|
Status |
Public on Jul 03, 2019 |
Title |
RNA-seq_IV-1-WT, rep1 |
Sample type |
SRA |
|
|
Source name |
iPSC-CMs
|
Organism |
Homo sapiens |
Characteristics |
cell type: iPSC-CMs day post-differentiation: day 40 genotype/variation: LMNA WT/WT
|
Treatment protocol |
iPSCs were grown to 90% confluence and subsequently differentiated into beating cardiomyocytes, using a small-molecule-based monolayer method described previously. Ten days after cardiac differentiation, iPSC-CM monolayers were purified using RPMI-1640 without glucose (Life Technologies) with B27 supplement (Life Technologies). Non-glucose culture medium was changed every 2 days. After 5 days, iPSC-CMs were reseeded onto Matrigel-coated plates in a culture medium containing glucose.
|
Growth protocol |
iPSC lines were maintained in chemically defined medium Essential 8 (E8 medium) (Life Technologies) on Matrigel-coated (BD Bioscience, San Jose, CA) plates at 37°C with 5% (vol/vol) CO2.
|
Extracted molecule |
total RNA |
Extraction protocol |
iPSC-CMs were detached from cell culture plates and RNA was extracted using a microRNeasy kit (QIAGEN). RNA libraries were prepared for sequencing using standard Illumina protocols.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
NextSeq 550 |
|
|
Description |
Parental line IV-1 RNA-seq Replicate #1
|
Data processing |
Base quality of raw reads: FastQC 0.11.4 Aligned the reads to the human reference genome (hg19): STAR 2.5.1b Calculating fragments per kilobase per million aligned reads (FPKM): Cufflinks 2.2.1 Genome_build: human reference genome hg19 (GRCh37) Supplementary_files_format_and_content: bigWig
|
|
|
Submission date |
Aug 21, 2018 |
Last update date |
Jul 03, 2019 |
Contact name |
Lei Tian |
E-mail(s) |
[email protected]
|
Phone |
6502388262
|
Organization name |
Stanford's Postdoctoral Scholar programs
|
Street address |
1215 Welch Rd
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
|
|
Platform ID |
GPL21697 |
Series (2) |
GSE118882 |
Dysregulation of PDGFRB contributes to the pathogenesis of LMNA-related dilated cardiomyopathy [RNA-seq] |
GSE118885 |
Dysregulation of PDGFRB contributes to the pathogenesis of LMNA-related dilated cardiomyopathy |
|
Relations |
BioSample |
SAMN09873824 |
SRA |
SRX4590588 |