Accession | CRX248238 |
Organism | Mus musculus |
Title | spermatid_12 |
BioProject | PRJCA005396 |
BioSample | SAMC392345 |
Platform | Illumina HiSeq X Ten |
Library |
Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
For DNA part, the magnetic beads containing cell nuclei (DNA) were treated with EZ-96 DNA Methylation-Direct MagPrep kit (Zymo, Cat. D5044) to complete the bisulfite conversion. Then four rounds of amplification were conducted by Klenow exo- (ENzymics, Cat. NG202) and scBS-seq-P5-N6-oligo1 (CTACACGACGCTCTTCCGATCTNNNNNN). The purified products were used to perform the second strand synthetizations using scBS-seq-P7-N6-oligo2 (AGACGTGTGCTCTTCCGATCTNNNNN). Finally, the DNA library were constructed with incorporated universal primers and index primers (New England Biolabs). After purification twice with 0.8×AMPure XP beads the DNA libraries were checked for quality and each cell was sequenced for about 3Gb on Illumina Hiseq Xten platform (Novogene). |
Bisulfite-Seq |
GENOMIC SINGLE CELL |
other |
PAIRED
|
|
Processing |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
|
Release date | 2022-06-28 |
Run |
Run accession |
Run data file information |
File name | File size (MB) |
CRR291821 |
CRR291821_f1.fastq.gz
CRR291821_r2.fastq.gz
|
1,084.3
1,122.94
|
|
Submitter | Xiaoyang Zhao (zhaoxiaoyang@smu.edu.cn) |
Organization | Southern Medical University |
Date submitted | 2021-06-13 |