PaLM 2 Technical Report

We introduce PaLM 2, a new state-of-the-art language model that has better multilingual and reasoning capabilities and is more compute-efficient than its predecessor PaLM. PaLM 2 is a Transformer-based model trained using a mixture of objectives. Through extensive evaluations on English and multilingual language, and reasoning tasks, we demonstrate that PaLM 2 has significantly improved quality on downstream tasks across different model sizes, while simultaneously exhibiting faster and more efficient inference compared to PaLM. This improved efficiency enables broader deployment while also allowing the model to respond faster, for a more natural pace of interaction. PaLM 2 demonstrates robust reasoning capabilities exemplified by large improvements over PaLM on BIG-Bench and other reasoning tasks. PaLM 2 exhibits stable performance on a suite of responsible AI evaluations, and enables inference-time control over toxicity without additional overhead or impact on other capabilities. Overall, PaLM 2 achieves state-of-the-art performance across a diverse set of tasks and capabilities. When discussing the PaLM 2 family, it is important to distinguish between pre-trained models (of various sizes), fine-tuned variants of these models, and the user-facing products that use these models. In particular, user-facing products typically include additional pre- and post-processing steps. Additionally, the underlying models may evolve over time. Therefore, one should not expect the performance of user-facing products to exactly match the results reported in this report

A Nonlinear Blind Source Separation Method Based On Radial Basis Function and Quantum Genetic Algorithm

Blind source separation is a hot topic in signal processing. Most existing works focus on dealing with linear combined signals, while in practice we always encounter with nonlinear mixed signals. To address the problem of nonlinear source separation, in this paper we propose a novel algorithm using radial basis function neutral network, optimized by multi-universe parallel quantum genetic algorithm. Experiments show the efficiency of the proposed method

A Nonlinear Blind Source Separation Method Based On Radial Basis Function and Quantum Genetic Algorithm

Blind source separation is a hot topic in signal processing. Most existing works focus on dealing with linear combined signals, while in practice we always encounter with nonlinear mixed signals. To address the problem of nonlinear source separation, in this paper we propose a novel algorithm using radial basis function neutral network, optimized by multi-universe parallel quantum genetic algorithm. Experiments show the efficiency of the proposed method

High Dimensional Electromagnetic Interference Signal Clustering Based On SOM Neural Network

In this paper, we study the spectral characteristics and global representations of strongly nonlinear, non-stationary electromagnetic interferences (EMI), which is of great significance in analysing the mathematical modelling of electromagnetic capability (EMC) for a large scale integrated system. We firstly propose to use Self-Organizing Feature Map Neural Network (SOM) to cluster EMI signals. To tackle with the high dimensionality of EMI signals, we combine the dimension reduction and clustering approaches, and find out the global features of different interference factors, in order to finally provide precise mathematical simulation models for EMC design, analysis, forecasting and evaluation. Experimental results have demonstrated the validity and effectiveness of the proposed method

TCMSP: a database of systems pharmacology for drug discovery from herbal medicines

Background: Modern medicine often clashes with traditional medicine such as Chinese herbal medicine because of the little understanding of the underlying mechanisms of action of the herbs. In an effort to promote integration of both sides and to accelerate the drug discovery from herbal medicines, an efficient systems pharmacology platform that represents ideal information convergence of pharmacochemistry, ADME properties, drug-likeness, drug targets, associated diseases and interaction networks, are urgently needed

Insights from systems pharmacology into cardiovascular drug discovery and therapy

Background: Given the complex nature of cardiovascular disease (CVD), information derived from a systems-level will allow us to fully interrogate features of CVD to better understand disease pathogenesis and to identify new drug targets

Single-cell RNA-seq analysis of mouse preimplantation embryos by third-generation sequencing.

The development of next generation sequencing (NGS) platform-based single-cell RNA sequencing (scRNA-seq) techniques has tremendously changed biological researches, while there are still many questions that cannot be addressed by them due to their short read lengths. We developed a novel scRNA-seq technology based on third-generation sequencing (TGS) platform (single-cell amplification and sequencing of full-length RNAs by Nanopore platform, SCAN-seq). SCAN-seq exhibited high sensitivity and accuracy comparable to NGS platform-based scRNA-seq methods. Moreover, we captured thousands of unannotated transcripts of diverse types, with high verification rate by reverse transcription PCR (RT-PCR)-coupled Sanger sequencing in mouse embryonic stem cells (mESCs). Then, we used SCAN-seq to analyze the mouse preimplantation embryos. We could clearly distinguish cells at different developmental stages, and a total of 27,250 unannotated transcripts from 9,338 genes were identified, with many of which showed developmental stage-specific expression patterns. Finally, we showed that SCAN-seq exhibited high accuracy on determining allele-specific gene expression patterns within an individual cell. SCAN-seq makes a major breakthrough for single-cell transcriptome analysis field

A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy

Abstract Background Oculopharyngodistal myopathy (OPDM) is an autosomal dominant adult-onset degenerative muscle disorder characterized by ptosis, ophthalmoplegia and weakness of the facial, pharyngeal and limb muscles. Trinucleotide repeat expansions in non-coding regions of LRP12, G1PC1, NOTCH2NLC and RILPL1 were reported to be the etiologies for OPDM. Results In this study, we performed long-read whole-genome sequencing in a large five-generation family of 156 individuals, including 21 patients diagnosed with typical OPDM. We identified CGG repeat expansions in 5’UTR of RILPL1 gene in all patients we tested while no CGG expansion in unaffected family members. Repeat-primed PCR and fluorescence amplicon length analysis PCR were further confirmed the segregation of CGG expansions in other family members and 1000 normal Chinese controls. Methylation analysis indicated that methylation levels of the RILPL1 gene were unaltered in OPDM patients, which was consistent with previous studies. Our findings provide evidence that RILPL1 is associated OPDM in this large pedigree. Conclusions Our results identified RILPL1 is the associated the disease in this large pedigree