| Accession | CRX280917 |
| Organism | Mus musculus |
| Accession in Other Database |
: |
| Title | SKOM+F-D5H3K9ac |
| BioProject | PRJCA006785 |
| BioSample | SAMC464021 |
| Platform | Illumina NovaSeq 6000 |
| Library |
| Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
Libraries were prepared according to Illumina's instructions accompanying the DNA Sample Kit (Part# 0801-0303). Briefly, DNA was end-repaired using a combination of T4 DNA polymerase, E. coli DNA Pol I large fragment (Klenow polymerase) and T4 polynucleotide kinase. The blunt, phosphorylated ends were treated with Klenow fragment (32 to 52 exo minus) and dATP to yield a protruding 3- 'A' base for ligation of Illumina's adapters which have a single 'T' base overhang at the 3’ end. After adapter ligation DNA was PCR amplified with Illumina primers for 15 cycles and library fragments of ~250 bp (insert plus adaptor and PCR primer sequences) were band isolated from an agarose gel. The purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the Genome Analyzer following the manufacturer's protocols. |
ChIP-Seq |
GENOMIC |
ChIP |
PAIRED
|
|
| Processing |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
|
| Release date | 2022-11-13 |
|---|
| Run |
| Run accession |
Run data file information |
| File name | File size (MB) |
|---|
| CRR328503 |
CRR328503_f1.fq.gz
CRR328503_r2.fq.gz
|
1,147.45
1,191.78
|
|
| Submitter | Li Wei (huitu09@163.com) |
|---|
| Organization | Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences |
|---|
| Date submitted | 2021-10-06 |
|---|
