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@ARTICLE{Kotowicz:266775,
author = {Kotowicz, Malwina and Fengler, Sven and Kurkowsky, Birgit
and Meyer-Berhorn, Anja and Moretti, Elisa and Blersch,
Josephine and Shumanska, Magdalena and Schmidt, Gisela and
Kreye, Jakob and Hoof, Scott and Sánchez-Sendín, Elisa and
Reincke, 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 = {bioRxiv beta},
address = {Cold Spring Harbor},
publisher = {Cold Spring Harbor Laboratory, NY},
reportid = {DZNE-2024-00038},
year = {2023},
abstract = {Data management and sample tracking in complex biological
workflows are essential steps to ensure necessary
documentation and guarantee the 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
samples is no longer favorable, as it is time- and
resource-consuming, is 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.},
cin = {LAT / LIS / Tech Transfer / AG Prüß / AG Fava},
ddc = {570},
cid = {I:(DE-2719)1040190 / I:(DE-2719)1040260 /
I:(DE-2719)1030028 / I:(DE-2719)1810003 /
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)25},
doi = {10.1101/2023.12.14.571214},
url = {https://pub.dzne.de/record/266775},
}