Human induced pluripotent stem cell-derived neural progenitor cells (NPCs) provide a controlled in-vitro model for studying early stages of neuronal differentiation. Here, we present a multimodal single-cell dataset generated from NPCs differentiated over four time points (days 0, 7, 13 and 20) under baseline conditions and following exposure to amyloid-β (Aβ) 1-42 peptide. The dataset comprises paired single-cell RNA sequencing (scRNA-seq) and single-cell ATAC sequencing (scATAC-seq) profiles, enabling joint characterization of transcriptional and chromatin accessibility dynamics during differentiation. Following stringent quality control, we analyzed 42575 and 30192 high-quality cells for RNA and ATAC respectively, providing an in-depth characterization of cell composition, molecular signaling pathways, functional properties, and gene regulatory network annotations. To facilitate reuse and benchmarking, transcriptional signatures derived from this dataset were additionally compared with a publicly available human hippocampal bulk RNA-seq dataset. This resource provides a reference multimodal dataset for human NPC-derived neuronal differentiation and supports a broad range of single-cell, multimodal integration, and regulatory network analyses.
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Idoia Blanco-Luquin
Navarrabiomed
Xabier Martínez-de-Morentin
King Abdullah University of Science and Technology
Amaia Amaia Vilas-Zornoza
Navarre Institute of Health Research
Scientific Data
Karolinska Institutet
Queen Mary University of London
Karolinska University Hospital
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Blanco-Luquin et al. (Tue,) studied this question.
synapsesocial.com/papers/69b3aaa802a1e69014ccb7bc — DOI: https://doi.org/10.1038/s41597-026-06971-4
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