Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Others
Cell type
Tumor
NA
NA

Attributes by original data submitter

Sample

source_name
Tumor
classification
Neuroendocrine
ascl1 expression
Trp53;Rb1;Rbl2 triple knockout model
antibody
none

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For full ChIP protocol see Borromeo et al. Development. 2014. For extraction, nuclei were liberated from cells by dounce homogenization in PBS and then fixed in 1% formaldehyde for 10 minutes at room. temperature. Fixation was terminated by adding glycine to a final concentration of 0.125M. Chromatin was sheared by using a Diagenode Bioruptor for 30 minutes on high power with 30s:30s on:off cycles. 100 μg chromatin was immunoprecipitated with 5 μg affinity-purified mouse anti-ASCL1 antibody (BD Biosciences) followed by anti-mouse Dyna beads (Invitrogen). All libraries were made according to Illumina's or NEB (NEBNEXT) ChIP-seq DNA sample prep protocol

Sequencing Platform

instrument_model
Illumina HiSeq 2000

mm10

Number of total reads
74333914
Reads aligned (%)
90.7
Duplicates removed (%)
13.4
Number of peaks
759 (qval < 1E-05)

mm9

Number of total reads
74333914
Reads aligned (%)
90.4
Duplicates removed (%)
13.3
Number of peaks
863 (qval < 1E-05)

Base call quality data from DBCLS SRA