Tongji University

About: Tongji University is a education organization based out in Shanghai, China. It is known for research contribution in the topics: Computer science & Population. The organization has 76116 authors who have published 81176 publications receiving 1248911 citations. The organization is also known as: Tongji & Tóngjì Dàxué.

Computational systems biology.

Abstract: The complex biological systems consist of distinct molecules that exert their functions by interacting with each other, which makes it a big challenge to understand how the cellular machinery works. Recently, the accumulation of a large amount of multiscale omics data, such as next-generation sequencing data and protein interaction data, provides opportunity to investigate the functions of molecules from a systematic perspective. On the other hand, the analysis of these huge datasets demands efficient and robust computational methods. In this special issue, we reported the recent progress made in developing new computational methodologies to analyze the genomics data, construct gene networks, and identify disease genes. Understanding the Functions of Molecules in the Postgenomic Age. In recent years, the advance of next-generation sequencing (NGS) technology makes it more easier for researchers to access and analyze genetics data and has influential effects on the biomedical research community. However, compared with sequencing, computational analysis of the flooding sequencing data with appropriate tools is becoming a more important task when interpreting the data. In their review paper, M. P. Dolled-Filhart et al. described the pipeline for bioinformatics analysis of the NGS data, starting from alignment to variant calling as well as filtering and annotation. In each step, they discussed the tools or software that should be used as well as their advantages and caveats. This survey of the bioinformatics analysis of NGS data can help researchers to choose appropriate tools when dealing with the sequencing data. Along with the sequencing technology, lines of evidence show that a lot of noncoding RNAs (ncRNAs) play important roles in various biological processes. Unlike the protein-coding genes that are well studied, the functions of most ncRNAs are not clear. Therefore, it is highly desirable to develop computational methods to predict the functions of the ncRNAs. H. Ma et al. conducted a survey about the computational approaches developed to predict and annotate the long noncoding RNAs (lncRNAs), which can help researchers to learn the progress in this filed and future directions in which bioinformaticists should work while annotating lncRNAs. While annotating the functions of molecules, standard and controlled vocabularies are required. Hence, the ontologies that are represented as abstract description systems of knowledge are becoming more and more popular recently. At the same time, it is becoming a difficult task to calculate the semantic similarity between ontology terms quantitatively. M. Gan et al. introduced popular methods in quantitating the semantic similarity between ontology terms and their software implementations. Furthermore, they classified these methods into distinct categories and discussed their advantages and shortcomings, which can help researchers to select appropriate tools and methods when working on ontologies. Gene expression profiles can describe the molecular mechanisms that underlie certain phenotypes. However, while analyzing the gene expression data, it is inappropriate to treat genes independently considering genes interact with each other within the cell. O. Frings et al. proposed a network-based approach to analyze the gene expression data and applied it to investigate the development of sex-specific chicken gonad and brain tissues. By combining the chicken network and the gene expression data, they identified some sex-biased characteristics, for example, same sex-biased genes tend to be tightly connected in the network, and provided new