Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Embryo
Cell type
Early embryos
NA
NA

Attributes by original data submitter

Sample

source_name
Drosophila early embryo
genotype/variation
elba2 mutant
tissue
early embyro
age
2-4 hours
molecule subtype
ChIPed genomic DNA
antibody
IgG control in ChIP

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Standard protocols were used to make chromatin extract for ChIP. Total RNAs were extracted with Trizol reagent for RNA-seq. Standard PRO-seq protocol was used to make PRO-seq libraries ChIP-seq libraries were made using NEB DNA library prep kit. ChIP-nexus library was made as previouly described (He, et al ,2015). RNA-seq libraries were made by using illumina True-seq total RNA library kit LT. PRO-seq libraries were made as previously described (Kwak, et al, 2013).

Sequencing Platform

instrument_model
Illumina HiSeq 2500

dm6

Number of total reads
30051912
Reads aligned (%)
82.7
Duplicates removed (%)
57.4
Number of peaks
2930 (qval < 1E-05)

dm3

Number of total reads
30051912
Reads aligned (%)
83.0
Duplicates removed (%)
54.6
Number of peaks
2026 (qval < 1E-05)

Base call quality data from DBCLS SRA