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Status |
Public on Jun 18, 2015 |
Title |
gammaH2Av ChIP-seq in Drosophila stage 10B and 13 follicle cells |
Organism |
Drosophila melanogaster |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We analyzed gamaH2Av ChIP-seq from hand dissected stage 10B and 13 follicle cell nuclei. Egg chambers were dissected from wild-type (OrR) or H2Av[ΔCT] ovaries to assess binding at the Drosophila Follicle Cell Amplicons and across the genome.
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Overall design |
ChIP-seq of gammaH2Av bound to follicle cell DNA from stage 10B and 13 egg chambers, collected from wild-type (OrR) and H2Av[ΔCT] Drosophila ovaries. Sequences analyzed by Illumina sequencing. Two replicates are included for each ChIP reaction.
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Contributor(s) |
Alexander JL, Barrasa MI, Orr-Weaver TL |
Citation(s) |
26051888 |
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Submission date |
Mar 09, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Terry L. Orr-Weaver |
E-mail(s) |
weaver@wi.mit.edu
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Phone |
617-258-5251
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Organization name |
Whitehead Institute for Biomedical Research
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Lab |
Orr-Weaver
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Street address |
9 Cambridge Center
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City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02142 |
Country |
USA |
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Platforms (1) |
GPL13304 |
Illumina HiSeq 2000 (Drosophila melanogaster) |
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Samples (16)
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This SubSeries is part of SuperSeries: |
GSE66691 |
Replication fork progression during re-replication requires the DNA damage checkpoint and double-strand break repair |
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Relations |
BioProject |
PRJNA277729 |
SRA |
SRP055999 |