Accession | CRX552215 |
Organism | Mus musculus |
Title | Mouse_embryos_E6.5_vitro |
BioProject | PRJCA013348 |
BioSample | SAMC998453 |
Platform | Illumina HiSeq 4000 |
Library |
Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
scRNA-seq libraries were constructed based on the modified single-cell tagged reverse transcription sequencing protocol. The single cell mRNAs in lysates were reverse-transcribed into the cDNAs with a primer containing a barcode and unique molecular identifiers. Subsequently, cDNAs with cell-specific barcodes were pooled together after amplification The cDNA products purified were indexed at the 3' ends of the cDNAs with biotin-amplification, followed by fragments of cDNAs using a Covaris system. Fragments with biotin tag at the 3' ends were enriched using Dynabeads MyOne Streptavidin C1 beads . Ultimately, the libraries were constructed using Kapa Hyper Prep Kits and sequenced on an Illumina HiSeq 4000 platform. |
RNA-Seq |
TRANSCRIPTOMIC SINGLE CELL |
PolyA |
PAIRED
|
|
Processing |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
|
Release date | 2022-11-24 |
Run |
Run accession |
Run data file information |
File name | File size (MB) |
CRR617215 |
CRR617215_f1.fastq.gz
CRR617215_r2.fastq.gz
|
8,175.52
7,983.36
|
CRR617216 |
CRR617216_f1.fastq.gz
CRR617216_r2.fastq.gz
|
8,294.52
8,510.19
|
CRR617217 |
CRR617217_f1.fastq.gz
CRR617217_r2.fastq.gz
|
9,727.55
8,938.47
|
CRR617218 |
CRR617218_f1.fastq.gz
CRR617218_r2.fastq.gz
|
7,863.72
7,416.62
|
|
Submitter | Qingyuan Zhu (zhuqingyuan@mail.tsinghua.edu.cn) |
Organization | Tsinghua University |
Date submitted | 2022-11-19 |