Cryo-electron microscopy (cryo-EM) is a key technique for structural biology, but its computational efficiency, particularly during 3D reconstruction, remains a bottleneck. We introduce T2-RELION, a highly optimized version of RELION for cryo-EM 3D reconstruction on CPU-GPU platforms. RELION is a widely used open-source package in the cryo-EM community. We identify and resolve key inefficiencies in RELION’s parallelization strategy and memory management by proposing task parallelism and a three-phase GPU memory management strategy. Furthermore, we leverage Tensor Cores to accelerate the hot-spot kernel for difference calculation, employing an advanced pipelining strategy to hide latency and enable thread-block-level data reuse. On a quad-A100 GPU machine, performance evaluations demonstrate that T2-RELION outperforms RELION 4.0. For the hot-spot kernel, our optimizations achieve 1.90-23.7 times speedup. For the whole application using CNG and Trpv1 datasets, we observe 3.86 times and 2.68 times speedups, respectively.

The fast development of biomolecular structure determination has enabled the fine-grained study of objects in the micro-world, such as proteins and RNAs. The world is benefited. However, as the computational algorithms are constantly developed, the enrichment of features increases the algorithmic complexity and brings more computationally unfriendly modules. It calls for efficient solutions to leverage the rich and various hardware resources from the world’s most state-of-the-art supercomputing systems, and to fully accelerate the performance of the applications. In this article, we present our efforts on porting and optimizing the 3D reconstruction of RELION, one of the most popular cryo-EM software for biomolecular structure determinations, by leveraging different resources of the latest generation of Sunway heterogeneous supercomputer. Several novel approaches are proposed to resolve different challenges faced by the complex algorithm, including a multi-level parallel scheme and operator optimizations to smartly map and scale RELION, efficient strategies to largely address the memory bottlenecks and improve data locality, lock-free writing solutions to minimize write-write conflicts, and pipelining approaches to obtain excellent computation and communication overlap. Combining all proposed optimizations, the computation time is greatly reduced to under 2 hours, achieving 11.9× and 8.9× speedups on two different datasets. The overall design scales to 131,072 cores, increasing parallel efficiency from 33% to 61% and from 46% to 70%, respectively. To the best of our knowledge, this is the first work that fully optimized and scaled the 3D reconstruction of RELION using the latest Sunway system.

SUMMARY: Structural visualization and analysis are fundamental to explore macromolecular functions. Here, we present a novel integrative web-based virtual reality (VR) system-VRmol, to visualize and study molecular structures in an immersive virtual environment. Importantly, it is integrated with multiple online databases and is able to couple structure studies with associated genomic variations and drug information in a visual interface by cloud-based drug docking. VRmol thus can serve as an integrative platform to aid structure-based translational research and drug design. AVAILABILITY AND IMPLEMENTATION: VRmol is freely available (https://VRmol.net), with detailed manual and tutorial (https://VRmol.net/docs). The code of VRmol is available as open source under the MIT license at http://github.com/kuixu/VRmol. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.