|
Status |
Public on Aug 03, 2012 |
Title |
input in Drosophila virilis |
Sample type |
SRA |
|
|
Source name |
embryo
|
Organism |
Drosophila virilis |
Characteristics |
developmental stage: embryo 0-12h fraction: input custom antibody: none
|
Treatment protocol |
no treatment
|
Growth protocol |
flies are kept at room temperature
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Two grams of embryos were used for two chromatin preparations, sonicated 20 cycles (10s on / 30s off) on a BRANSON SONIFIER 250 with output control set at 1.5. Libraries were prepared with the Illumina TruSeq DNA Sample Preparation Kit
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer II |
|
|
Description |
input in D. vir
|
Data processing |
Alignment: Sequence reads were obtained and mapped to the each genome build using Bowtie 0.12.7 software using the default setting. Genome Build: dvir1_2-input.bed: dvir1.2 flybase
|
|
|
Submission date |
Feb 09, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Jingping Yang |
E-mail(s) |
jpyang@nju.edu.cn
|
Organization name |
Nanjing University
|
Department |
Medical School
|
Street address |
22 Hankou Road
|
City |
Nanjing |
State/province |
Jiangsu |
ZIP/Postal code |
210000 |
Country |
China |
|
|
Platform ID |
GPL13312 |
Series (1) |
GSE35648 |
ChIP-seq study of BEAF binding in four Drosophila spcies |
|
Relations |
SRA |
SRX119309 |
BioSample |
SAMN00783963 |