Utilizing the Double-Precision Floating-Point Computing Power of GPUs for RSA Acceleration

Asymmetric cryptographic algorithm (e.g., RSA and Elliptic Curve Cryptography) implementations on Graphics Processing Units (GPUs) have been researched for over a decade. The basic idea of most previous contributions is exploiting the highly parallel GPU architecture and porting the integer-based algorithms from general-purpose CPUs to GPUs, to offer high performance. However, the great potential cryptographic computing power of GPUs, especially by the more powerful floating-point instructions, has not been comprehensively investigated in fact. In this paper, we fully exploit the floating-point computing power of GPUs, by various designs, including the floating-point-based Montgomery multiplication/exponentiation algorithm and Chinese Remainder Theorem (CRT) implementation in GPU. And for practical usage of the proposed algorithm, a new method is performed to convert the input/output between octet strings and floating-point numbers, fully utilizing GPUs and further promoting the overall performance by about 5%. The performance of RSA-2048/3072/4096 decryption on NVIDIA GeForce GTX TITAN reaches 42,211/12,151/5,790 operations per second, respectively, which achieves 13 times the performance of the previous fastest floating-point-based implementation (published in Eurocrypt 2009). The RSA-4096 decryption precedes the existing fastest integer-based result by 23%

ConvKyber: Unleashing the Power of AI Accelerators for Faster Kyber with Novel Iteration-based Approaches

The remarkable performance capabilities of AI accelerators offer promising opportunities for accelerating cryptographic algorithms, particularly in the context of lattice-based cryptography. However, current approaches to leveraging AI accelerators often remain at a rudimentary level of implementation, overlooking the intricate internal mechanisms of these devices. Consequently, a significant number of computational resources is underutilized. In this paper, we present a comprehensive exploration of NVIDIA Tensor Cores and introduce a novel framework tailored specifically for Kyber. Firstly, we propose two innovative approaches that efficiently break down Kyber\u27s NTT into iterative matrix multiplications, resulting in approximately a 75% reduction in costs compared to the state-of-the-art scanning-based methods.Secondly, by reversing the internal mechanisms, we precisely manipulate the internal resources of Tensor Cores using assembly-level code instead of inefficient standard interfaces, eliminating memory accesses and redundant function calls. Finally, building upon our highly optimized NTT, we provide a complete implementation for all parameter sets of Kyber. Our implementation surpasses the state-of-the-art Tensor Core based work, achieving remarkable speed-ups of 1.93x, 1.65x, 1.22x and 3.55x for polyvec_ntt, KeyGen, Enc and Dec in Kyber-1024, respectively. Even when considering execution latency, our throughput-oriented full Kyber implementation maintains an acceptable execution latency. For instance, the execution latency ranges from 1.02 to 5.68 milliseconds for Kyber-1024 on R3080 when achieving the peak throughput

ConvKyber: Unleashing the Power of AI Accelerators for Faster Kyber with Novel Iteration-based Approaches

The remarkable performance capabilities of AI accelerators offer promising opportunities for accelerating cryptographic algorithms, particularly in the context of lattice-based cryptography. However, current approaches to leveraging AI accelerators often remain at a rudimentary level of implementation, overlooking the intricate internal mechanisms of these devices. Consequently, a significant number of computational resources is underutilized. In this paper, we present a comprehensive exploration of NVIDIA Tensor Cores and introduce a novel framework tailored specifically for Kyber. Firstly, we propose two innovative approaches that efficiently break down Kyber’s NTT into iterative matrix multiplications, resulting in approximately a 75% reduction in costs compared to the state-of-the-art scanning-based methods. Secondly, by reversing the internal mechanisms, we precisely manipulate the internal resources of Tensor Cores using assembly-level code instead of inefficient standard interfaces, eliminating memory accesses and redundant function calls. Finally, building upon our highly optimized NTT, we provide a complete implementation for all parameter sets of Kyber. Our implementation surpasses the state-of-the-art Tensor Core based work, achieving remarkable speed-ups of 1.93x, 1.65x, 1.22x and 3.55x for polyvec_ntt, KeyGen, Enc and Dec in Kyber-1024, respectively. Even when considering execution latency, our throughput-oriented full Kyber implementation maintains an acceptable execution latency. For instance, the execution latency ranges from 1.02 to 5.68 milliseconds for Kyber-1024 on R3080 when achieving the peak throughput

