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Status |
Public on Jun 15, 2017 |
Title |
CLIP-seq analysis of NC-RNA interactions in wild-type and eccentric particles |
Organism |
Human immunodeficiency virus 1 |
Experiment type |
Other
|
Summary |
Nucleocapsid (NC) CLIP-seq experiments were conducted on wild-type and eccentric HIV-1 virions generated in the presence of allosteric integrase inhibitor, BI-B2.
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Overall design |
NC CLIP-seq experiments were conducted by immunoprecipitation of NC-RNA complexes from fully formed mature and eccentric virus particles. Libraries of RNA molecules bound by NC were generated and sequenced by Illumina Hi-Seq2500 platform.
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Contributor(s) |
Kutluay SB |
Citation(s) |
28615207 |
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Submission date |
Jun 14, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Sebla Bulent Kutluay |
E-mail(s) |
kutluay@wustl.edu
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Organization name |
Washington University School of Medicine
|
Street address |
Washington University School of Medicine
|
City |
Saint Louis |
State/province |
Missouri |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (1) |
GPL22068 |
Illumina HiSeq 2500 (Human immunodeficiency virus 1) |
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Samples (4)
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Relations |
BioProject |
PRJNA390491 |
SRA |
SRP109162 |