Single cell transcriptomes of hPSC-derived skeletal muscle progenitor cells (SMPCs; MP subpopulations from the myogenic subsets) obtained using three different protocols (HX protocol, Xi et al., Cell Rep, 2017; JC protocol, Chal et al., Nat Biotechnol, 2015; MS protocol, Shelton et al., Stem Cell Rep, 2014) are aligned to human prenatal SMPCs and postnatal juvenile […]
Single cell transcriptomes of hPSC-derived skeletal muscle progenitor cells (SMPCs; MP subpopulations from the myogenic subsets) obtained using the HX protocol (Xi et al., Cell Rep, 2017) at different time points of differentiation are aligned to human prenatal SMPCs and postnatal juvenile and adult skeletal muscle stem cells (satellite cells; SCs). SMPCs generated from hPSCs […]
Single cell transcriptomes of prenatal skeletal muscle progenitor cells (SMPCs; MP subpopulations from the myogenic subsets) from different stages of embryonic and fetal development as well as postnatal juvenile and adult skeletal muscle stem cells (satellite cells; SCs) are combined into a single dataset. The developmental trajectory of SMPCs and SCs are analyzed using diffusion […]
Single cell transcriptomes of the skeletal muscle (SkM) lineage from human pluripotent stem cell (hPSCs) differentiated for 6-7 weeks using the MS protocol (Shelton et al., Stem Cell Rep, 2014). Cells are subjected to re-clustering to reveal potential heterogeneity within the myogenic subset.
Single cell transcriptomes of cell cultures differentiated from human pluripotent stem cells (hPSCs) following the MS protocol (Shelton et al., Stem Cell Rep, 2014) for 6-7 weeks. Cells are either non-enriched, or enriched using an endogenous PAX7-driven GFP reporter or cell surface marker combination of ERBB3+NGFR+HNK1-.
Single cell transcriptomes of the skeletal muscle (SkM) lineage from human pluripotent stem cell (hPSCs) differentiated for 5 weeks using the JC protocol (Chal et al., Nat Biotechnol, 2015). Cells are subjected to re-clustering to reveal potential heterogeneity within the myogenic subset.
Single cell transcriptomes of cell cultures differentiated from human pluripotent stem cells (hPSCs) following the JC protocol (Chal et al., Nat Biotechnol, 2015) for 5 weeks. Cells are either non-enriched, or enriched using an endogenous PAX7-driven GFP reporter or cell surface marker combination of ERBB3+NGFR+HNK1-.
Single cell transcriptomes of the skeletal muscle (SkM) lineage from human pluripotent stem cell (hPSCs) differentiated for 8 weeks using the HX protocol (Xi et al., Cell Rep, 2017). Cells are subjected to re-clustering to reveal potential heterogeneity within the myogenic subset.
Single cell transcriptomes of cell cultures differentiated from human pluripotent stem cells (hPSCs) following the HX protocol (Xi et al., Cell Rep, 2017) for 8 weeks. Cells are either non-enriched or enriched using an endogenous PAX7-driven GFP reporter.
Single cell transcriptomes of the skeletal muscle (SkM) lineage from human pluripotent stem cell (hPSCs) differentiated for 6 weeks using the HX protocol (Xi et al., Cell Rep, 2017). Cells are subjected to re-clustering to reveal potential heterogeneity within the myogenic subset.