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Status |
Public on Nov 14, 2014 |
Title |
Genome-wide map of H3K4me3 binding sites by ChIP-seq in human lymphoblastoid cell lines treated with doxorubicin |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We have used chromatin immune-precipitation with parallel sequencing (ChIP-Seq) technology to identify genome-wide H3K4me3 binding in human lymphoblastoid cell lines treated with a DNA-damaging chemotherapeutic reagent doxorubicin.
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Overall design |
ChIP-Seq analysis of H3K4me3 binding sites in human lymphoblastoid cells treated with Doxorubicin or vehicle
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Contributor(s) |
Su D, Wang X, Bell DA |
Citation(s) |
25569532 |
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Submission date |
Oct 25, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Xuting Wang |
E-mail(s) |
[email protected]
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Phone |
9842873840
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Organization name |
NIEHS/NIH
|
Street address |
111 TW Alexander Dr
|
City |
Research Triangle Park |
State/province |
NC |
ZIP/Postal code |
27709 |
Country |
USA |
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Platforms (1) |
GPL9115 |
Illumina Genome Analyzer II (Homo sapiens) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE51714 |
p53 activation effect on GM12878 lymphoblastoid cells |
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Relations |
BioProject |
PRJNA224699 |
SRA |
SRP031909 |