TY - JOUR A1 - Mohammadzadeh, Saeed A1 - H. Nascimento, Vítor A1 - C. de Lamare, Rodrigo A1 - Hajarolasvadi, Noushin T1 - Robust Beamforming Based on Complex-Valued Convolutional Neural Networks for Sensor Arrays JF - IEEE Signal Processing Letters N2 - Robust adaptive beamforming (RAB) plays a vital role in modern communications by ensuring the reception of high-quality signals. This article proposes a deep learning approach to robust adaptive beamforming. In particular, we propose a novel RAB approach where the sample covariance matrix (SCM) is used as the input of a deep 1D Complex-Valued Convolutional Neural Network (CVCNN). The network employs complex convolutional and pooling layers, as well as a Cartesian Scaled Exponential Linear Unit activation function to directly compute the nearly-optimum weight vector through the training process and without prior knowledge about the direction of arrival of the desired signal. This means that reconstruction of the interference plus noise (IPN) covariance matrix is not required. The trained CVCNN accurately computes the nearly-optimum weight vector for data not used during training. The computed weight vector is employed to estimate the signal-to-interference plus noise ratio. Simulations show that the proposed RAB can provide performance close to that of the optimal beamformer. Y1 - 2022 U6 - https://doi.org/10.1109/LSP.2022.3212637 VL - 29 SP - 2018 EP - 2021 ER - TY - JOUR A1 - Hajarolasvadi, Noushin A1 - Sunkara, Vikram A1 - Khavnekar, Sagar A1 - Beck, Florian A1 - Brandt, Robert A1 - Baum, Daniel T1 - Volumetric macromolecule identification in cryo-electron tomograms using capsule networks JF - BMC Bioinformatics N2 - Background: Despite recent advances in cellular cryo-electron tomography (CET), developing automated tools for macromolecule identification in submolecular resolution remains challenging due to the lack of annotated data and high structural complexities. To date, the extent of the deep learning methods constructed for this problem is limited to conventional Convolutional Neural Networks (CNNs). Identifying macromolecules of different types and sizes is a tedious and time-consuming task. In this paper, we employ a capsule-based architecture to automate the task of macro- molecule identification, that we refer to as 3D-UCaps. In particular, the architecture is composed of three components: feature extractor, capsule encoder, and CNN decoder. The feature extractor converts voxel intensities of input sub-tomograms to activities of local features. The encoder is a 3D Capsule Network (CapsNet) that takes local features to generate a low-dimensional representation of the input. Then, a 3D CNN decoder reconstructs the sub-tomograms from the given representation by upsampling. Results: We performed binary and multi-class localization and identification tasks on synthetic and experimental data. We observed that the 3D-UNet and the 3D-UCaps had an F1−score mostly above 60% and 70%, respectively, on the test data. In both network architectures, we observed degradation of at least 40% in the F1-score when identifying very small particles (PDB entry 3GL1) compared to a large particle (PDB entry 4D8Q). In the multi-class identification task of experimental data, 3D-UCaps had an F1-score of 91% on the test data in contrast to 64% of the 3D-UNet. The better F1-score of 3D-UCaps compared to 3D-UNet is obtained by a higher precision score. We speculate this to be due to the capsule network employed in the encoder. To study the effect of the CapsNet-based encoder architecture further, we performed an ablation study and perceived that the F1-score is boosted as network depth is increased which is in contrast to the previously reported results for the 3D-UNet. To present a reproducible work, source code, trained models, data as well as visualization results are made publicly available. Conclusion: Quantitative and qualitative results show that 3D-UCaps successfully perform various downstream tasks including identification and localization of macro- molecules and can at least compete with CNN architectures for this task. Given that the capsule layers extract both the existence probability and the orientation of the molecules, this architecture has the potential to lead to representations of the data that are better interpretable than those of 3D-UNet. Y1 - 2022 U6 - https://doi.org/10.1186/s12859-022-04901-w VL - 23 IS - 360 ER - TY - GEN A1 - Hajarolasvadi, Noushin A1 - Baum, Daniel T1 - Data for Training the DeepOrientation Model: Simulated cryo-ET tomogram patches N2 - A major restriction to applying deep learning methods in cryo-electron tomography is the lack of annotated data. Many large learning-based models cannot be applied to these images due to the lack of adequate experimental ground truth. One appealing alternative solution to the time-consuming and expensive experimental data acquisition and annotation is the generation of simulated cryo-ET images. In this context, we exploit a public cryo-ET simulator called PolNet to generate three datasets of two macromolecular structures, namely the ribosomal complex 4v4r and Thermoplasma acidophilum 20S proteasome, 3j9i. We select these two specific particles to test whether our models work for macromolecular structures with and without rotational symmetry. The three datasets contain 50, 150, and 450 tomograms with a voxel size of 10 ̊A, respectively. Here, we publish patches of size 40 × 40 × 40 extracted from the medium-sized dataset with 26,703 samples of 4v4r and 40,671 samples of 3j9i. The original tomograms from which the samples were extracted are of size 500 × 500 × 250. Finally, it should be noted that the currently published test dataset is employed for reporting the results of our paper titled ”DeepOrientation: Deep Orientation Estimation of Macromolecules in Cryo-electron tomography” paper. Y1 - 2024 U6 - https://doi.org/10.12752/9686 ER -