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Status |
Public on Mar 12, 2016 |
Title |
Sequence-Targeted Nucleosome Sliding in vivo - Nucleosome Mapping |
Organism |
Saccharomyces cerevisiae |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Nucleosome positions were determined in wild type cells, cells lacking Isw2 or Ume6, and cells containing a hybrid Chd1-Ume6 chimeric remodeler
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Overall design |
Matched MNase digests from W303 strain variants during log growth (OD600=0.4-0.6) were subject to paired-end sequencing for nucleosome mapping. For effects of the engineered fusion remodeling protein, a catalytically inactive (ATPase dead D513N) variant was included as a control.
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Contributor(s) |
McKnight JN, Tsukiyama T, Bowman GD |
Citation(s) |
26993344 |
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Submission date |
Sep 01, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Jeffrey N McKnight |
E-mail(s) |
jmcknig2@uoregon.edu
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Organization name |
University of Oregon
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Department |
Institute of Molecular Biology
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Lab |
McKnight Lab
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Street address |
1229 University of Oregon, 1318 Franklin Blvd, Rm 273 Onyx Bridge
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City |
Eugene |
State/province |
OR |
ZIP/Postal code |
97408 |
Country |
USA |
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Platforms (1) |
GPL9134 |
Illumina Genome Analyzer (Saccharomyces cerevisiae) |
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Samples (13)
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This SubSeries is part of SuperSeries: |
GSE72572 |
Sequence-Targeted Nucleosome Sliding in vivo |
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Relations |
BioProject |
PRJNA294376 |
SRA |
SRP063046 |