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Stiller, W.

Publications and source records attributed to Stiller, W..

2 recordsLinked to original sources

Novel linkage disequilibrium-based genotype-by-environmental interaction method for genomic prediction of cotton yield and fibre quality traits

Genomic prediction (GP) across diverse environments has a potential to accelerate genetic gain in cotton breeding programs. A major challenge in GP is modelling genotype-by-environment interactions (GEI), which is essential for selecting stable and high-performing genotypes under variable production conditions. However, incorporating GEI into GP models increases the dimensionality and computational complexity, risking complex models that are impractical to use on commercial breeding-scale data sets because of run times and computational demands. This study addresses two primary aims. Firstly, we evaluate the practical benefits of GEI-informed GP for predicting economically important cotton traits. Second, advanced statistical modelling strategies are developed and assessed for integrating genomic and environmental data at scale. We propose a dimensionality reduction approach that combines linkage disequilibrium network analysis with principal component techniques to reduce redundancy while preserving informative variation. Using this reduced dataset, we implement Bayesian linear regression models and, for comparison, deep residual neural networks for genomic prediction. Analyses were conducted on a large multi-environment dataset from the CSIRO cotton breeding program, comprising 3,236 breeding lines, 54 environmental covariates, and 8,049 yield and fibre quality phenotype records collected over 10 years and 9 locations representing 41 year-location combinations. Results demonstrate that generally Bayesian linear regression approaches outperform BG-BLUP models, with all three linear/linear mixed methods providing clearly more reliable performance than the deep learning models. These findings highlight the value of using interpretable statistical models for integrating genomic and environmental information to support selection decisions under diverse environmental conditions.

plant biology↗

Longitudinal Micro-Computed Tomography Detects Onset and Progression of Pulmonary Fibrosis in Conditional Nedd4-2 Deficient Mice

ObjectivesIdiopathic pulmonary fibrosis (IPF) is a fatal lung disease which is usually diagnosed late in advanced stages. Little is known about the subclinical development of IPF. We previously generated a mouse model with conditional Nedd4-2 deficiency (Nedd4-2-/-) that develops IPF-like lung disease. The aim of this study was to characterize the onset and progression of IPF-like lung disease in conditional Nedd4-2-/- mice by longitudinal micro- computed tomography (CT). MethodsIn vivo micro-CT was performed longitudinally in control and conditional Nedd4- 2-/- mice at 1, 2, 3, 4 and 5 months after doxycycline induction. Further, terminal in vivo micro-CT followed by pulmonary function testing and post mortem micro-CT was performed in age-matched mice. Micro-CT images were evaluated for pulmonary fibrosis using an adapted fibrosis scoring system. ResultsMicro-CT is sensitive to detect onset and progression of pulmonary fibrosis in vivo and to quantify distinct radiological IPF-like features along disease development in conditional Nedd4-2-/- mice. Nonspecific interstitial alterations were detected from 3 months, whereas key features such as honeycombing-like lesions were detected from 4 months onwards. Pulmonary function inversely correlated with in vivo (r=-0.725) and post mortem (r=-0.535) micro-CT fibrosis scores. ConclusionLongitudinal micro-CT enables in vivo monitoring of onset and progression and detects radiologic key features of IPF-like lung disease in conditional Nedd4-2-/- mice. Our data support micro-CT as sensitive quantitative endpoint for preclinical evaluation of novel antifibrotic strategies. NEW & NOTEWORTHYIPF diagnosis, particularly in early stages, remains challenging. In this study micro-CT is used in conditional Nedd4-2-/- mice to closely monitor the onset and progression of IPF-like lung disease. This allowed us to track for the first time how nonspecific lung lesions develop into key IPF-like features. This approach offers a non-invasive method to monitor pulmonary fibrosis in vivo, providing a quantitative endpoint for preclinical evaluation of novel antifibrotic strategies.

pathology↗