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GEO help: Mouse over screen elements for information. |
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Status |
Public on Jun 16, 2022 |
Title |
ChIP-Seq hnRNP E1, Cervical cancer SiHa cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Based on the specificity with which the unique KH structural domains of hnRNP E1 bind with RNA/DNA, considering that HPV16 provides RNA/DNA binding sites, we hypothesized that hnRNP E1 may be crucial to HPV16 oncogenes expression and cervical carcinogenesis. Based on the main purpose of this study was to explore the role of hnRNP E1 on the regulation of HPV16 oncogene expression in cervical cancerization, we conducted ChIP-seq in the untreated SiHa cell line.
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Overall design |
ChIP-Seq hnRNP E1, Cervical cancer SiHa cells
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Contributor(s) |
Wang J, Song L, Mao R, Ding L, Tian Z, Zhang M, Wang J, Wang M, Lyu Y, Liu C, Feng M, Jia H |
Citation(s) |
35800060 |
Submission date |
May 14, 2022 |
Last update date |
Jul 15, 2022 |
Contact name |
JinTao Wang |
E-mail(s) |
wangjt59@126.com
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Organization name |
Shanxi Medical University
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Department |
Department of Epidemiology, School of Public Health
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Street address |
56 Xin Jian Nan Road
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City |
Taiyuan City |
State/province |
Shanxi |
ZIP/Postal code |
030001 |
Country |
China |
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Platforms (1) |
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Samples (4)
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Relations |
BioProject |
PRJNA838137 |
Supplementary file |
Size |
Download |
File type/resource |
GSE203023_RAW.tar |
248.1 Mb |
(http)(custom) |
TAR (of TAR) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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