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Status |
Public on Dec 08, 2020 |
Title |
In situ HiC of primary mouse B cell progenitor populations after activation with LPS |
Organism |
Mus musculus |
Experiment type |
Other
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Summary |
Naive resting B-cells were purified from the bone marrow of C57BL/6 mice using flow cytometry sorting. Naive B cells were activated with LPS. Activated but undivided cells were harvested 3 hours, 10 hours or 33 hours after the LPS treatment. The Fluorescent Ubiquitination-based Cell Cycle Indicator (FUCCI) system was also used to isolate imminently dividing B cells specifically in the G1 stage of the cell cycle prior to the S phase.
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Overall design |
Two biological replicates were prepared at each activation time. In situ Hi-C libraries were sequenced on an Illumina NextSeq 500 to produce paired-end 81bp reads.
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Contributor(s) |
Coughlan HD, Smyth GK |
Citation(s) |
33637722 |
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Submission date |
Mar 24, 2020 |
Last update date |
Mar 09, 2021 |
Contact name |
Gordon K Smyth |
E-mail(s) |
smyth@wehi.edu.au
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Phone |
(+61 3) 9345 2326
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Fax |
(+61 3) 9347 0852
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URL |
http://www.wehi.edu.au
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Organization name |
Walter and Eliza Hall Institute of Medical Research
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Department |
Bioinformatics
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Lab |
Smyth
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Street address |
1G Royal Pde
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City |
Parkville |
State/province |
Vic |
ZIP/Postal code |
3052 |
Country |
Australia |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE147497 |
RNA-seq and in situ Hi-C of primary mouse B cell progenitor populations after activation with LPS |
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Relations |
BioProject |
PRJNA614943 |
SRA |
SRP253877 |