|
Status |
Public on Nov 20, 2022 |
Title |
CHIP-SEQ H3K27AC in neuron |
Sample type |
SRA |
|
|
Source name |
iPSC derived human cortical neuron
|
Organism |
Homo sapiens |
Characteristics |
cell type: iPSC derived cortical neuron disease state: non-diseased chip antibody: H3K27Ac (ActiveMotif, catalog# 39133).
|
Growth protocol |
iPSC neurons were obtained from Cellular dynamics, and were harvested in post-plate day 14.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
CHIP-SEQ was based on Standard protocols used in ENCODE
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
NextSeq 550 |
|
|
Data processing |
CHIP-SEQ was based on Standard protocols used in ENCODE CHIP-SEQ: Alignment by BWA CHIP-SEQ: Peak call by GEM Supplementary_files_format_and_content: CHIP-SEQ: Regulatory peaks are listed Genome_build: hg19
|
|
|
Submission date |
Apr 05, 2016 |
Last update date |
Nov 20, 2022 |
Contact name |
Jingjing Li |
E-mail(s) |
[email protected]
|
Organization name |
Stanford University
|
Street address |
3165 Porter Drive
|
City |
Palo Alto |
ZIP/Postal code |
94304 |
Country |
USA |
|
|
Platform ID |
GPL21697 |
Series (1) |
GSE79965 |
Regulatory genomic profiling in pure iPSC-derived human cortical neurons |
|
Relations |
BioSample |
SAMN04620191 |
SRA |
SRX1683035 |