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Sample GSM3349770 Query DataSets for GSM3349770
Status Public on Jul 03, 2019
Title RNA-seq_III-3-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/Corr-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 Isogenic line to III-3 to correct LMNA mutation
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 SAMN09873820
SRA SRX4590584

Supplementary file Size Download File type/resource
GSM3349770_RNA_PT3WT_Rep1Aligned.out.sorted.q255.bw 72.9 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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