|
Status |
Public on Jan 05, 2015 |
Title |
H2A.Z_ChIPSeq_WT_rep2 |
Sample type |
SRA |
|
|
Source name |
Saccharomyces cerevisiae grown in SD medium
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: MATalpha can1-delta::STE2pr-SP_his5 lyp1-delta his3-delta-1 ura3-delta-0 met15-delta-0 HTZ1-HpH chip antibody: anti-Htz1
|
Treatment protocol |
None
|
Growth protocol |
Yeast cells were grown in SD medium to mid-log phase before harvesting for ChIP or RNA extraction.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Cultures were crosslinked with 1% (v/v) formaldehyde, quenched with glycine, and cells were lysed with beads in a FastPrep-24 (MP Biomedicals) cell homogeniser. Sonicated, clarified extracts were immunoprecipitated with anti-Htz1 antibodies before washing and DNA extraction, or were used directly to prepare input DNA. Illumina TruSeq ChIP Sample Prep Kit were used for library preparation.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
Htz1 ChIP-seq of wild type S.cerevisiae, replicate 2
|
Data processing |
Sequence reads were mapped to the S. cerevisiae genome assembly sacCer1 using Bowtie version 0.12.9, allowing up to 2 mismatches and no ambiguously mapped reads.Mapped reads were then converted to WIG files.
Genome_build: sacCer1
Supplementary_files_format_and_content: BedGraph (WIG)
|
|
|
Submission date |
Jan 15, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Muxin Gu |
E-mail(s) |
muxingu@gmail.com, mg445@cam.ac.uk
|
Phone |
01223767800
|
Organization name |
University of Cambridge
|
Department |
Haematology
|
Lab |
George Vassiliou
|
Street address |
Jeffrey Cheah Biomedical Centre, Puddicombe Way
|
City |
Cambridge |
ZIP/Postal code |
CB2 0AW |
Country |
United Kingdom |
|
|
Platform ID |
GPL13821 |
Series (1) |
GSE54105 |
H2A.Z marks antisense promoters and has positive effects on antisense transcript levels in budding yeast |
|
Relations |
BioSample |
SAMN02585014 |
SRA |
SRX433135 |