Predicting Worst-Case Execution Time Trends in Long-Lived Real-Time Systems

In some long-lived real-time systems, it is not uncommon to see that the execution times of some tasks may exhibit trends. For hard and firm real-time systems, it is important to ensure these trends will not jeopardize the system. In this paper, we first introduce the notion of dynamic worst-case execution time (dWCET), which forms a new perspective that could help a system to predict potential timing failures and optimize resource allocations. We then have a comprehensive review of trend prediction methods. In the evaluation, we make a comparative study of dWCET trend prediction. Four prediction methods, combined with three data selection processes, are applied in an evaluation framework. The result shows the importance of applying data preprocessing and suggests that non-parametric estimators perform better than parametric methods

Pan-cancer analysis of whole genomes

Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe

Evidence for common features in G7 macroeconomic time series

Systems of economic data potentially exhibit a number of common features, which aid both econometric modelling and economic interpretation. This paper surveys a variety of common features and applies the corresponding testing and estimation techniques to systems of macroeconomic time series in the G7 countries. Strong evidence is found of common trends and common or co-dependent cycles in the data, and, for two countries, empirical support for common non-linearities.