Craniofacial reconstruction in forensic science is crucial for the identification of the victims of crimes and disasters. The objective is to map a given skull to its corresponding face in a corpus of faces with known identities using recent advancements in computer vision, such as deep learning. In this paper, we presented a framework for the identification of a person given the X-ray image of a skull using convolutional Siamese networks for cross-domain identity representation. Siamese networks are twin networks that share the same architecture and can be trained to discover a feature space where nearby observations that are similar are grouped and dissimilar observations are moved apart. To do this, the network is exposed to two sets of comparable and different data. The Euclidean distance is then minimized between similar pairs and maximized between dissimilar ones. Since getting pairs of skull and face images are difficult, we prepared our own dataset of 40 volunteers whose front and side skull X-ray images and optical face images were collected. Experiments were conducted on the collected cross-domain dataset to train and validate the Siamese networks. The experimental results provide satisfactory results on the identification of a person from the given skull.

Current challenges in developing foundational models for volumetric imaging data, such as magnetic resonance imaging (MRI), stem from the computational complexity of training state-of-the-art architectures in high dimensions and curating sufficiently large datasets of volumes. To address these challenges, we introduce Raptor (Random Planar Tensor Reduction), a train-free method for generating semantically rich embeddings for volumetric data. Raptor leverages a frozen 2D foundation model, pretrained on natural images, to extract visual tokens from individual cross-sections of medical volumes. These tokens are then spatially compressed using random projections, significantly reducing computational complexity while retaining semantic information. Extensive experiments on ten diverse medical volume tasks verify the superior performance of Raptor over state-of-the-art methods, including those pretrained exclusively on medical volumes (+3% SuPreM, +6% MISFM, +10% Merlin, +13% VoCo, and +14% SLIViT), while entirely bypassing the need for costly training. Our results highlight the effectiveness and versatility of Raptor as a foundation for advancing deep learning-based methods for medical volumes.

Deep learning has driven significant advances in medical image analysis, yet its adoption in clinical practice remains constrained by the large size and lack of transparency in modern models. Advances in interpretability techniques such as DL-Backtrace, Layer-wise Relevance Propagation, and Integrated Gradients make it possible to assess the contribution of individual components within neural networks trained on medical imaging tasks. In this work, we introduce an interpretability-guided pruning framework that reduces model complexity while preserving both predictive performance and transparency. By selectively retaining only the most relevant parts of each layer, our method enables targeted compression that maintains clinically meaningful representations. Experiments across multiple medical image classification benchmarks demonstrate that this approach achieves high compression rates with minimal loss in accuracy, paving the way for lightweight, interpretable models suited for real-world deployment in healthcare settings.

Medical image retrieval is a valuable field for supporting clinical decision-making, yet current methods primarily support 2D images and require fully annotated queries, limiting clinical flexibility. To address this, we propose RadiomicsRetrieval, a 3D content-based retrieval framework bridging handcrafted radiomics descriptors with deep learning-based embeddings at the tumor level. Unlike existing 2D approaches, RadiomicsRetrieval fully exploits volumetric data to leverage richer spatial context in medical images. We employ a promptable segmentation model (e.g., SAM) to derive tumor-specific image embeddings, which are aligned with radiomics features extracted from the same tumor via contrastive learning. These representations are further enriched by anatomical positional embedding (APE). As a result, RadiomicsRetrieval enables flexible querying based on shape, location, or partial feature sets. Extensive experiments on both lung CT and brain MRI public datasets demonstrate that radiomics features significantly enhance retrieval specificity, while APE provides global anatomical context essential for location-based searches. Notably, our framework requires only minimal user prompts (e.g., a single point), minimizing segmentation overhead and supporting diverse clinical scenarios. The capability to query using either image embeddings or selected radiomics attributes highlights its adaptability, potentially benefiting diagnosis, treatment planning, and research on large-scale medical imaging repositories. Our code is available at https://github.com/nainye/RadiomicsRetrieval.

