|
Status |
Public on Jul 08, 2020 |
Title |
SRSF1_IM_rep2 |
Sample type |
SRA |
|
|
Source name |
ATCC
|
Organism |
Homo sapiens |
Characteristics |
origin: Human-derived blast crisis CML cell line cell line: K562
|
Treatment protocol |
Transduced cells were treated for 48 h with 0.5uM imatinib
|
Growth protocol |
K562 cells were obtained commercially from ATCC and maintained in RPMI supplemented with 10% FBS and 1% pen-strep. Cells were transduced with virus packaging either the SRSF1 gene or an empty vector control
|
Extracted molecule |
total RNA |
Extraction protocol |
Suspension cells were harvested by centrifugation. RNA was extracted with the Qiagen RNeasy mRNA kits following manufacturer's instructions Only RNA with RIN>7 was used. Library prep was performed using the illumina Truseq Stranded Total RNA kit with Ribozero Gold. Each experimental condition for RNA-seq was performed in triplicate, each at a sequencing depth of 50M reads. RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
RNA-seq aligned to hg19 genome and UCSC refrence transcript with STAR(version 2.4.0). Bigwig files are converted by bedGraphToBigWig from bedGraph generted by bedtools. Genome_build: hg19 Supplementary_files_format_and_content: bigwig
|
|
|
Submission date |
Nov 13, 2019 |
Last update date |
Jul 08, 2020 |
Contact name |
Jia Li |
Organization name |
Duke-NUS
|
Street address |
8 College Road
|
City |
Singapore |
ZIP/Postal code |
169857 |
Country |
Singapore |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE140322 |
Transcriptomic analysis of SRSF1 overexpression and imatinib treatment in K562 CML cell lines |
|
Relations |
BioSample |
SAMN13279748 |
SRA |
SRX7135357 |