Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Adult
Cell type
Ovary
NA
NA

Attributes by original data submitter

Sample

source_name
ovary
strain/cell line background
w1118
tissue/cell type
ovary
genotype/variation
Panx het KO
chip antibody
none

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For samples 1-24: Samples were crosslinked in formaldehyde and lysed, followed by sonication. For samples 25-32: OSCs were resuspended in Trizol, flies homogenized in Trizol. RNA was isolated using RNeasy mini prep column (Qiagen). For samples 33-36: Flies were homogenized in Trizol and RNA extracted using Phenol/Chloroform For samples 1-24: NEBNext® Ultra™ II DNA Library Prep Kit for Illumina® For samples 25-32: NEBNext Poly(A) mRNA magnetic Isolation Module (NEB), followed by NEBNext Ultra Directional RNA Library Prep kit for Illumina (NEB) For samples 33-36: Adapted from: Jayaprakash, Anitha D. et al. “Identification and Remediation of Biases in the Activity of RNA Ligases in Small-RNA Deep Sequencing.” Nucleic Acids Research 39.21 (2011): e141. PMC. Web. 22 Oct. 2018.

Sequencing Platform

instrument_model
Illumina HiSeq 4000

dm6

Number of total reads
25358795
Reads aligned (%)
97.0
Duplicates removed (%)
27.1
Number of peaks
0 (qval < 1E-05)

dm3

Number of total reads
25358795
Reads aligned (%)
97.2
Duplicates removed (%)
25.6
Number of peaks
367 (qval < 1E-05)

Base call quality data from DBCLS SRA