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Status |
Public on Jan 12, 2019 |
Title |
input_exo1_sgs1_4 |
Sample type |
SRA |
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Source name |
input_exo1_sgs1_4
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Organism |
Saccharomyces cerevisiae |
Characteristics |
background strain: W303 genotype/variation: exo1delta sgs1delta time point: after 4 hours of DSB induction antibody: none
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Extracted molecule |
genomic DNA |
Extraction protocol |
bead beater lysis, shearing by sonication, RNAseA digest, de-crosslinking, phenol-chloroform extraction MicroPlex Library Preparation kit v2 (Diagenode)
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 1500 |
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Data processing |
Raw datas quality was check using the fastqc tool (v. 0.11.2) the raw data was mapped to the S. cerevisiae genome, excluding multimapped reads (option -m 1) Using the R (v. 3.22) package GenomicRanges (v. 1.22) the files converted into binned table with a windows size of 1000bp. the regions in the bam files overlapped the binned regions of the genome were normalized using the TMM normalisation from the edgeR packge (v. 3.12.0) the table were than converted into wig files for better visulization Genome_build: Ensembl, build R64-1-1 Supplementary_files_format_and_content: wig files were generated using the R software suite.
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Submission date |
Jan 11, 2019 |
Last update date |
Jan 13, 2019 |
Contact name |
Susanne Charlotte Sophie Bantele |
E-mail(s) |
sbantele@biochem.mpg.de
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Organization name |
Max Planck Institute of Biochemistry
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Department |
NWG
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Lab |
DNA REP (Pfander)
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Street address |
Am Klopferspitz 18
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City |
Martinsried/Munich |
State/province |
Bavaria |
ZIP/Postal code |
82152 |
Country |
Germany |
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Platform ID |
GPL18085 |
Series (1) |
GSE124948 |
Quantitative sensing and signalling of single-stranded DNA during the DNA damage response |
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Relations |
BioSample |
SAMN10724593 |
SRA |
SRX5241182 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data not applicable for this record |
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