Feature-Based Occupancy Map-Merging for Collaborative SLAM.

One of the most frequently used approaches to represent collaborative mapping are probabilistic occupancy grid maps. These maps can be exchanged and integrated among robots to reduce the overall exploration time, which is the main advantage of the collaborative systems. Such map fusion requires solving the unknown initial correspondence problem. This article presents an effective feature-based map fusion approach that includes processing the spatial occupancy probabilities and detecting features based on locally adaptive nonlinear diffusion filtering. We also present a procedure to verify and accept the correct transformation to avoid ambiguous map merging. Further, a global grid fusion strategy based on the Bayesian inference, which is independent of the order of merging, is also provided. It is shown that the presented method is suitable for identifying geometrically consistent features across various mapping conditions, such as low overlapping and different grid resolutions. We also present the results based on hierarchical map fusion to merge six individual maps at once in order to constrict a consistent global map for SLAM.

Multi-omics Data Integration Model Based on UMAP Embedding and Convolutional Neural Network.

Introduction: Multi-omics data integration facilitates collecting richer understanding and perceptions than separate omics data. Various promising integrative approaches have been utilized to analyze multi-omics data for biomedical applications, including disease prediction and disease subtypes, biomarker prediction, and others. Methods: In this paper, we introduce a multi-omics data integration method that is constructed using the combination of gene similarity network (GSN) based on uniform manifold approximation and projection (UMAP) and convolutional neural networks (CNNs). The method utilizes UMAP to embed gene expression, DNA methylation, and copy number alteration (CNA) to a lower dimension creating two-dimensional RGB images. Gene expression is used as a reference to construct the GSN and then integrate other omics data with the gene expression for better prediction. We used CNNs to predict the Gleason score levels of prostate cancer patients and the tumor stage in breast cancer patients. Results: The model proposed near perfection with accuracy above 99% with all other performance measurements at the same level. The proposed model outperformed the state-of-art iSOM-GSN model that constructs the GSN map based on the self-organizing map. Conclusion: The results show that UMAP as an embedding technique can better integrate multi-omics maps into the prediction model than SOM. The proposed model can also be applied to build a multi-omics prediction model for other types of cancer.

Machine learning-based prediction of upgrading on magnetic resonance imaging targeted biopsy in patients eligible for active surveillance.

OBJECTIVE: To examine the ability of machine learning methods to predict upgrading of Gleason score on confirmatory magnetic resonance imaging-guided targeted biopsy (MRI-TB) of the prostate in candidates for active surveillance. SUBJECTS AND METHODS: Our database included 592 patients who received prostate multiparametric magnetic resonance imaging in the evaluation for active surveillance. Upgrading to significant prostate cancer on MRI-TB was defined as upgrading to G 3+4 (definition 1 - DF1) and 4+3 (DF2). Machine learning classifiers were applied on both classification problems DF1 and DF2. RESULTS: Univariate analysis showed that older age and the number of positive cores on pre-MRI-TB were positively correlated with upgrading by DF1 (P-value ≤ 0.05). Upgrading by DF2 was positively correlated with age and the number of positive cores and negatively correlated with body mass index. For upgrading prediction, the AdaBoost model was highly predictive of upgrading by DF1 (AUC 0.952), while for prediction of upgrading by DF2, the Random Forest model had a lower but excellent prediction performance (AUC 0.947). CONCLUSION: We show that machine learning has the potential to be integrated in future diagnostic assessments for patients eligible for AS. Training our models on larger multi-institutional databases is needed to confirm our results and improve the accuracy of these models' prediction.