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Johanna Geuder

Researcher at Ludwig Maximilian University of Munich

Publications -  9
Citations -  208

Johanna Geuder is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Biology & Induced pluripotent stem cell. The author has an hindex of 3, co-authored 6 publications receiving 112 citations.

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Sensitive and powerful single-cell RNA sequencing using mcSCRB-seq

TL;DR: This work systematically evaluates experimental conditions of this protocol and finds that adding polyethylene glycol considerably increases sensitivity by enhancing cDNA synthesis and using Terra polymerase increases efficiency due to a more even cDNA amplification that requires less sequencing of libraries.
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A non-invasive method to generate induced pluripotent stem cells from primate urine

TL;DR: In this article, the authors reported the generation of primate induced pluripotent stem cells (iPSCs) from urine samples and showed that suspension-sendai virus transduction of reprogramming factors into urinary cells efficiently generates integration-free iPSCs which maintain their pluripotency under feeder-free culture conditions.
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Prime-seq, efficient and powerful bulk RNA sequencing

TL;DR: In this paper , the authors optimize and validate prime-seq, an early barcoding bulk RNA-seq method, and show that it performs equivalently to TruSeq, but is four times more cost-efficient due to almost 50 times cheaper library costs.
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A non-invasive method to generate induced pluripotent stem cells from primate urine

TL;DR: This study introduces a novel and efficient approach to generate iPSCs non-invasively from primate urine, which will allow to extend the zoo of species available for a comparative approach to molecular and cellular phenotypes.
Posted ContentDOI

mcSCRB-seq: sensitive and powerful single-cell RNA sequencing

TL;DR: Adding polyethylene glycol considerably increases sensitivity and using Terra polymerase increases efficiency due to a more even cDNA amplification that requires less sequencing of libraries, combined with other improvements to a new scRNA-seq library protocol, which is shown to be the most sensitive and one of the most efficient and flexible sc RNA-seq methods to date.