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Status |
Public on Feb 15, 2018 |
Title |
ChIP-Seq of H3K9me3 and H3K36me3 after GFP or dKDM4A RNAi of S2 cells |
Organism |
Drosophila melanogaster |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Analysis of H3K9me3 and H3K36me3 levels in unique and repetitive regions of Drosophila genome after GFP (control) or dKDM4A RNAi of S2 cells
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Overall design |
After 5 days of RNAi, chromatin was prepared by fixation of 2x10^7 S2 cells with 1% paraformaldehyde for 10 minutes and shearing with Bioruptor sonicator (30 cycles). ChIP was performed by overnight incubation of chromatin with Protein-A Dynabeads and 5 ug of either anti-H3K36me3 or anti-H3K9me3 ChIP-grade antibody (Abcam). Library construction was conducted using TruSeq DNA sample preparation kit (Illumina). All sequencing data were obtained from the Vincent J. Coates Genomics Sequencing Laboratory at UC Berkeley.
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Contributor(s) |
Colmenares SU, Karpen GH |
Citation(s) |
28743002 |
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Submission date |
May 17, 2017 |
Last update date |
May 15, 2019 |
Contact name |
serafin colmenares |
E-mail(s) |
[email protected]
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Organization name |
lawrence berkeley national lab
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Street address |
1 cyclotron road MS977R180A
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City |
berkeley |
ZIP/Postal code |
94720 |
Country |
USA |
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Platforms (1) |
GPL13304 |
Illumina HiSeq 2000 (Drosophila melanogaster) |
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Samples (12)
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GSM2630590 |
GFPRNAi_H3K36Me3ChIP3.filtered.fastq.gz |
GSM2630591 |
GFPRNAi_H3K36Me3ChIP4_filtered.fastq.gz |
GSM2630592 |
GFPRNAi_H3K9Me3ChIP3_filtered.fastq.gz |
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Relations |
BioProject |
PRJNA387028 |
SRA |
SRP107219 |