insights into the molecular underpinnings of sex-biased genes. Construction and Analysis of Gene Networks. Construction of gene regulatory networks (GRNs) is a crucial step in systems biology, where gene expression data is widely explored to infer the GRNs. However, the high dimensionality and notorious noise of the gene expression data makes it a nontrivial task to infer the GRNs. N. You et al. presented a new Laplace error penalty (LEP) model to calculate the partial correlation coefficients between genes and construct the GRNs. Compared with the popular least absolute shrinkage and selection operator (LASSO) and smoothly clipped absolute deviation (SCAD) approaches, the LEP method reached the highest precision. Except for gene expression data, integration of different data sources may improve the accuracy of inferred GRNs. H. Chen et al. surveyed the strategies to integrate distinct data sources and their effectiveness and recommended how to choose an appropriate strategy while integrating distinct data sources. N. Nakajima et al. proposed a novel network completion approach, DPLSQ, to infer gene networks. Benchmarking on artificial datasets, their proposed DPLSQ outperforms popular ARACNE and GeneNet with the highest accuracy. By investigating a 2-gene network, A. V. Spirov et al. found that gene cooption can affect the robustness of GRNs, and the findings provide new insights into the evolvability and robustness of GRNs. Network modules are found to be functional blocks of gene networks, the identification of which is becoming a hot research topic. By taking the hierarchical modular structure into account, S. Zhang presented a new stochastic block model to detect the hierarchical modules. Applied to the real yeast gene coexpression network, the proposed method can efficiently detect the hierarchical modular structures that are consistent with biological functions. Recently, it is found that a particular type of ncRNAs, microRNAs, plays important roles in gene regulation by working together with transcription factors. W. Mu et al. proposed a new local genetic algorithm to predict condition-specific regulatory modules that consist of microRNAs, transcription factors, and their commonly regulated genes, and these modules provide useful insights into the regulatory mechanisms underlying gene expression. Computational Approaches to Hunting Disease-Associated Genes. The identification of genetic variants that are responsible for human diseases is critical for understanding the development of diseases and designing new effective drugs. Thanks to the genome-wide association studies (GWASs), some genetic variants that drive diseases have been identified, among which single nucleotide polymorphisms (SNPs) and nonsynonymous single nucleotide polymorphisms (nsSNPs) are receiving more and more attention. In this issue, J. Wu and R. Jiang reviewed the databases that collect nsSNPs and summarized popular computational methods that identify deleterious nsSNPs. In addition, they introduced machine learning models that are useful in predicting deleterious nsSNPs. Beyond SNP-based association analysis, gene-based association analysis is receiving increasing attention. X. Guo et al. comprehensively compared these two approaches on the data from the study of addiction and found that these two approaches complement with each other and can get better results when used together. The differentially expressed genes identified from microarray data are generally regarded as candidate disease genes. However, the number of differentially expressed genes may reach hundreds or even thousands, thereby making it difficult to identify the potential disease genes. In this issue, L. Li et al. proposed a new hybrid approach to predict disease genes based on estimation of distribution algorithm and support vector machine. Benchmarking on B-cell lymphoma and colon cancer datasets, their method outperforms two other popular approaches and identify some new candidate genes for future validation.

