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Status |
Public on Feb 22, 2018 |
Title |
WT Input for p300 |
Sample type |
SRA |
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Source name |
Th17 cells
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 tissue: Th17 differentiated in vitro for 3 days genotype: wild type chip antibody: None
|
Treatment protocol |
Naive CD4+ T cells were cultured under Th17 differentiation conditions for 3 days
|
Growth protocol |
RPMI-1640 medium with 10% FBS, 0.5ng/ml TGFβ and 20ng/ml IL-6
|
Extracted molecule |
genomic DNA |
Extraction protocol |
RNA was extracted from cells by Trizol. ChIP-seq was performed from crosslinked and MNase digested nuclear lysates; protein-DNA complexes were pulled down by indicated antibodies; after reverse-crosslinking, DNA was purified by phenol-chloroform. RNA libraries were prepared by the BerryGenomics company and only mRNA was used. ChIP libraries were constructed following the protocol of NEXTflex ChIP-Seq DNA Sequencing Kit(Bioo Scientific, 5143) described in the paper.
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
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Data processing |
Basecalls performed using bcl2fastq Conversion Software v1.8.4 RNA-seq reads were aligned to the mm10 genome using SOAP2. Reads count were calculated using htseq-count. ChIP-seq reads were aligned to the mm10 genome using bowtie. peaks were called using SICER version 1.1. Genome_build: mm10 Supplementary_files_format_and_content: wig files were generated using SICER version 1.1; tdf files were converted using igvtools.
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Submission date |
May 02, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Huiping Lu |
E-mail(s) |
luhuiping1@hotmail.com
|
Phone |
010-62797352
|
Organization name |
Tsinghua university
|
Street address |
Tsinghua university
|
City |
Beijing |
ZIP/Postal code |
100084 |
Country |
China |
|
|
Platform ID |
GPL17021 |
Series (1) |
GSE98427 |
Epigenetic activation during Th17 cell differentiation is impaired after TRIM28 deletion |
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Relations |
BioSample |
SAMN06859068 |
SRA |
SRX2775261 |