There has been an exponential growth in the performance and output of sequencing technologies (omics data) with full genome sequencing now producing gigabases of reads on a daily basis. These data may hold the promise of personalized medicine, leading to routinely available sequencing tests that can guide patient treatment decisions. In the era of high-throughput sequencing (HTS), computational considerations, data governance and clinical translation are the greatest rate-limiting steps. To ensure that the analysis, management and interpretation of such extensive omics data is exploited to its full potential, key factors, including sample sourcing, technology selection and computational expertise and resources, need to be considered, leading to an integrated set of high-performance tools and systems. This article provides an up-to-date overview of the evolution of HTS and the accompanying tools, infrastructure and data management approaches that are emerging in this space, which, if used within in a multidisciplinary context, may ultimately facilitate the development of personalized medicine.

Methane is one of the major contributors to global warming. The rumen microbiota is directly involved in methane production in cattle. The link between variation in rumen microbial communities and host genetics has important applications and implications in bioscience. Having the potential to reveal the full extent of microbial gene diversity and complex microbial interactions, integrated metagenomics and network analysis holds great promise in this endeavour. This study investigates the rumen microbial community in cattle through the integration of metagenomic and network-based approaches. Based on the relative abundance of 1570 microbial genes identified in a metagenomics analysis, the co-abundance network was constructed and functional modules of microbial genes were identified. One of the main contributions is to develop a random matrix theory-based approach to automatically determining the correlation threshold used to construct the co-abundance network. The resulting network, consisting of 549 microbial genes and 3349 connections, exhibits a clear modular structure with certain trait-specific genes highly over-represented in modules. More specifically, all the 20 genes previously identified to be associated with methane emissions are found in a module (hypergeometric test, p<10). One third of genes are involved in methane metabolism pathways. The further examination of abundance profiles across 8 samples of genes highlights that the revealed pattern of metagenomics abundance has a strong association with methane emissions. Furthermore, the module is significantly enriched with microbial genes encoding enzymes that are directly involved in methanogenesis (hypergeometric test, p<10).

Protein-protein interactions (PPI) play a key role in many biological systems. Over the past few years, an explosion in availability of functional biological data obtained from high-throughput technologies to infer PPI has been observed. However, results obtained from such experiments show high rates of false positives and false negatives predictions as well as systematic predictive bias. Recent research has revealed that several machine and statistical learning methods applied to integrate relatively weak, diverse sources of large-scale functional data may provide improved predictive accuracy and coverage of PPI. In this paper we describe the effects of applying different computational, integrative methods to predict PPI in Saccharomyces cerevisiae. We investigated the predictive ability of combining different sets of relatively strong and weak predictive datasets. We analysed several genomic datasets ranging from mRNA co-expression to marginal essentiality. Moreover, we expanded an existing multi-source dataset from S. cerevisiae by constructing a new set of putative interactions extracted from Gene Ontology (GO)-driven annotations in the Saccharomyces Genome Database. Different classification techniques: Simple Naive Bayesian (SNB), Multilayer Perceptron (MLP) and K-Nearest Neighbors (KNN) were evaluated. Relatively simple classification methods (i.e. less computing intensive and mathematically complex), such as SNB, have been proven to be proficient at predicting PPI. SNB produced the "highest" predictive quality obtaining an area under Receiver Operating Characteristic (ROC) curve (AUC) value of 0.99. The lowest AUC value of 0.90 was obtained by the KNN classifier. This assessment also demonstrates the strong predictive power of GO-driven models, which offered predictive performance above 0.90 using the different machine learning and statistical techniques. As the predictive power of single-source datasets became weaker MLP and SNB performed better than KNN. Moreover, predictive performance saturation may be reached independently of the classification models applied, which may be explained by predictive bias and incompleteness of existing "Gold Standards". More comprehensive and accurate PPI maps will be produced for S. cerevisiae and beyond with the emergence of largescale datasets of better predictive quality and the integration of intelligent classification methods.

A crucial step towards understanding the properties of cellular systems in organisms is to map their network of protein-protein interactions (PPIs) on a proteomic-wide scale completely and as accurately as possible. Uncovering the diverse function of proteins and their interactions within the cell may improve our understanding of disease and provide a basis for the development of novel therapeutic approaches. The development of large-scale high-throughput experiments has resulted in the production of a large volume of data which has aided in the uncovering of PPIs. However, these data are often erroneous and limited in interactome coverage. Therefore, additional experimental and computational methods are required to accelerate the discovery of PPIs. This paper provides a review on the prediction of PPIs addressing key prediction principles and highlighting the common experimental and computational techniques currently employed to infer PPI networks along with relevant studies in the area.

GRIP is developed to retrieve information on protein complex, cellular localisation, and physical and genetic interactions in Saccharomyces cerevisiae. Manual construction of reference datasets can be a time consuming process requiring programming knowledge. GRIP simplifies and speeds up this process by allowing users to automatically construct reference datasets. GRIP is free to access at http://rosalind.infj.ulst.ac.uk/GRIP/.

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The discovery of new medications in a cost-effective manner has become the top priority for many pharmaceutical companies. Despite decades of innovation, many of their processes arguably remain relatively inefficient. One such process is the prediction of biological activity. This paper describes a new deep learning model, capable of conducting a preliminary screening of chemical compounds in-silico. The model has been constructed using a variation autoencoder to generate chemical compound fingerprints, which have been used to create a regression model to predict their LogD property and a classification model to predict binding in selected assays from the ChEMBL dataset. The conducted experiments demonstrate accurate prediction of the properties of chemical compounds only using structural definitions and also provide several opportunities to improve upon this model in the future.

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