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Zielinski, T.

Publications and source records attributed to Zielinski, T..

3 recordsLinked to original sources

The Shape of Biological Metadata: Measuring Repository Richness with Entity-Based NLP Metrics

Ensuring the availability and accessibility of research data is fundamental to advancing knowledge, as codified in the FAIR principles (Findable, Accessible, Interoperable, and Reusable). Accurate metadata documentation is indispensable for meeting these principles; however, entries in deposition databases often contain inadequate, repetitive, or incomplete descriptions. Much of this metadata is captured in free-text fields, motivating the need for scalable, repository-agnostic methods to quantify metadata richness. Here, we quantify free-text metadata richness across three repositories using Natural Language Processing (NLP) methods: BioDare2, an experimental circadian rhythm database; DataShare, a domain-agnostic University of Edinburgh database; and Image Data Resource (IDR), a public repository of biological image datasets from published studies. In general, repositories exhibit distinct distributions of word count and information density, consistent with differences in scope. Named-entity recognition and information-density metrics detected significant category-level differences in BioDare2 (species) and DataShare (communities), while identifying greater consistency in the more curated IDR. The most frequent entities reflected each repository's focus: circadian terminology in BioDare2, microscopy-related entities in IDR, and community-driven terms in DataShare. We develop a scalable framework utilising word counts, named-entity recognition, and entity-derived information density to assess metadata quality across repositories, offering a broadly applicable evaluation tool.

bioinformatics↗

A Decade of Progress: Insights of Open Data Practices in Biosciences at the University of Edinburgh

Open science promotes the accessibility of scientific research and data, emphasising transparency, reproducibility, and collaboration. This study assesses the openness and FAIRness (Findable, Accessible, Interoperable, and Reusable) of data-sharing practices within the biosciences at the University of Edinburgh from 2014 to 2023. We analysed 555 research papers across biotechnology, regenerative medicine, infectious diseases, and non-communicable diseases. Our scoring system evaluated data completeness, reusability, accessibility, and licensing, finding a progressive shift towards better data-sharing practices. The fraction of publications that share all relevant data increased significantly, from 7% in 2014 to 45% in 2023. Data involving genomic sequences were shared more frequently than image data or data on human subjects or samples. The presence of data availability statement (DAS) or preprint sharing correlated with more and better data sharing, particularly in terms of completeness. We discuss local and systemic factors underlying the current and future Open data sharing. Evaluating the automated ODDPub (Open Data Detection in Publications) tool on this manually-scored dataset demonstrated high specificity in identifying cases where no data was shared. ODDPub sensitivity improved with better documentation in the DAS. This positive trend highlights improvements in data-sharing, advocating for continued advances and addressing challenges with data types and documentation.

bioinformatics↗

Changes in nanomechanical properties of single neuroblastoma cells as a model for oxygen and glucose deprivation (OGD)

The biological processes underlying ischemic stroke, although complex, are better known than those related to biomechanical alterations of single cells. Mechanisms of biomechanical changes and their relations to the molecular processes are crucial for understanding the function and dysfunction of the brain. In our study, we applied atomic force microscopy (AFM) to quantify the alterations in biomechanical properties in neuroblastoma SH-SY5Y cells subjected to oxygen and glucose deprivation (OGD) and reoxygenation (RO). Obtained results reveal several characteristics. Cell viability remained at the same level, regardless of the OGD and RO conditions, but, in parallel, the metabolic activity of cells decreased with OGD duration. 24h RO did not recover the metabolic activity fully. Cells subjected to OGD appeared softer than control cells. Cell softening was strongly present in cells after 1h of OGD and, with longer OGD duration and in RO conditions, cells recovered their mechanical properties. Changes in the nanomechanical properties of cells were attributed to the remodelling of actin filaments, which was related to cofilin-based regulation and impaired metabolic activity of cells. The presented study shows the importance of nanomechanics in research on ischemic-related pathological processes such as stroke.

biophysics↗