|
Status |
Public on May 14, 2021 |
Title |
mESC_DNA_cell132 |
Sample type |
SRA |
|
|
Source name |
cell line
|
Organism |
Mus musculus |
Characteristics |
cell type: cultured mouse embryonic stem cells strain: C57BL/6 chip antibody: H3K4me3, Millipore 04-745, lot:3243412, H3K27me3,millipore 07-449, #3146226
|
Treatment protocol |
The mESCs were dissociated by 0.1% Trypsin digestion, and aliquot of cell numbers were directly used for CoTECH
|
Growth protocol |
mESCs were cultured at 37 °C with 5% CO2 and was maintained in high glucose DMEM
|
Extracted molecule |
genomic DNA |
Extraction protocol |
folloing CoTECH protocol After PCR enrichment using Q5 polymerase, the 300-1,000 bp fragments were isolated using the 1.5% (w/v) agarose gel and purified once with 0.8 x AMpure XP beads
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
Basecalls performed using CASAVA version 1.8.2. For ChIP part, Reads were de-multiplexed to generate single cell profiles by custom scripts. Reads were aligned to mouse genome mm10 by bowtie2 (v 2.3.1) (ChIP part) and Hisat2 (version 2.0.4) (RNA part). ChIP part: Reads whose MAPQ >= 30 were determined as uniquely mapping reads. Duplication reads were removed by Picard. RNA part: reads were counted by HTSeq. Genome_build: mm10 Supplementary_files_format_and_content: The processed files were aggregate bigwig files.
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|
|
Submission date |
May 13, 2021 |
Last update date |
May 15, 2021 |
Contact name |
Haiqing Xiong |
E-mail(s) |
haiqingxiong@pku.edu.cn
|
Organization name |
Peking University
|
Street address |
5 Yiheyuan Road, Haidian District
|
City |
Beijing |
State/province |
Beijing |
ZIP/Postal code |
100871 |
Country |
China |
|
|
Platform ID |
GPL24247 |
Series (1) |
GSE158435 |
Single-cell joint detection of chromatin occupancy and transcriptome enables higher-dimensional epigenomic reconstructions |
|
Relations |
BioSample |
SAMN19164778 |
SRA |
SRX10882008 |