MOTIVATION: Next-generation sequencing technologies generate millions of short sequence reads, which are usually aligned to a reference genome. In many applications, the key information required for downstream analysis is the number of reads mapping to each genomic feature, for example to each exon or each gene. The process of counting reads is called read summarization. Read summarization is required for a great variety of genomic analyses but has so far received relatively little attention in the literature. RESULTS: We present featureCounts, a read summarization program suitable for counting reads generated from either RNA or genomic DNA sequencing experiments. featureCounts implements highly efficient chromosome hashing and feature blocking techniques. It is considerably faster than existing methods (by an order of magnitude for gene-level summarization) and requires far less computer memory. It works with either single or paired-end reads and provides a wide range of options appropriate for different sequencing applications. AVAILABILITY AND IMPLEMENTATION: featureCounts is available under GNU General Public License as part of the Subread (http://subread.sourceforge.net) or Rsubread (http://www.bioconductor.org) software packages.

featureCounts: an efficient general-purpose program for assigning sequence reads to genomic features

Functional analysis of large gene lists, derived in most cases from emerging high-throughput genomic, proteomic and bioinformatics scanning approaches, is still a challenging and daunting task. The gene-annotation enrichment analysis is a promising high-throughput strategy that increases the likelihood for investigators to identify biological processes most pertinent to their study. Approximately 68 bioinformatics enrichment tools that are currently available in the community are collected in this survey. Tools are uniquely categorized into three major classes, according to their underlying enrichment algorithms. The comprehensive collections, unique tool classifications and associated questions/issues will provide a more comprehensive and up-to-date view regarding the advantages, pitfalls and recent trends in a simpler tool-class level rather than by a tool-by-tool approach. Thus, the survey will help tool designers/developers and experienced end users understand the underlying algorithms and pertinent details of particular tool categories/tools, enabling them to make the best choices for their particular research interests.

/pdf/bioinformatics-enrichment-tools-paths-toward-the-2yo1xl3r2j.pdf

Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

The reference human genome sequence set the stage for studies of genetic variation and its association with human disease, but epigenomic studies lack a similar reference. To address this need, the NIH Roadmap Epigenomics Consortium generated the largest collection so far of human epigenomes for primary cells and tissues. Here we describe the integrative analysis of 111 reference human epigenomes generated as part of the programme, profiled for histone modification patterns, DNA accessibility, DNA methylation and RNA expression. We establish global maps of regulatory elements, define regulatory modules of coordinated activity, and their likely activators and repressors. We show that disease- and trait-associated genetic variants are enriched in tissue-specific epigenomic marks, revealing biologically relevant cell types for diverse human traits, and providing a resource for interpreting the molecular basis of human disease. Our results demonstrate the central role of epigenomic information for understanding gene regulation, cellular differentiation and human disease.

/pdf/integrative-analysis-of-111-reference-human-epigenomes-4bavnjaon6.pdf

Integrative analysis of 111 reference human epigenomes

We present GOseq, an application for performing Gene Ontology (GO) analysis on RNA-seq data. GO analysis is widely used to reduce complexity and highlight biological processes in genome-wide expression studies, but standard methods give biased results on RNA-seq data due to over-detection of differential expression for long and highly expressed transcripts. Application of GOseq to a prostate cancer data set shows that GOseq dramatically changes the results, highlighting categories more consistent with the known biology.

/pdf/gene-ontology-analysis-for-rna-seq-accounting-for-selection-456k6bns5w.pdf

Gene ontology analysis for RNA-seq: accounting for selection bias

Outcomes of high-throughput biological experiments are typically interpreted by statistical testing for enriched gene functional categories defined by the Gene Ontology (GO). The resulting lists of GO terms may be large and highly redundant, and thus difficult to interpret.

REVIGO is a Web server that summarizes long, unintelligible lists of GO terms by finding a representative subset of the terms using a simple clustering algorithm that relies on semantic similarity measures. Furthermore, REVIGO visualizes this non-redundant GO term set in multiple ways to assist in interpretation: multidimensional scaling and graph-based visualizations accurately render the subdivisions and the semantic relationships in the data, while treemaps and tag clouds are also offered as alternative views. REVIGO is freely available at http://revigo.irb.hr/.

