Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Neural
Cell type
Neurons
NA
NA

Attributes by original data submitter

Sample

source_name
5-HT Neurons
cell/region
hPSC derived 5-HT neurons
chip antibody
Input
differentiation status
Differentiated 5-HT neurons

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Cell pellets (>10 x 10^6/n) and brain tissues were crosslinked and quenched. Samples were washed thoroughly before being subjected to lysis and sonication. Samples were then incubated with specific antibodies (7.5 μg/sample) bound to M-280 Dynabeads on a rotator at 4°C overnight. The following day, immunoprecipitates were washed, eluted and reverse crosslinked. Following RNA and protein digestion, DNA fragments were purified using a Qiagen PCR purification kit. RNA and ChIP libraries were prepared for sequencing using standard Illumina protocols

Sequencing Platform

instrument_model
Illumina HiSeq 4000

hg38

Number of total reads
49437924
Reads aligned (%)
98.7
Duplicates removed (%)
27.8
Number of peaks
1251 (qval < 1E-05)

hg19

Number of total reads
49437924
Reads aligned (%)
97.8
Duplicates removed (%)
29.1
Number of peaks
1224 (qval < 1E-05)

Base call quality data from DBCLS SRA