KCRR: a nonlinear machine learning with a modified genomic similarity matrix improved the genomic prediction efficiency.

Nowadays, advances in high-throughput sequencing benefit the increasing application of genomic prediction (GP) in breeding programs. In this research, we designed a Cosine kernel-based KRR named KCRR to perform GP. This paper assessed the prediction accuracies of 12 traits with various heritability and genetic architectures from four populations using the genomic best linear unbiased prediction (GBLUP), BayesB, support vector regression (SVR), and KCRR. On the whole, KCRR performed stably for all traits of multiple species, indicating that the hypothesis of KCRR had the potential to be adapted to a wide range of genetic architectures. Moreover, we defined a modified genomic similarity matrix named Cosine similarity matrix (CS matrix). The results indicated that the accuracies between GBLUP_kinship and GBLUP_CS almost unanimously for all traits, but the computing efficiency has increased by an average of 20 times. Our research will be a significant promising strategy in future GP.

Cosine convolutional neural network and its application for seizure detection.

Traditional convolutional neural networks (CNNs) often suffer from high memory consumption and redundancy in their kernel representations, leading to overfitting problems and limiting their application in real-time, low-power scenarios such as seizure detection systems. In this work, a novel cosine convolutional neural network (CosCNN), which replaces traditional kernels with the robust cosine kernel modulated by only two learnable factors, is presented, and its effectiveness is validated on the tasks of seizure detection. Meanwhile, based on the cosine lookup table and KL-divergence, an effective post-training quantization algorithm is proposed for CosCNN hardware implementation. With quantization, CosCNN can achieve a nearly 75% reduction in the memory cost with almost no accuracy loss. Moreover, we design a configurable cosine convolution accelerator on Field Programmable Gate Array (FPGA) and deploy the quantized CosCNN on Zedboard, proving the proposed seizure detection system can operate in real-time and low-power scenarios. Extensive experiments and comparisons were conducted using two publicly available epileptic EEG databases, the Bonn database and the CHB-MIT database. The results highlight the performance superiority of the CosCNN over traditional CNNs as well as other seizure detection methods.

Incorporating kernelized multi-omics data improves the accuracy of genomic prediction.

BACKGROUND: Genomic selection (GS) has revolutionized animal and plant breeding after the first implementation via early selection before measuring phenotypes. Besides genome, transcriptome and metabolome information are increasingly considered new sources for GS. Difficulties in building the model with multi-omics data for GS and the limit of specimen availability have both delayed the progress of investigating multi-omics. RESULTS: We utilized the Cosine kernel to map genomic and transcriptomic data as [Formula: see text] symmetric matrix (G matrix and T matrix), combined with the best linear unbiased prediction (BLUP) for GS. Here, we defined five kernel-based prediction models: genomic BLUP (GBLUP), transcriptome-BLUP (TBLUP), multi-omics BLUP (MBLUP, [Formula: see text]), multi-omics single-step BLUP (mssBLUP), and weighted multi-omics single-step BLUP (wmssBLUP) to integrate transcribed individuals and genotyped resource population. The predictive accuracy evaluations in four traits of the Chinese Simmental beef cattle population showed that (1) MBLUP was far preferred to GBLUP (ratio = 1.0), (2) the prediction accuracy of wmssBLUP and mssBLUP had 4.18% and 3.37% average improvement over GBLUP, (3) We also found the accuracy of wmssBLUP increased with the growing proportion of transcribed cattle in the whole resource population. CONCLUSIONS: We concluded that the inclusion of transcriptome data in GS had the potential to improve accuracy. Moreover, wmssBLUP is accepted to be a promising alternative for the present situation in which plenty of individuals are genotyped when fewer are transcribed.