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Status |
Public on Jul 08, 2020 |
Title |
DE_BRD3IP_rep2: BRD3 ChIP-seq H1 hESC differentiated to definitive endoderm for 4 days |
Sample type |
SRA |
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Source name |
BRD3 H1 human Embryonic stem cells (hESC)
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Organism |
Homo sapiens |
Characteristics |
cell type: H1 human Embryonic stem cells (hESC) state: Differentiated in RPMI, B27 supplement, and 50 ng/mL activin
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Treatment protocol |
hESCs were differentiated for 4 days in RPMI with B27 supplement in the presence of 50 ng/ml activin A (R&D Systems) as previously described (Daneshvar et al., 2016)
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Growth protocol |
H1 (WA01) cells (WiCell) were cultured in mTeSR1 (Stem Cell Technologies) in feeder-free conditions as described (Daneshvar et al, 2016).
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Extracted molecule |
genomic DNA |
Extraction protocol |
BRD3 ChIP was pefromed using an anti-BRD3 (Bethyl A302-368A) ChIP-seq libraries were prepared according to instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina.
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
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Description |
The signal tracks of BRD3 ChIP of hESC differentiated at 4 hr after subtracting the background (WCE) (generated by MACS2)
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Data processing |
ChIP-seq data were mapped o human reference genome (hg38) by bowtie2. The mapped reads were processed using MACS2 to call peaks. Genome_build: hg38 Supplementary_files_format_and_content: Mapped ChIP-seq reads were processed with MACS2.
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Submission date |
Feb 16, 2019 |
Last update date |
Jul 08, 2020 |
Contact name |
Alan C. Mullen |
E-mail(s) |
mullenlabmgh@gmail.com
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Organization name |
Massachusetts General Hospital
|
Department |
Department of Medicine
|
Street address |
55 Fruit St.
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02135 |
Country |
USA |
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Platform ID |
GPL11154 |
Series (1) |
GSE126661 |
lncRNA DIGIT and BRD3 protein form phase-separated condensates to regulate endoderm differentiation |
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Relations |
BioSample |
SAMN10958784 |
SRA |
SRX5385028 |