Author

Sebastian Knöbel

Miltenyi Biotec (Germany)ORCID 0000-0001-9965-5557Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:ATAC-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1

Frequent Co-Authors

Hannah Johannsen· 2 shared Andreas BosioiD· 1 shared Andreas DahliD· 1 shared Andreas PetzoldiD· 1 shared Anja FeldmanniD· 1 shared Anne SchöniD· 1 shared Annett Kurtz· 1 shared Annika Last· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersCell Biology

Hannah Johannsen

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintSep 5, 2026

Minimizing time in culture: A prototypic autologous manufacturing workflow for monoclonal iPSC lines within seven weeks

Diana Haberhausen, Christian Woehle, Constanze Raab…·Sebastian Knöbel

This study develops a time-efficient, standardizable workflow for generating monoclonal iPSC lines from human skin biopsies within seven weeks, with low variability and genomic integrity.

DOI 10.64898/2026.08.04.741960

humanATAC-seq

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NeurosciencebioRxivPreprintOct 15, 2024

Extensive monolayer formation after transplantation depends on a RPE subpopulation derived from human iPSCs

Karen Tessmer, Sylvia Jane Gasparini, Klara Schmidtke…·Marius Ader

The paper shows that passage 1 human iPSC-derived RPE cells form more extensive monolayers after transplantation compared to passage 2 cells, highlighting a subpopulation with higher transplantation potential.

1 citation

mousebulk RNA-seq

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