|
Status |
Public on Feb 05, 2021 |
Title |
P1 cortex single cell RNA-seq |
Sample type |
SRA |
|
|
Source name |
mouse cortex
|
Organism |
Mus musculus |
Characteristics |
strain: CD1 age: P1 tissue: cortex
|
Treatment protocol |
IS mouse were electroperated with pCAG-Cre plasmid and the cortex were harvested at P1 through FACS for scRNA-seq. For scATAC-seq, GFP+ cell were from FACS sorted E18.5 hGFAP-GFP cortex.
|
Extracted molecule |
total RNA |
Extraction protocol |
Chromium single cell ATAC library and single cell RNA libraries were prepared for sequencing using standard 10X genomics protocols single cell RNA-seq and single cell ATAC-seq
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
sc ATAC-seq: Cell ranger-ATAC pipeline software was used for base-calling, and alignment. SCALE pipeline was used for filtering, ZINBA software was used for peak calling ScRNA-seq: Cell ranger pipeline was used for base-calling, aligment and filtering. Seurat was used for further analyse. Genome_build: mm10 Supplementary_files_format_and_content: matrix data containing raw counts for all cells in scRNA-seq raw peaks for all single cells for scATAC-seq data
|
|
|
Submission date |
Nov 09, 2020 |
Last update date |
Feb 09, 2021 |
Contact name |
Guoping Liu |
E-mail(s) |
gpliu@fudan.edu.cn
|
Phone |
18521006300
|
Organization name |
Fudan University
|
Street address |
138 Yi Xue Yuan Road
|
City |
Shanghai |
ZIP/Postal code |
200032 |
Country |
China |
|
|
Platform ID |
GPL24247 |
Series (1) |
GSE161132 |
Decoding Cortical Glial Cell Development |
|
Relations |
BioSample |
SAMN16710098 |
SRA |
SRX9463246 |