|
Status |
Public on Aug 31, 2017 |
Title |
S2-AbdA_Input_C |
Sample type |
SRA |
|
|
Source name |
S2-HA::AbdA Cell line
|
Organism |
Drosophila melanogaster |
Characteristics |
cell line: late embryo-derived cell line stably transfected with HA::AbdA strain: S2-DRSC-HA::AbdA genotype: HA::AbdA treatment: 10 microMolar Cu2SO4
|
Treatment protocol |
Cells were treated with 10 microMolar Copper Sulphate for 24 h prior to chromatin and RNA preparation
|
Growth protocol |
Cells were grown in T-flasks to a density of not more than 7x10^6 cells/ml in Schneider Medium supplemented with 10% FBS
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Chromatin was prepared according to the modENCODE procedure; RNA was extracted with Qiagen Rneasy kit DNA libraries were prepared according to Illumina's instructions; RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
ChIP Input (Code C)
|
Data processing |
Basecalls performed using RTA (Illumina) ChIP-seq reads were aligned to the dm3 genome assembly using BWA v0.7.12 using default parameters ChIP-Seq peak calling was performed using MACS2 (v0.7.12) using low stringency on individual replicates. Final peaks were called using an Irreproducible Discovery Rate (IDR) of 1% according to guidelines set out by the ENCODE consortium. ChIP-seq bigWig files of enrichment >0 were produced using spp using merged replicate bamfiles that had been randomly downsampled to have equal numbers of reads between samples from S2 cells and those from S2-HA::AbdA cell line Genome_build: dm3 Supplementary_files_format_and_content: BigWig files were prepared using spp and show ChIP enrichment values >0; Bed files were prepared using MACS2 and represent peaks called in both replicates having an IDR of 1%.
|
|
|
Submission date |
Jul 18, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Andrew J Saurin |
E-mail(s) |
[email protected]
|
Organization name |
IBDM / CNRS
|
Street address |
Campus de Luminy
|
City |
Marseille |
ZIP/Postal code |
13009 |
Country |
France |
|
|
Platform ID |
GPL13304 |
Series (2) |
GSE101554 |
Genomic binding profiling upon expression of AbdA in S2 cells |
GSE101557 |
Expression of Hox transcription factors in Drosophila S2 cells |
|
Relations |
BioSample |
SAMN07360991 |
SRA |
SRX3011256 |