|
Status |
Public on Feb 17, 2023 |
Title |
E50, embryo B, part 1, scRNAseq |
Sample type |
SRA |
|
|
Source name |
embryo
|
Organism |
Callithrix jacchus |
Characteristics |
tissue: embryo developmental stage: embryonic day 50
|
Extracted molecule |
total RNA |
Extraction protocol |
Approximately 1/3 of posterior part of CS12 fetus (Fig XX) were dissociated into single cells with 0.1% Trypsin/EDTA treatment for 15 min at 37 °C with periodic pipetting. After the reaction was quenched by adding an equal volume of FBS strained through a 70 μm nylon cell strainer, cells were resuspended in FACS buffer (0.1% BSA in PBS). Cells were loaded into chromium microfluidic chips with the Chromium Next GEM Single Cell 3ʼReagent Kit (v3.1 chemistry) and then used to generate single-cell gel bead emulsions (GEMs) using the Chromium Controller (10× Genomics) according to the manufacturer’s protocol. GEM-RT was performed in a C1000 Touch Thermal Cycler with 96-Deep Well Reaction Module (Bio-Rad). All subsequent cDNA amplification and library construction steps were performed according to the manufacturer’s protocol. Libraries were sequenced using a 2 × 150 paired-end sequencing protocol on an Illumina HiSeq 4000 or NovaSeq 6000 instrument.
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|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic single cell |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 4000 |
|
|
Data processing |
The demultiplexing, barcoded processing, gene counting and aggregation were made using the Cell Ranger software v.6.0.1 (https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/what-is-cell-ranger). Assembly: calJac4 Supplementary files format and content: h5 files of row counts tables.
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|
|
Submission date |
Jul 27, 2022 |
Last update date |
Feb 17, 2023 |
Contact name |
keren cheng |
E-mail(s) |
keren.cheng@outlook.com
|
Organization name |
Zhejiang University
|
Department |
School of Medicine
|
Street address |
1575 chouzhou bei road
|
City |
Yiwu |
State/province |
Zhejiang |
ZIP/Postal code |
320000 |
Country |
China |
|
|
Platform ID |
GPL26566 |
Series (2) |
GSE209932 |
Efficient generation of marmoset primordial germ cell-like cells using induced pluripotent stem cells [scRNA-seq] |
GSE210576 |
Efficient generation of marmoset primordial germ cell-like cells using induced pluripotent stem cells |
|
Relations |
BioSample |
SAMN30004726 |
SRA |
SRX16702103 |