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SRX9728574: GSM4982811: MULTIseq Sample A; Homo sapiens; RNA-Seq
2 ILLUMINA (HiSeq X Ten) runs: 520.8M spots, 158.7G bases, 73.2Gb downloads

Submitted by: NCBI (GEO)
Study: Multiplexed single cell mRNA sequencing of monolayer- and organoid-system differentiated cells derived from human iPSC with and without NKX2-5 genetic manipulations
show Abstracthide Abstract
Three wild type cell lines (WTC:ACTN2-eGFP, WTC:Myl2-eGFP, SCVI114) and three genetically modified cell lines (PM28, PM52, Del33) were differentiated using two monolayer (atrial and ventricular) and two organoid (also atrial and ventricular) differentiation protocols. Cells from multiple samples at differentiation day 15 (wild type cell lines) and day 30 (all cell lines) were isolated, multiplexed using the MULTI-seq approach; subsequently library preparation (10X platform) and sequencing was performed. Overall design: Single cell sequencing of wild type and Nkx2-5 genetically modified hiPSC derived cells using monolayer and organoid systems at day15 and day30
Sample: MULTIseq Sample A
SAMN17128295 • SRS7921401 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cardiac cells from monolayer differentiation culture at day 15 and day 30 were dissociated with TrypLE and washed once with HBSS-/- (Ca2+/Mg2+ free). The cardiac organoids were sequencially incubated with 0.25% Trypsin/EDTA and a collagenase HBSS+/+ mixture before filtered through a 40 μm filter. The cells from each sample were stained with with a unique MULTI-seq barcode separately and pooled before library preparation. The pooled cells were captured in 10X Chromium (10X Genomics, 120223) by following the single cell 3' reagent kits v3 user guide. Briefly, cells were loaded into each chip well to be partitioned into gel beads in emulsion (GEMs) in the Chromium controller. We targeted for 25,000 cells in each chip well and profiled one well for the first batch experiment and two chip wells for the second experiment. The cells were then lysed and barcoded reverse transcribed in the GEMs. After breaking the GEMs and further cleanup and amplification, the cDNA was enzymatically fragmented and 3′ end fragments were selected for library preparation. After further processing including end repair, A-tailing, adaptor ligation, and PCR amplification, a string of sequences including sample index, UMI sequences, barcode sequences, and sequencing primer P5 and P7 were added to cDNA on both ends. The libraries were sequenced on Illumina HiSeq X platform.
Experiment attributes:
GEO Accession: GSM4982811
Links:
Runs: 2 runs, 520.8M spots, 158.7G bases, 73.2Gb
Run# of Spots# of BasesSizePublished
SRR13299641302,033,60293G42.3Gb2022-05-05
SRR13299642218,789,24765.6G30.9Gb2022-05-05

ID:
12721608

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