|
Status |
Public on Aug 24, 2017 |
Title |
ChIP-seq_K562_NUP153 |
Sample type |
SRA |
|
|
Source name |
Human K562 cells
|
Organism |
Homo sapiens |
Characteristics |
cell line: K562 chip antibody: BioLegend, 906201, B215613
|
Growth protocol |
Human K562 cells were cultured in IMDM supplemented with 10% heat-inactivated fetal bovine serum (FBS) and 2% penicillin-streptomycin. KH2 cells were cultured on primary embryonic fibroblasts in standard ES medium and differentiated to EBs by LIF withdrawal for 8 days.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
For ChIP-seq analysis using the Illumina NextSeq500, 10-20 ng of ChIP DNA was processed for library generation using the NEBNext ChIP-seq Library Prep Master Mix following the manufacturer’s protocol (New England Biolabs). Raw reads that aligned to exactly one location in the reference human genome (hg19) were retained for downstream data analysis.
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
Sequencing reads were aligned to human genome assembly hg19 (NCBI version 37) using Bowtie v1.0.0 with the following parameters: --best --strata -k 1 -m 1. Duplicate reads were removed after the aligment with the Picard command-line tools. Peak detection was performed with the Model-based Analysis of ChIP-Seq (MACS) algorithm (http://liulab.dfci.harvard.edu/MACS/). The wig files were generated by a moving window of size 200bp. The tag count in the windown was further normalized by total read count for ChIP-seq data generated by NextSeq500. Genome_build: hg19 Supplementary_files_format_and_content: wig file and peak bed file
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|
|
Submission date |
May 22, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Jian Xu |
E-mail(s) |
Jian.Xu@stjude.org
|
Phone |
9015955208
|
Organization name |
St. Jude Children's Research Hospital
|
Department |
Pathology
|
Street address |
262 Danny Thomas Place, MS 345
|
City |
Memphis |
State/province |
Tennessee |
ZIP/Postal code |
38105 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (2) |
GSE88817 |
In situ CAPTURE of chromatin interactions by biotinylated dCas9 |
GSE99178 |
ChIP-seq analysis of BRD4 and RNAPII in K562 cells treated with DMSO or JQ1, NUP98 and NUP153 in K562 cells, and H3K27ac in mouse KH2 undifferentiated embryonic stem cells (ESCs) or differentiated embryonic bodies (EBs) |
|
Relations |
BioSample |
SAMN07154429 |
SRA |
SRX2841999 |