/pdf/revigo-summarizes-and-visualizes-long-lists-of-gene-ontology-3taarmiz8n.pdf

REVIGO Summarizes and Visualizes Long Lists of Gene Ontology Terms

Generation and verification of vertical meteorological data for building energy simulation from a 325-meter Beijing meteorological tower

Coupled Tamm plasmon polaritons induced narrow bandpass filter with ultra-wide stopband

Deep reinforcement learning (DRL) has shown good performance in tackling Markov decision process (MDP) problems. As DRL opti-mizes a long-term reward, it is a promising approach to improving the energy efficiency of data center cooling. However, enforcement of thermal safety constraint during DRL's state exploration is a main challenge. The widely adopted reward shaping approach adds negative reward when the exploratory action results in unsafety. Thus, it needs to experience sufficient unsafe states before it learns how to prevent unsafety. In this paper, we propose a safety-aware DRL framework for single-hall data center cooling control. It applies offline imitation learning and online post-hoc rectification to holis-tically prevent thermal unsafety during online DRL. In particular, the post-hoc rectification searches for the minimum modification to the DRL-recommended action such that the rectified action will not result in unsafety. The rectification is designed based on a thermal state transition model that is fitted using historical safe operation traces and able to extrapolate the transitions to unsafe states ex-plored by DRL. Extensive evaluation for chilled water and direct expansion cooled data centers in two climate conditions shows that our approach saves 22.7% to 26.6% total data center power compared with conventional control, reduces safety violations by 94.5% to 99% compared with reward shaping.

/pdf/toward-physics-guided-safe-deep-reinforcement-learning-for-15fnxtw3.pdf

Toward Physics-Guided Safe Deep Reinforcement Learning for Green Data Center Cooling Control

Impacts of uncertainty in building envelope thermal transmittance on heating/cooling demand in the urban context

Colorectal cancer (CRC) has become the second deadliest cancer in the world and severely threatens human health. An increasing number of studies have focused on the role of the RNA helicase DEAD-box (DDX) family in CRC. However, the mechanism of DDX10 in CRC has not been elucidated.In our study, we analysed the expression data of CRC samples from the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) databases. Subsequently, we performed cytological experiments and animal experiments to explore the role of DDX10 in CRC cells. Furthermore, we performed Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis and protein-protein interaction (PPI) network analyses. Finally, we predicted the interacting protein of DDX10 by LC-MS/MS and verified it by coimmunoprecipitation (Co-IP) and qPCR.In the present study, we identified that DDX10 mRNA was extremely highly expressed in CRC tissues compared with normal colon tissues in the TCGA and GEO databases. The protein expression of DDX10 was measured by immunochemistry (IHC) in 17 CRC patients. The biological roles of DDX10 were explored via cell and molecular biology experiments in vitro and in vivo and cell cycle assays. We found that DDX10 knockdown markedly reduced CRC cell proliferation, migration and invasion. Then, we constructed a PPI network with the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING). GO and KEGG enrichment analysis and gene set enrichment analysis (GSEA) showed that DDX10 was closely related to RNA splicing and E2F targets. Using LC-MS/MS and Co-IP assays, we discovered that RPL35 is the interacting protein of DDX10. In addition, we hypothesize that RPL35 is related to the E2F pathway and the immune response in CRC.In conclusion, provides a better understanding of the molecular mechanisms of DDX10 in CRC and provides a potential biomarker for the diagnosis and treatment of CRC. 

/pdf/ddx10-promotes-the-proliferation-and-metastasis-of-1znrl6dk.pdf

Xin Zhou

Papers

Generation and verification of vertical meteorological data for building energy simulation from a 325-meter Beijing meteorological tower

Coupled Tamm plasmon polaritons induced narrow bandpass filter with ultra-wide stopband

Toward Physics-Guided Safe Deep Reinforcement Learning for Green Data Center Cooling Control

Impacts of uncertainty in building envelope thermal transmittance on heating/cooling demand in the urban context

DDX10 promotes the proliferation and metastasis of colorectal cancer cells via splicing RPL35