Solving computer vision problems through machine learning, one often encounters lack of sufficient training data. To mitigate this we propose the use of ensembles of weak learners based on spectral total-variation (STV) features (Gilboa 2014). The features are related to nonlinear eigenfunctions of the total-variation subgradient and can characterize well textures at various scales. It was shown (Burger et-al 2016) that, in the one-dimensional case, orthogonal features are generated, whereas in two-dimensions the features are empirically lowly correlated. Ensemble learning theory advocates the use of lowly correlated weak learners. We thus propose here to design ensembles using learners based on STV features. To show the effectiveness of this paradigm we examine a hard real-world medical imaging problem: the predictive value of computed tomography (CT) data for high uptake in positron emission tomography (PET) for patients suspected of skeletal metastases. The database consists of 457 scans with 1524 unique pairs of registered CT and PET slices. Our approach is compared to deep-learning methods and to Radiomics features, showing STV learners perform best (AUC=0.87), compared to neural nets (AUC=0.75) and Radiomics (AUC=0.79). We observe that fine STV scales in CT images are especially indicative for the presence of high uptake in PET.

Predicting distant metastases in soft tissue sarcomas (STS) is vital for guiding clinical decision-making. Recent advancements in radiomics and deep learning (DL) models have shown promise, but their diagnostic accuracy remains unclear. This meta-analysis aims to assess the performance of radiomics and DL-based models in predicting metastases in STS by analyzing pooled sensitivity and specificity. Following PRISMA guidelines, a thorough search was conducted in PubMed, Web of Science, and Embase. A random-effects model was used to estimate the pooled area under the curve (AUC), sensitivity, and specificity. Subgroup analyses were performed based on imaging modality (MRI, PET, PET/CT), feature extraction method (DL radiomics [DLR] vs. handcrafted radiomics [HCR]), incorporation of clinical features, and dataset used. Heterogeneity by I² statistic, leave-one-out sensitivity analyses, and publication bias by Egger's test assessed model robustness and potential biases. Ninetheen studies involving 1712 patients were included. The pooled AUC for predicting metastasis was 0.88 (95% CI: 0.80-0.92). The pooled AUC values were 88% (95% CI: 77-89%) for MRI-based models, 80% (95% CI: 76-92%) for PET-based models, and 91% (95% CI: 78-93%) for PET/CT-based models, with no significant differences (p = 0.75). DL-based models showed significantly higher sensitivity than HCR models (p < 0.01). Including clinical features did not significantly improve model performance (AUC: 0.90 vs. 0.88, p = 0.99). Significant heterogeneity was noted (I² > 25%), and Egger's test suggested potential publication bias (p < 0.001). Radiomics models showed promising potential for predicting metastases in STSs, with DL approaches outperforming traditional HCR. While integrating this approach into routine clinical practice is still evolving, it can aid physicians in identifying high-risk patients and implementing targeted monitoring strategies to reduce the risk of severe complications associated with metastasis. However, challenges such as heterogeneity, limited external validation, and potential publication bias persist. Future research should concentrate on standardizing imaging protocols and conducting multi-center validation studies to improve the clinical applicability of radiomics predictive models.

Pneumonia detection in chest X-rays (CXR) increasingly relies on AI-driven diagnostic systems. However, their "black-box" nature often lacks transparency, underscoring the need for interpretability to improve patient outcomes. This study presents the first application of the Deformable Prototypical Part Network (D-ProtoPNet), an ante-hoc interpretable deep learning (DL) model, for pneumonia classification in pediatric patients' CXR images. Clinical insights were integrated through expert radiologist evaluation of the model's learned prototypes and activated image patches, ensuring that explanations aligned with medically meaningful features. The model was developed and tested on a retrospective dataset of 5,856 CXR images of pediatric patients, ages 1-5 years. The images were originally acquired at a tertiary academic medical center as part of routine clinical care and were publicly hosted on a Kaggle platform. This dataset comprised anterior-posterior images labeled normal, viral, and bacterial. It was divided into 80 % training and 20 % validation splits, and utilised in a supervised five-fold cross-validation. Performance metrics were compared with the original ProtoPNet, utilising ResNet50 as the base model. An experienced radiologist assessed the clinical relevance of the learned prototypes, patch activations, and model explanations. The D-ProtoPNet achieved an accuracy of 86 %, precision of 86 %, recall of 85 %, and AUC of 93 %, marking a 3 % improvement over the original ProtoPNet. While further optimisation is required before clinical use, the radiologist praised D-ProtoPNet's intuitive explanations, highlighting its interpretability and potential to aid clinical decision-making. Prototypical part learning offers a balance between classification performance and explanation quality, but requires improvements to match the accuracy of black-box models. This study underscores the importance of integrating domain expertise during model evaluation to ensure the interpretability of XAI models is grounded in clinically valid insights.

