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@ARTICLE{Kotowicz:279428,
author = {Kotowicz, Malwina and Shumanska, Magdalena and Fengler,
Sven and Kurkowsky, Birgit and Meyer-Berhorn, Anja and
Moretti, Elisa and Blersch, Josephine and Schmidt, Gisela
and Kreye, Jakob and van Hoof, Scott and Sánchez-Sendín,
Elisa and Reincke, S Momsen and Krüger, Lars and Prüß,
Harald and Denner, Philip and Fava, Eugenio and Stappert,
Dominik},
title = {{G}ain efficiency with streamlined and automated data
processing: {E}xamples from high-throughput monoclonal
antibody production.},
journal = {PLOS ONE},
volume = {20},
number = {7},
issn = {1932-6203},
address = {San Francisco, California, US},
publisher = {PLOS},
reportid = {DZNE-2025-00759},
pages = {e0326678 -},
year = {2025},
abstract = {Data management and sample tracking in complex biological
workflows are essential steps to ensure necessary
documentation and guarantee reusability of data and
metadata. Currently, these steps pose challenges related to
correct annotation and labeling, error detection, and
safeguarding the quality of documentation. With growing
acquisition of biological data and the expanding
automatization of laboratory workflows, manual processing of
sample data is no longer favorable, as it is time- and
resource-consuming, prone to biases and errors, and lacks
scalability and standardization. Thus, managing
heterogeneous biological data calls for efficient and
tailored systems, especially in laboratories run by
biologists with limited computational expertise. Here, we
showcase how to meet these challenges with a modular
pipeline for data processing, facilitating the complex
production of monoclonal antibodies from single B-cells. We
present best practices for development of data processing
pipelines concerned with extensive acquisition of biological
data that undergoes continuous manipulation and analysis.
Moreover, we assess the versatility of proposed design
principles through a proof-of-concept data processing
pipeline for automated induced pluripotent stem cell culture
and differentiation. We show that our approach streamlines
data management operations, speeds up experimental cycles
and leads to enhanced reproducibility. Finally, adhering to
the presented guidelines will promote compliance with FAIR
principles upon publishing.},
keywords = {Antibodies, Monoclonal: biosynthesis / Humans / Animals /
Induced Pluripotent Stem Cells: cytology / Induced
Pluripotent Stem Cells: metabolism / B-Lymphocytes:
immunology / B-Lymphocytes: cytology / B-Lymphocytes:
metabolism / Reproducibility of Results / High-Throughput
Screening Assays: methods / Cell Differentiation / Workflow
/ Automation / Antibodies, Monoclonal (NLM Chemicals)},
cin = {LAT / LIS / AG Prüß / Tech Transfer / CRFS},
ddc = {610},
cid = {I:(DE-2719)1040190 / I:(DE-2719)1040260 /
I:(DE-2719)1810003 / I:(DE-2719)1030028 /
I:(DE-2719)1040000},
pnm = {899 - ohne Topic (POF4-899) / 353 - Clinical and Health
Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-899 / G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40591905},
doi = {10.1371/journal.pone.0326678},
url = {https://pub.dzne.de/record/279428},
}