A Novel High-performance Implementation of CRYSTALS-Kyber with AI Accelerator

Public-key cryptography, including conventional cryptosystems and post-quantum cryptography, involves computation-intensive workloads. With noticing the extraordinary computing power of AI accelerators, in this paper, we further explore the feasibility to introduce AI accelerators into high-performance cryptographic computing. Since AI accelerators are dedicated to machine learning or neural networks, the biggest challenge is how to transform cryptographic workloads into their operations, while ensuring the correctness of the results and bringing convincing performance gains. After investigating and analysing the workload of NVIDIA AI accelerator, Tensor Core, we choose to utilize it to accelerate the polynomial multiplication, usually the most time-consuming part in lattice-based cryptography. We take measures to accommodate the matrix-multiply-and-add mode of Tensor Core and make a trade-off between precision and performance, to leverage it as a high-performance NTT box performing NTT/INTT through CUDA C++ WMMA APIs. Meanwhile, we take CRYSTALS-Kyber, the candidate to be standardized by NIST, as a case study on RTX 3080 with the Ampere Tensor Core. The empirical results show that the customized NTT of polynomial vector ($n=256,k=4$) with our NTT box obtains a speedup around 6.47x that of the state-of-the-art implementation on the same GPU platform. Compared with the AVX2 implementation submitted to NIST, our Kyber-1024 can achieve a speedup of 26x, 36x, and 35x for each phase

The Genomes of Oryza sativa: A History of Duplications

We report improved whole-genome shotgun sequences for the genomes of indica and japonica rice, both with multimegabase contiguity, or almost 1,000-fold improvement over the drafts of 2002. Tested against a nonredundant collection of 19,079 full-length cDNAs, 97.7% of the genes are aligned, without fragmentation, to the mapped super-scaffolds of one or the other genome. We introduce a gene identification procedure for plants that does not rely on similarity to known genes to remove erroneous predictions resulting from transposable elements. Using the available EST data to adjust for residual errors in the predictions, the estimated gene count is at least 38,000–40,000. Only 2%–3% of the genes are unique to any one subspecies, comparable to the amount of sequence that might still be missing. Despite this lack of variation in gene content, there is enormous variation in the intergenic regions. At least a quarter of the two sequences could not be aligned, and where they could be aligned, single nucleotide polymorphism (SNP) rates varied from as little as 3.0 SNP/kb in the coding regions to 27.6 SNP/kb in the transposable elements. A more inclusive new approach for analyzing duplication history is introduced here. It reveals an ancient whole-genome duplication, a recent segmental duplication on Chromosomes 11 and 12, and massive ongoing individual gene duplications. We find 18 distinct pairs of duplicated segments that cover 65.7% of the genome; 17 of these pairs date back to a common time before the divergence of the grasses. More important, ongoing individual gene duplications provide a never-ending source of raw material for gene genesis and are major contributors to the differences between members of the grass family

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

On-deck vs. laboratory analyses of the sound velocity of sediments from the Huanghai and Bohai seas

One popular method of obtaining the acoustic parameters of seabed sediments is by measuring the sound velocity of sediment samples in a laboratory. However, the effects of environmental variation and physical perturbation on acoustic properties are typically neglected in the application of such measured acoustic parameters. In this study, sediment samples were collected from the Huanghai and Bohai seas to measure sound velocity both on the deck and in the laboratory using a digital sonic measuring system. Additionally, sediment compositions, physical and mechanical properties and microstructures were determined. Sound velocity comparisons between on-deck and laboratory measurements indicate that laboratory-measured velocities are generally higher than those measured on the deck, with differences ranging from 1.45 m/s to 130.05 m/s, due to the water loss and densification of sedimentary particles in laboratory settings. The discrepancy of sound velocities measured in the laboratory and on the deck also differ based on the types of sediments sampled. Overall, the discrepancy increases with measurement frequency, increasing average grain diameter and sand content, as well as with decreasing clay content

Transmission Electron Microscopy Studies of Cellular Responses to Entry of Virions: One Kind of Natural Nanobiomaterial

Virions are one kind of nanoscale pathogen and are able to infect living cells of animals, plants, and bacteria. The infection is an intrinsic property of the virions, and the biological process provides a good model for studying how these nanoparticles enter into cells. During the infection, the viruses employ different strategies to which the cells have developed respective responses. For this paper, we chose Bombyx mori cypovirus 1 (BmCPV-1) interactions with midgut cells from silkworm, and severe acute respiratory syndrome (SARS) associated coronavirus interactions with Vero E6 cells, as examples to demonstrate the response of eukaryotic cells to two different types of virus from our previous studies. The bacteriophage-bacteria interactions are also introduced to elucidate how the bacteriophage conquers the barrier of cell walls in the prokaryotic cells to transport genome into the host

Structure determination of a human virus by the combination of cryo-EM and X-ray crystallography

Virus 3D atomic structures provide insight into our understanding of viral life cycles and the development of antiviral drugs. X-ray crystallography and cryo-EM have been used to determine the atomic structure of viruses. However, limited availability of biological samples, biosafety issues due to virus infection, and sometimes inherent characteristics of viruses, pose difficulties on combining both methods in determining viral structures. These have made solving the high resolution structure of some medically important viruses very challenging. Here, we describe our recently employed protocols for determining the high-resolution structure of the virus-like particle of hepatitis E virus (HEV), a pathogen of viral hepatitis in human. These protocols include utilizing recombinant baculovirus system to generate sufficient amount of virus particles, single-particle cryo-EM to get an intermediate resolution structure as a phasing model, and X-ray crystallography for final atomic structure determination. Our protocols have solved the hepatitis E virus structure to the resolution of 3.5 Å. The combined methodology is generally applicable to other human infectious viruses