Rab as well as Arf Grams protein inside endosomal trafficking

An exhaustive literature survey shows that finding protein/gene similarity is an important step towards solving widespread bioinformatics problems. In this article, we have proposed an improved 3-in-1 fused protein similarity measure called FuSim-II. It is built upon combining the weighted average of biological knowledge extracted from three potential genomic/ proteomic resources such as Gene Ontology(GO), PPIN, and protein sequence. Furthermore, we have shown the application of the proposed measure in detecting potential hub-proteins from a given PPIN. Aiming that, we have proposed a multi-objective clustering-based protein hub detection framework with FuSim-II working as the underlying proximity measure. The PPINs of H. Sapiens and M. Musculus organisms are chosen for experimental purposes. Unlike most of the existing hub-detection methods, the proposed technique does not require to follow any protein degree cut-off or threshold to define hubs. A thorough assessment of efficiency between proposed and existing eight protein similarity measures along with eight single/multi-objective clustering methods has been carried out. Also, a comparative performance analysis between proposed and five existing hub-proteins detection algorithms is conducted. The reported results show the improved performance of FuSim-II over existing protein similarity measures in terms of identifying functionally related proteins as well as relevant hub-proteins.Breast cancer is a heterogeneous disease with many clinically distinguishable molecular subtypes each corresponding to a cluster of patients. Identification of prognostic and heterogeneous biomarkers for breast cancer is to detect cluster-specific gene biomarkers which can be used for accurate survival prediction of breast cancer outcomes. In this study, we proposed a FUsion Network-based method (FUNMarker) to identify prognostic and heterogeneous breast cancer biomarkers by considering the heterogeneity of patient samples and biological information from multiple sources. To reduce the affect of heterogeneity of patients, samples were first clustered using the K-means algorithm based on the principal components of gene expression. For each cluster, to comprehensively evaluate the influence of genes on breast cancer, genes were weighted from three aspects biological function, prognostic ability and correlation with known disease genes. Then they were ranked via a label propagation model on a fusion network that combined physical protein interactions from seven types of networks and thus could reduce the impact of incompleteness of interactome. We compared FUNMarker with three state-of-the-art methods and the results showed that biomarkers identified by FUNMarker were biological interpretable and had stronger discriminative power than the existing methods in differentiating patients with different prognostic outcomes.A key aim of post-genomic biomedical research is to systematically understand molecules and their interactions in human cells. Multiple biomolecules coordinate to sustain life activities, and interactions between various biomolecules are interconnected. However, existing studies usually only focusing on associations between two or very limited types of molecules. In this study, we propose a network representation learning based computational framework MAN-SDNE to predict any intermolecular associations. More specifically, we constructed a large-scale molecular association network of multiple biomolecules in human by integrating associations among long non-coding RNA, microRNA, protein, drug, and disease, containing 6,528 molecular nodes, 9 kind of,105,546 associations. And then, the feature of each node is represented by its network proximity and attribute features. Furthermore, these features are used to train Random Forest classifier to predict intermolecular associations. MAN-SDNE achieves a remarkable performance with an AUC of 0.9552 and an AUPR of 0.9338 under five-fold cross-validation. To indicate the ability to predict specific types of interactions, a case study for predicting lncRNA-protein interactions using MAN-SDNE is also executed. Experimental results demonstrate this work offers a systematic insight for understanding the synergistic associations between molecules and complex diseases and provides a network-based computational tool to systematically explore intermolecular interactions.In recent years, sequencing technology has developed rapidly. This produces a large number of biological sequence data. Because of its importance, there have been many studies on biological sequences. However, there is still a lack of an effective quantitative method for defining and calculating texture features of biological sequences. Texture is an important visual feature; it is generally used to describe the spatial arrangement of intensities of images. 10058-F4 in vitro Here we defined the texture features of biological sequence. Combining the digital coding of biological sequence with the calculation method of image texture features, we defined the texture features of biological sequence and designed the calculation method. We applied this method to DNA sequence features quantification and analysis. Using these quantified features, we can compute the similarity distance matrix of DNA sequences and construct the phylogenetic relationships based on the clustering of the quantified features. This method can be applied to analyze any biological sequence, and all biological sequences can be digitally coded and texture features can be calculated by this method. This is a novel study of biological sequence texture features. This will usher in a new era of quantitative and mathematical calculation of biological sequence features.Asynchronous tissue P systems with symport/antiport rules are a class of parallel computing models inspired by cell tissue working in a non-synchronized way, where the use of rules is not obligatory, that is, at a computation step, an enabled rule may or may not be applied. In this work, the notion of local synchronization is introduced at three levels rules, channels, and cells. If a rule in a locally synchronous set of rules (resp., cells or channels) is used, then all enabled rules in the same locally synchronous set of rules (resp., whose involved channels or cells) should be applied in a maximally parallel manner and the implementation of these rules is finished in one computation step. The computational power of local synchronization on asynchronous tissue P systems with symport/antiport rules at the three levels is investigated. It is shown that asynchronous tissue P systems with symport/antiport rules and with locally synchronous sets of rules, channels, or cells are all Turing universal. By comparing the computational power of asynchronous tissue P systems with or without local synchronization, it can be found that the local synchronization is a useful tool to achieve a desired computational power.