|
Status |
Public on Aug 20, 2010 |
Title |
Yeast-Ecoli control, Mnase |
Sample type |
SRA |
|
|
Source name |
Yeast-Ecoli mixture
|
Organisms |
Escherichia coli; Saccharomyces cerevisiae |
Characteristics |
strain (yeast): BY4730 (MAT a, leu2∆0, met15∆0, ura3∆0) strain (e. coli): JS5
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA from S.cerevisiae and E.coli was purified using Qiagen genomic tip 500/G, and mixed in a 3:1 mass ratio. The mixture was treated with MNase (USB) to yield a small average fragment size (< 300 bp), and DNA fragments of approximately 150 bp were purified by excision from an agarose gel.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer |
|
|
Data processing |
Mononucleosome size DNA fragments were sequenced using Illumina Genome Analyzer, and mapped to the S.cerevisiae genome (SGD April 2008 build) and to the E.coli K12 genome (U00096), allowing up to 2 mismatches per read. Raw sequence read data are unavailable
|
|
|
Submission date |
Aug 19, 2010 |
Last update date |
Jun 11, 2013 |
Contact name |
George Locke |
E-mail(s) |
glocke@physics.rutgers.edu
|
Phone |
(732) 445-3156
|
Fax |
(732) 445-5958
|
URL |
http://nucleosome.rutgers.edu/
|
Organization name |
Rutgers University
|
Department |
Physics
|
Street address |
136 Frelinghuysen Rd
|
City |
Piscataway |
State/province |
NJ |
ZIP/Postal code |
08854 |
Country |
USA |
|
|
Platform ID |
GPL10839 |
Series (1) |
GSE23712 |
High-throughput sequencing reveals a simple model of nucleosome energetics |
|
Relations |
BioSample |
SAMN02195988 |