|
Status |
Public on Apr 25, 2022 |
Title |
ADAR1 Ctrl cell line |
Sample type |
SRA |
|
|
Source name |
IMR90 cell llines
|
Organism |
Homo sapiens |
Characteristics |
adar1 status: Ctrl cell line: IMR90
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated from cells using RNeasy mini kit (Qiagen, 74106) and digested with DNase I (Qiagen, 79254). The libraries were prepared using a KAPA RNA HyperPrep kit (cat. no. Roche, Cat. no: 07962312001)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
ADAR1 Ctrl cell line
|
Data processing |
RNA-Seq data analysis was done with rsem (ver. 1.2.3) and hg19 genome with ensemble transcriptome information to estimate raw counts and FPKM values DESeq2 was used for normalization Genome_build: hg19 Supplementary_files_format_and_content: Prosessed files contains the raw counts and FPKM for each gene
|
|
|
Submission date |
Jul 04, 2021 |
Last update date |
Apr 25, 2022 |
Contact name |
Priyankara J Wickramasinghe |
E-mail(s) |
priyaw@wistar.org
|
Phone |
2154956837
|
Organization name |
The Wistar Institute
|
Department |
Bioinformatics
|
Lab |
Genomics
|
Street address |
3601 Spruce Street
|
City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (1) |
GSE179423 |
ADAR1 downregulation contributes to p16INK4a upregulation independent of RNA editing during senescence |
|
Relations |
BioSample |
SAMN20057203 |
SRA |
SRX11349277 |