Lung cancer remains the leading cause of cancer-related mortality worldwide, largely due to late-stage diagnosis. Early detection is critical for improving patient outcomes, yet current screening methods, such as low-dose computed tomography (CT), often lack the sensitivity and specificity required for early-stage detection. Here, we present a multimodal early screening platform that integrates a multiplexed laser-induced graphene (LIG) immunosensor with machine learning to enhance the accuracy of lung cancer diagnosis. Our platform enables the rapid, cost-effective, and simultaneous detection of four tumor markers─neuron-specific enolase (NSE), carcinoembryonic antigen (CEA), p53, and SOX2─with limits of detection (LOD) as low as 1.62 pg/mL. By combining proteomic data from the immunosensor with deep learning-based CT imaging features and clinical data, we developed a multimodal predictive model that achieves an area under the curve (AUC) of 0.936, significantly outperforming single-modality approaches. This platform offers a transformative solution for early lung cancer screening, particularly in resource-limited settings, and provides potential technical support for precision medicine in oncology.

Medical imaging sciences and diagnostic techniques for Breast Cancer (BC) imaging have advanced tremendously, particularly with the use of mammography images; however, radiologists may still misinterpret medical images of the breast, resulting in limitations and flaws in the screening process. As a result, Computer-Aided Design (CAD) systems have become increasingly popular due to their ability to operate independently of human analysis. Current CAD systems use grayscale analysis, which lacks the contrast needed to differentiate benign from malignant lesions. As part of this study, an innovative CAD system is presented that transforms standard grayscale mammography images into RGB colored through a three-path preprocessing framework developed for noise reduction, lesion highlighting, and tumor-centric intensity adjustment using a data-driven transfer function. In contrast to a generic approach, this approach statistically tailors colorization in order to emphasize malignant regions, thus enhancing the ability of both machines and humans to recognize cancerous areas. As a consequence of this conversion, breast tumors with anomalies become more visible, which allows us to extract more accurate features about them. In a subsequent step, Machine Learning (ML) algorithms are employed to classify these tumors as malign or benign cases. A pre-trained model is developed to extract comprehensive features from colored mammography images by employing this approach. A variety of techniques are implemented in the pre-processing section to minimize noise and improve image perception; however, the most challenging methodology is the application of creative techniques to adjust pixels' intensity values in mammography images using a data-driven transfer function derived from tumor intensity histograms. This adjustment serves to draw attention to tumors while reducing the brightness of other areas in the breast image. Measuring criteria such as accuracy, sensitivity, specificity, precision, F1-Score, and Area Under the Curve (AUC) are used to evaluate the efficacy of the employed methodologies. This work employed and tested a variety of pre-training and ML techniques. However, the combination of EfficientNetB0 pre-training with ML Support Vector Machines (SVM) produced optimal results with accuracy, sensitivity, specificity, precision, F1-Score, and AUC, of 99.4%, 98.7%, 99.1%, 99%, 98.8%, and 100%, respectively. It is clear from these results that the developed method does not only advance the state-of-the-art in technical terms, but also provides radiologists with a practical tool to aid in the reduction of diagnostic errors and increase the detection of early breast cancer.

Develop a fusion model based on explainable machine learning, combining multiparametric MRI subregional radiomics and deep learning, to preoperatively predict the lymphovascular invasion status in rectal cancer. We collected data from RC patients with histopathological confirmation from two medical centers, with 301 patients used as a training set and 75 patients as an external validation set. Using K-means clustering techniques, we meticulously divided the tumor areas into multiple subregions and extracted crucial radiomic features from them. Additionally, we employed an advanced Vision Transformer (ViT) deep learning model to extract features. These features were integrated to construct the SubViT model. To better understand the decision-making process of the model, we used the Shapley Additive Properties (SHAP) tool to evaluate the model's interpretability. Finally, we comprehensively assessed the performance of the SubViT model through receiver operating characteristic (ROC) curves, decision curve analysis (DCA), and the Delong test, comparing it with other models. In this study, the SubViT model demonstrated outstanding predictive performance in the training set, achieving an area under the curve (AUC) of 0.934 (95% confidence interval: 0.9074 to 0.9603). It also performed well in the external validation set, with an AUC of 0.884 (95% confidence interval: 0.8055 to 0.9616), outperforming both subregion radiomics and imaging-based models. Furthermore, decision curve analysis (DCA) indicated that the SubViT model provides higher clinical utility compared to other models. As an advanced composite model, the SubViT model demonstrated its efficiency in the non-invasive assessment of local vascular invasion (LVI) in rectal cancer.