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Status |
Public on Aug 29, 2018 |
Title |
Genome-wide regulatory architecture maps using ATAC-seq, H3K4me2 ChIP-seq, and PEAT in Drosophila S2 cells and ATAC-seq in whole worms |
Organisms |
Caenorhabditis elegans; Drosophila melanogaster |
Experiment type |
Other Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To assess the organization of regulatory architecture across organisms, we performed ATAC-seq to identify accessible regions of chromatin, H3K4me2 ChIP-seq to measure regulatory status, and PEAT to measure Transcription start sites of stable transcripts in Drosophila S2 cells. For comparison, ATAC-seq for accessible chromatin measurement was performed in whole stage L3 worms.
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Overall design |
ATAC-seq, H3K4me2 ChIP-seq, and PEAT in Drosophila S2 cells and ATAC-seq in whole worms
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Contributor(s) |
Lacadie S, Ohler U, Ibrahim M |
Citation(s) |
30367057 |
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Submission date |
Aug 28, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Scott Allen Lacadie |
E-mail(s) |
scott.lacadie@mdc-berlin.de
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Organization name |
Max Delbrück Center for Molecular Medicine
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Department |
Berlin Institute for Medical Systems Biology
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Lab |
Ohler
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Street address |
Robert-Rössle-Str. 10
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City |
Berlin-Buch |
ZIP/Postal code |
13092 |
Country |
Germany |
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Platforms (2) |
GPL19132 |
Illumina NextSeq 500 (Drosophila melanogaster) |
GPL19757 |
Illumina NextSeq 500 (Caenorhabditis elegans) |
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Samples (8)
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Relations |
BioProject |
PRJNA400453 |
SRA |
SRP116321 |