481 |
Supplementary file |
Size |
Download |
File type/resource |
GSE111118_RAW.tar |
11.3 Mb |
(http)(custom) |
TAR (of TXT) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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