Background: Modeling heterogeneous disease states by data-driven methods has great potential to advance biomedical research. However, a comprehensive analysis of phenotypic heterogeneity is often challenged by the complex nature of biomedical datasets and emerging imaging methodologies.
Methods: Here, we propose a novel GAN Inversion-enabled Latent Eigenvalue Analysis (GILEA) framework and apply it to in silico phenome profiling and editing.
Results: We show the performance of GILEA using cellular imaging datasets stained with the multiplexed fluorescence Cell Painting protocol. The quantitative results of GILEA can be biologically supported by editing of the latent representations and simulation of dynamic phenotype transitions between physiological and pathological states.
Conclusion: In conclusion, GILEA represents a new and broadly applicable approach to the quantitative and interpretable analysis of biomedical image data. The GILEA code and video demos are available at https://github.com/CTPLab/GILEA.
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http://dx.doi.org/10.1016/j.compbiomed.2024.108825 | DOI Listing |
Plants (Basel)
November 2024
Crop Research Institute, Guangdong Academy of Agriculture Sciences, Guangzhou 510640, China.
is a rare and precious medicinal and ornamental plant of Orchidaceae. Abundant morphological characteristics have been observed among cultivated accessions. Our understanding of the genetic basis of morphological diversity is limited due to a lack of sequence data and candidate genes.
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December 2024
Lee Kong Chian School of Medicine, Nanyang Technological University Singapore Singapore
The calcium-activated K3.1 channel plays a crucial role in T-cell immune response. Genetic manipulation of T-cells to upregulate the expression of K channels has been shown to boost T-cell cytotoxicity in cancer.
View Article and Find Full Text PDFExp Mol Pathol
December 2024
School of Medicine, National Tsing Hua University, Hsinchu 300044, Taiwan, ROC; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu 300044, Taiwan, ROC. Electronic address:
Diabetologia
January 2025
Unit of β Cell Biology, Diabetes Research Institute, IRCCS San Raffaele Hospital, Milan, Italy.
Aims/hypothesis: Wolfram syndrome 1 (WS1) is an inherited condition mainly manifesting in childhood-onset diabetes mellitus and progressive optic nerve atrophy. The causative gene, WFS1, encodes wolframin, a master regulator of several cellular responses, and the gene's mutations associate with clinical variability. Indeed, nonsense/frameshift variants correlate with more severe symptoms than missense/in-frame variants.
View Article and Find Full Text PDFReprod Sci
December 2024
School of Life Sciences, Human Phenome Institute, Fudan University, Shanghai, 200433, China.
Premature ovarian insufficiency (POI) is one of the leading causes of female infertility. To date, the genetic etiology of POI has been elucidated in approximately 20-25% of the total cases. The human zona pellucida (ZP) plays an important role in the organization and differentiation of granulosa cells, follicle formation, and sperm recognition.
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