|
Status |
Public on Mar 12, 2016 |
Title |
ume6_Chd1Ume6_MNase |
Sample type |
SRA |
|
|
Source name |
ume6_Chd1Ume6_MNase
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain background: W303 auxotroph genotype/variation: ume6 deletion with hybrid remodeling protein matched wild type sample: 1
|
Treatment protocol |
cells were treated with zymolyase and spheroplasts were treated with MNase and ExoIII to produce nucleosome ladders corresponding to roughly 80% mononucleosomes
|
Growth protocol |
log cells were grown to OD600 0.4 to 0.6
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was purified by phenol/chloroform and mononucleosome size fragments were purified from an agarose gel for library construction TruSeq protocol (Illumina) was followed
|
|
|
Library strategy |
MNase-Seq |
Library source |
genomic |
Library selection |
MNase |
Instrument model |
Illumina Genome Analyzer |
|
|
Data processing |
Basecalling was performed by Illumina CASAVA software package Reads were mapped to S. cerevisiae genome (Saccharomyces_cerevisiae.EF4.65.dna.toplevel.fa) with Tophat2 Mapped reads were filtered using SAMtools flags -f 3 -F 256 Dyads were calculated by taking the midpoint of paired-end reads from fragments between 100 and 200 bp Data were normalized such that average value at a genomic position was 1.0 Between-strain comparisons were done using best-matched MNase digests. For isw2-related parent strains, wild-type 2 is best-matched. For ume6-related strains, wild-type 1 is best-matched. For WT +Chd1Ume6, wild-type 1 is best-matched. Genome_build: Saccharomyces_cerevisia.EF4.65 Supplementary_files_format_and_content: coverage file with tab-delimited chromosome/position/normalized dyad counts
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|
|
Submission date |
Sep 01, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Jeffrey N McKnight |
E-mail(s) |
[email protected]
|
Organization name |
University of Oregon
|
Department |
Institute of Molecular Biology
|
Lab |
McKnight Lab
|
Street address |
1229 University of Oregon, 1318 Franklin Blvd, Rm 273 Onyx Bridge
|
City |
Eugene |
State/province |
OR |
ZIP/Postal code |
97408 |
Country |
USA |
|
|
Platform ID |
GPL9134 |
Series (2) |
GSE72570 |
Sequence-Targeted Nucleosome Sliding in vivo - Nucleosome Mapping |
GSE72572 |
Sequence-Targeted Nucleosome Sliding in vivo |
|
Relations |
BioSample |
SAMN04024964 |
SRA |
SRX1176425 |