|
Status |
Public on Sep 24, 2020 |
Title |
PEER DAC Rep3 RNA-seq |
Sample type |
SRA |
|
|
Source name |
T-ALL cell line PEER
|
Organism |
Homo sapiens |
Characteristics |
cell line: PEER treatment: Decitabine tissue: T-ALL cell line
|
Treatment protocol |
Cell lines were treated with 1μM Decitabine or DMSO control for 48h
|
Growth protocol |
Cell lines were cultured in RPMI-1640 medium supplemented with 10 or 20% fetal calf serum, 100 U/ml penicillin, 100 µg/ml streptomycin, and 2 mM L-glutamine at 37°C with 5% CO2.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA extraction was performed using the miRNeasy Mini Kit (Qiagen). RNA sequencing libraries were prepared using the QuantSeq 3’ mRNA-Seq Library Prep FWD kit (Lexogen)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
RNA sequencing reads were aligned to GRCh38 using STAR (version 2.4.2a)42 and quantified on Gencode v24. Normalization of counts was done using DESeq2. Genome_build: hg38
|
|
|
Submission date |
Jul 29, 2020 |
Last update date |
Sep 24, 2020 |
Contact name |
Juliette Roels |
E-mail(s) |
roels.juliette@gene.com
|
Phone |
6505807476
|
Organization name |
Genentech
|
Street address |
1 DNA Way
|
City |
South San Francisco |
State/province |
CA |
ZIP/Postal code |
94080 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (2) |
GSE155337 |
Aging of preleukemic thymocytes drives CpG island hypermethylation in T-cell acute lymphoblastic leukemia [RNAseq_DAC_celllines] |
GSE155339 |
Aging of preleukemic thymocytes drives CpG island hypermethylation in T-cell acute lymphoblastic leukemia |
|
Relations |
BioSample |
SAMN15666615 |
SRA |
SRX8843182 |