|
Status |
Public on Apr 03, 2014 |
Title |
ChIP-Seq Analysis of PC in S2 cells, first replicate |
Sample type |
SRA |
|
|
Source name |
PC 1
|
Organism |
Drosophila melanogaster |
Characteristics |
chip antibody: Polycomb cell line: S2
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Purified ChIP-DNA was prepared for sequencing on a HiSeq 2000 sequencer using Illumina standard protocol. TruSeq ChIP Sample Preparation Kit
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Basecalling, CASAVA 1.8.2, Illumina Alignment on dm3, CASAVA 1.8.2, Illumina Quality measures with FastQC Peak calling using MACS 1.4.2 Assignment to genes using Perl scripts Genome_build: dm3 Supplementary_files_format_and_content: bed peak files
|
|
|
Submission date |
Feb 24, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Giacomo Cavalli |
E-mail(s) |
giacomo.cavalli@igh.cnrs.fr
|
Organization name |
CNRS
|
Lab |
INSTITUTE of HUMAN GENETICS
|
Street address |
IGH - CNRS, 141, rue de la Cardonille
|
City |
Montpellier |
ZIP/Postal code |
34396 Cedex5 |
Country |
France |
|
|
Platform ID |
GPL13304 |
Series (1) |
GSE55303 |
Identification of new regulators of the three dimensional Polycomb organization by a microscopy-based genome-wide RNAi screen |
|
Relations |
BioSample |
SAMN02650909 |
SRA |
SRX475424 |