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Maier, H.

Publications and source records attributed to Maier, H..

2 recordsLinked to original sources

FERDINAND: An Open Framework for Download and AI-ready Preprocessing of IMPC 2D Radiographs

The International Mouse Phenotyping Consortium (IMPC) maintains a large archive of whole-body dorsoventral radiographs. However, heterogeneity in file formats, metadata completeness, orientation, and image quality limits its reuse for large-scale quantitative analysis. We present FERDINAND (Framework for Extracting and Restructuring Distributed IMPC radiographs into a Normalised, AI-ready Navigable Dataset), an open framework for programmatic access, harmonisation, quality control, and curation of IMPC radiographs. FERDINAND combines metadata retrieval and local radiograph archiving with centre-aware preprocessing, automated exposure screening, orientation standardisation, and clustering-assisted visual curation. Applied to IMPC Data Release 24, FERDINAND organises 104,819 radiographs acquired between February 2012 and June 2025 across ten phenotyping centres and 6,306 single-gene knockout mouse lines, with semi-automated curation recorded for every image. As an independent validation of the harmonised output, a DeepLabCut-based bone-morphometry pipeline showed that FERDINAND-processed radiographs improve data efficiency for landmark detection: at reduced training-set sizes, they achieve better performance than original radiographs and require fewer manual annotations to reach a given level of quality. FERDINAND provides a reproducible foundation for artificial intelligence (AI)-ready analysis and scalable quantitative phenotyping of heterogeneous IMPC and comparable radiograph resources. The complete FERDINAND source code is openly available on GitHub.

bioinformatics↗

The porcine deltacoronavirus replication organelle comprises double membrane vesicles and zippered endoplasmic reticulum with double membrane spherules

Porcine deltacoronavirus (PDCoV) was first identified in Hong Kong in 2012 from samples taken from pigs in 2009. PDCoV was subsequently identified in the USA in 2014 in pigs with a history of severe diarrhea and the virus has now been detected in pigs in several countries around the world. Following the development of tissue culture adapted strains of PDCoV, it is now possible to begin to address questions regarding virus-host cell interactions for this genera of coronavirus. Here we present a detailed study of PDCoV induced replication organelles. All positive strand RNA viruses induce the rearrangement of cellular membranes during virus replication to support viral RNA synthesis, forming the replication organelle. Replication organelles for the Alpha-, Beta- and Gammacoronavirus genera have been characterized. However the structures induced by deltacoronaviruses, in particular the presence of convoluted membranes or double membrane spherules, are unknown. Initially, the dynamics of PDCoV strain OH-FD22 replication were assessed with the onset of viral RNA synthesis, protein synthesis and progeny particle release determined. Subsequently, virus induced membrane rearrangements were identified in infected cells by electron microscopy. As has been observed for all other coronaviruses studied to date, PDCoV replication was found to induce the formation of double membrane vesicles. Significantly however, PDCoV replication was also found to induce the formation of regions of zippered endoplasmic reticulum and small associated tethered vesicles, double membrane spherules. These structures strongly resemble the replication organelle induced by avian Gammacoronavirus infectious bronchitis virus.

microbiology↗