|
Status |
Public on Nov 08, 2022 |
Title |
Control_singlecell_rep1 |
Sample type |
SRA |
|
|
Source name |
Retina
|
Organism |
Oryctolagus cuniculus |
Characteristics |
condition: Control cell type: retinal cells
|
Extracted molecule |
total RNA |
Extraction protocol |
Papain dissociation to prepare single cell suspension or 0.01% Nonidet P40 lysis buffer to prepare single nuclei suspension scRNA-Seq following 10x ver3.1 guideline
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic single cell |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
scRNA-Seq: Sequencing results were processed through the Cell Ranger pipeline (10x Genomics) with default parameters. Seurat V3 was used to perform downstream analysis following the standard pipeline. Assembly: OryCun2.0
|
|
|
Submission date |
Nov 04, 2022 |
Last update date |
Nov 08, 2022 |
Contact name |
Clayton Pio Santiago |
E-mail(s) |
csanti10@jhmi.edu
|
Organization name |
Johns Hopkins University
|
Department |
Neuroscience
|
Street address |
733 North Broadway
|
City |
Baltimore |
State/province |
Maryland |
ZIP/Postal code |
21205 |
Country |
USA |
|
|
Platform ID |
GPL26786 |
Series (1) |
GSE217333 |
Comparative analysis of single-cell and single-nucleus RNA-sequencing in a rabbit model of retinal detachment-related proliferative vitreoretinopathy |
|
Relations |
BioSample |
SAMN31611924 |
SRA |
SRX18175233 |