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Gronning, A. G. B.

Publications and source records attributed to Gronning, A. G. B..

2 recordsLinked to original sources

PepHammer - a lightweight web-based tool for bioactive peptide matching and identification

Peptides are gaining increasing attention as therapeutic agents. Already, peptide-based therapeutics play a key role in the treatment of diverse diseases, including diabetes, obesity, and other complex disorders, and their clinical relevance is expected to expand further in the coming years. Technological and computational advances have substantially enriched peptidomics, massively increasing the scale and depth of peptide identification. As a result, increasingly large and information-rich datasets are now available for downstream analysis and experimental validation. However, the rapid expansion of peptidomics datasets also leads to a corresponding increase in search space, complicating the efficient identification of peptides relevant to specific biological or clinical questions. To address this challenge, we present PepHammer, a lightweight web-based tool for bioactive peptide matching and identification. PepHammer allows users to input up to 10000 peptides (2-150 amino acids in length) and compare them against extensive databases of peptides with predicted or experimentally validated bioactivities and tissue associations using Hamming distance, Grantham distance, as well as partial or exact matching strategies. Via an example study of human milk peptidomics, we demonstrate that PepHammer rapidly provides an overview of the bioactivity and tissue-relational landscape, serving as a starting point for downstream analyses. PepHammer thus enables efficient exploration of large-scale peptidomics datasets and facilitates the identification of biologically relevant peptides.

bioinformatics↗

BioTrendFinder - an interactive web tool for exploring functional drivers in gene- and protein-level bulk omics data

The analysis of bulk omics data, such as RNA-seq and proteomics, has enabled numerous biological discoveries. Standard analytical workflows typically comprise dimensionality reduction, group-wise statistical comparisons, functional enrichment analysis, and mapping of molecules to biological networks. Although informative, these steps are often applied independently, limiting integrative interpretation and the efficient identification of functional drivers and candidate targets. To address these limitations, we developed BioTrendFinder, an interactive web tool for exploring functional drivers in gene- and protein-level bulk omics data. BioTrendFinder employs a sample-ranking strategy to identify significant molecular trendlines that capture expression patterns across ranked sample compositions in dimensionally reduced data. These trends are integrated with statistical results, sample-group metadata and functional information from STRING and eleven bio-ontologies, enabling interactive network-based exploration and the generation of entity-ranked functional modules. BioTrendFinders unique approach and functionalities add additional analytical dimensions to bulk omics data by facilitating the extraction of high-level information from alternative analytical perspectives. Using previously published proteomics and transcriptomics datasets, we demonstrate that BioTrendFinder supports both hypothesis-driven and exploratory investigations, enabling the prioritization of candidate molecular targets and effectively narrowing the search space for downstream validation steps.

bioinformatics↗