|
Status |
Public on Feb 21, 2012 |
Title |
pol32_OF_sample |
Sample type |
SRA |
|
|
Source name |
pol32_OF
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: pol32ko [yIW174] cell cycle stage: Asynchronous culture
|
Growth protocol |
Cells were grown at 30 degrees in YEP + 2% raffinose to O.D. 0.3, then shifted to 37 degrees after addition of galactose to 2% and doxycycline to 40ug/ml
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was purified and heat-denatured: DNA was bound to Source 15Q resin in batch at 300mM NaCl, pH12, and eluted in 50mM steps. Fractions from 800-900 mM were collected, neutralized and concentrated by precipitation. Double-stranded sequencing adaptors with N6 random overhangs ligated to each end; after second-strand synthesis using Taq, material from 200-1000bp was gel-purified and amplified by PCR. Products from 200-800 bp were gel-purified from two successive 2.5% agarose gels
|
|
|
Library strategy |
OTHER |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
Columns in the bed file are as follows: column 1: chromosome column 2: range first bp column 3: range last bp column 4: length of fragment in bp column 5: count of reads column 6: strand
|
Data processing |
Data were aligned to the May 2008 build of the S. cerevisiae genome: paired-end reads each beginning with a 20bp perfect match to a unique genomic locus and within 1kb of one another were considered.
|
|
|
Submission date |
Nov 17, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Iestyn Whitehouse |
E-mail(s) |
[email protected]
|
Organization name |
Sloan-Kettering Institute
|
Department |
Molecular Biology
|
Street address |
1275 York Avenue
|
City |
New York |
State/province |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
|
|
Platform ID |
GPL13821 |
Series (1) |
GSE33786 |
Intrinsic Coupling of Lagging Strand Synthesis to Chromatin Assembly |
|
Relations |
SRA |
SRX105999 |
BioSample |
SAMN00759072 |