Sparse R-CNN: End-to-End Object Detection with Learnable Proposals

Abstract: We present Sparse R-CNN, a purely sparse method for object detection in images. Existing works on object detection heavily rely on dense object candidates, such as $k$ anchor boxes pre-defined on all grids of image feature map of size $H\times W$. In our method, however, a fixed sparse set of learned object proposals, total length of $N$, are provided to object recognition head to perform classification and location. By eliminating $HWk$ (up to hundreds of thousands) hand-designed object candidates to $N$ (e.g. 100) learnable proposals, Sparse R-CNN completely avoids all efforts related to object candidates design and many-to-one label assignment. More importantly, final predictions are directly output without non-maximum suppression post-procedure. Sparse R-CNN demonstrates accuracy, run-time and training convergence performance on par with the well-established detector baselines on the challenging COCO dataset, e.g., achieving 45.0 AP in standard $3\times$ training schedule and running at 22 fps using ResNet-50 FPN model. We hope our work could inspire re-thinking the convention of dense prior in object detectors. The code is available at: https://github.com/PeizeSun/SparseR-CNN.

Vandetanib plus docetaxel versus docetaxel as second-line treatment for patients with advanced non-small-cell lung cancer (ZODIAC): a double-blind, randomised, phase 3 trial.

Abstract: Summary Background Vandetanib is a once-daily oral inhibitor of vascular endothelial growth factor receptor (VEGFR), epidermal growth factor receptor (EGFR), and rearranged during transfection (RET) tyrosine kinases. In a randomised phase 2 study in patients with previously treated non-small-cell lung cancer (NSCLC), adding vandetanib 100 mg to docetaxel significantly improved progression-free survival (PFS) compared with docetaxel alone, including a longer PFS in women. These results supported investigation of the combination in this larger, definitive phase 3 trial (ZODIAC). Methods Between May, 2006, and April, 2008, patients with locally advanced or metastatic (stage IIIB–IV) NSCLC after progression following first-line chemotherapy were randomly assigned 1:1 through a third-party interactive voice system to receive vandetanib (100 mg/day) plus docetaxel (75 mg/m 2 intravenously every 21 days; maximum six cycles) or placebo plus docetaxel. The primary objective was comparison of PFS between the two groups in the intention-to-treat population. Women were a coprimary analysis population. This study has been completed and is registered with ClinicalTrials.gov, number NCT00312377. Findings 1391 patients received vandetanib plus docetaxel (n=694 [197 women]) or placebo plus docetaxel (n=697 [224 women]). Vandetanib plus docetaxel led to a significant improvement in PFS versus placebo plus docetaxel (hazard ratio [HR] 0·79, 97·58% CI 0·70–0·90; p vs 7/690 [1%]), neutropenia (199/689 [29%] vs 164/690 [24%]), leukopenia (99/689 [14%] vs 77/690 [11%]), and febrile neutropenia (61/689 [9%] vs 48/690 [7%]) were more common with vandetanib plus docetaxel than with placebo plus docetaxel. The most common serious adverse event was febrile neutropenia (46/689 [7%] in the vandetanib group vs 38/690 [6%] in the placebo group). Interpretation The addition of vandetanib to docetaxel provides a significant improvement in PFS in patients with advanced NSCLC after progression following first-line therapy. Funding AstraZeneca.

Observation of Pseudocapacitive Effect and Fast Ion Diffusion in Bimetallic Sulfides as an Advanced Sodium-Ion Battery Anode

Abstract: Lithium-ion batteries (LIBs) have permeated energy storage market from portable electronics to electric vehicles in view of their high energy density and long cycle life.[1] Nevertheless, it is still expensive to scale up due to the limited Li sources.[2] In contrast, sodium-ion batteries (SIBs), with similar energy Sodium-ion batteries (SIBs) are promising next-generation alternatives due to the low cost and abundance of sodium sources. Yet developmental electrodes in SIBs such as transition metal sulfides have huge volume expansion, sluggish Na+ diffusion kinetics, and poor electrical conductivity. Here bimetallic sulfide (Co9S8/ZnS) nanocrystals embedded in hollow nitrogen-doped carbon nanosheets are demonstrated with a high sodium diffusion coefficient, pseudocapacitive effect, and excellent reversibility. Such a unique composite structure is designed and synthesized via a facile sulfidation of the CoZn-MOFs followed by calcination and is highly dependant on the reaction time and temperature. The optimized Co1Zn1-S(600) electrode exhibits excellent sodium storage performance, including a high capacity of 542 mA h g−1 at 0.1 A g−1, good rate capability at 10 A g−1, and excellent cyclic stability up to 500 cycles for half-cell. It also shows potential in full-cell configuration. Such capabilities will accelerate the adoption of sodium-ion batteries for electrical energy applications.

Lattice Dislocations Enhancing Thermoelectric PbTe in Addition to Band Convergence

Abstract: Phonon scattering by nanostructures and point defects has become the primary strategy for minimizing the lattice thermal conductivity (κL ) in thermoelectric materials. However, these scatterers are only effective at the extremes of the phonon spectrum. Recently, it has been demonstrated that dislocations are effective at scattering the remaining mid-frequency phonons as well. In this work, by varying the concentration of Na in Pb0.97 Eu0.03 Te, it has been determined that the dominant microstructural features are point defects, lattice dislocations, and nanostructure interfaces. This study reveals that dense lattice dislocations (≈4 × 1012 cm-2 ) are particularly effective at reducing κL . When the dislocation concentration is maximized, one of the lowest κL values reported for PbTe is achieved. Furthermore, due to the band convergence of the alloyed 3% mol. EuTe the electronic performance is enhanced, and a high thermoelectric figure of merit, zT, of ≈2.2 is achieved. This work not only demonstrates the effectiveness of dense lattice dislocations as a means of lowering κL , but also the importance of engineering both thermal and electronic transport simultaneously when designing high-performance thermoelectrics.