Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Prostate
Cell type
RWPE-1
Primary Tissue
Prostate
Tissue Diagnosis
Normal

Attributes by original data submitter

Sample

source_name
Human prostate cell line RWPE1
cell line
RWPE1
antibody
none

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For RNA-seq, RNA was extracted using Trizol reagent (15596-026) (Life technologies, Carlsbad, CA) following its protocol. For ChIP-seq, cells were crosslinked using 1% formaldehyde andl lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. RNA-seq libraries were made using KAPA Stranded mRNA-Seq Kit with KAPA mRNA Capture Beads (KK8420) (Kapa Biosystems, Woburn, MA). ChIP-seq: Libraries were barcoded (NEXTflex™ DNA Barcodes) (Bio Scientific, Austin, TX).

Sequencing Platform

instrument_model
NextSeq 500

hg38

Number of total reads
50157396
Reads aligned (%)
88.0
Duplicates removed (%)
15.7
Number of peaks
9982 (qval < 1E-05)

hg19

Number of total reads
50157396
Reads aligned (%)
83.2
Duplicates removed (%)
23.1
Number of peaks
7651 (qval < 1E-05)

Base call quality data from DBCLS SRA