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Background Induced pluripotent stem cells (iPSCs) derived from dilated cardiomyopathy (DCM) patients offer an unprecedented platform for in vitro disease modeling[1]. Time course transcriptome analysis on the differentiation process from iPSCs to beating cardiomyocytes will reveal the holistic dynamic gene expression landscapes and pinpoint molecular deficiencies in cardiogenesis for DCM patients.

Time course transcriptome data analysis for in vitro modeling of dilated cardiomyopathy using patient-derived induced pluripotent stem cells