|
Status |
Public on Jul 15, 2021 |
Title |
ChIP-seq_H3K4me1_Vector |
Sample type |
SRA |
|
|
Source name |
THP-1 cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: Cultured THP-1 cells antibody: anti-H3K4Me1(Abcam ab8895)
|
Treatment protocol |
Media with 100 ng/ml of doxycycline was added
|
Growth protocol |
For THP-1 cell transduction, 1 × 106 THP-1 cells were transduced with 500 μl of 30-fold concentrated lentivirus through spin-inoculation at 25°C at 2200 rpm for 2 hours each for 3 times with 24 hours interval, and were cultured with 500 μg/ml of G418 (Invivogen) for selection for 12-14 days.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
For Chip-seq, genomic DNA were pulled down by antibodies. For RNA-seq, RNA was extracted with Qiagen miRNA-ease RNA extraction kit. HICHIP DNA was collected with Arima HICHIP kit. For ChIP-seq and HICHIP, library preparation using the NEBNext® Ultra™ II DNA Library Prep Kit for Illumina. For RNA-seq, NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina was used for library prepapration. Library quality was assessed by Tapstation and Qubit concentration measurement.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
RNA-seq reads were aligned to the human genome assembly GRCH38/hg38 or mouse genome assembly GRCm38/mm10 using STAR. RNA-seq counts were annotated using RSEM. Differentially expressed genes were calculated using DESeq2. ChIP-seq and PRO-seq sequence reads were aligned to the human genome assembly GRCH38/hg38 using BWA. Sam files were converted into bam files using Samtools. MACS2 was used to call peaks under the FDR threshold of 0.01. H3K4me3/H3K27ac HiChIP data were performed with MAPS. Genome_build: hg38 or mm10 Supplementary_files_format_and_content: Peak file, loop bedpe or gene count
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|
|
Submission date |
Jun 13, 2021 |
Last update date |
Jul 15, 2021 |
Contact name |
Bi Shi |
E-mail(s) |
bs6yk@virginia.edu
|
Phone |
2056433665
|
Organization name |
University of Virginia
|
Department |
Department of Biochemistry and Molecular Genetics
|
Lab |
Jiang Lab
|
Street address |
1340 JPA Pinn Hall Room 6017
|
City |
Charlottesville |
State/province |
Virginia |
ZIP/Postal code |
22908 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (1) |
GSE149420 |
UTX condensation underlies its tumor suppressive activity |
|
Relations |
BioSample |
SAMN19692542 |
SRA |
SRX11136858 |