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      TIMEOR: a web-based tool to uncover temporal regulatory mechanisms from multi-omics data

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          Abstract

          Uncovering how transcription factors regulate their targets at DNA, RNA and protein levels over time is critical to define gene regulatory networks (GRNs) and assign mechanisms in normal and diseased states. RNA-seq is a standard method measuring gene regulation using an established set of analysis stages. However, none of the currently available pipeline methods for interpreting ordered genomic data (in time or space) use time-series models to assign cause and effect relationships within GRNs, are adaptive to diverse experimental designs, or enable user interpretation through a web-based platform. Furthermore, methods integrating ordered RNA-seq data with protein–DNA binding data to distinguish direct from indirect interactions are urgently needed. We present TIMEOR (Trajectory Inference and Mechanism Exploration with Omics data in R), the first web-based and adaptive time-series multi-omics pipeline method which infers the relationship between gene regulatory events across time. TIMEOR addresses the critical need for methods to determine causal regulatory mechanism networks by leveraging time-series RNA-seq, motif analysis, protein–DNA binding data, and protein-protein interaction networks. TIMEOR’s user-catered approach helps non-coders generate new hypotheses and validate known mechanisms. We used TIMEOR to identify a novel link between insulin stimulation and the circadian rhythm cycle. TIMEOR is available at https://github.com/ashleymaeconard/TIMEOR.git and http://timeor.brown.edu.

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          TIMEOR: novel web tool generates gene regulatory network and beyond to assign mechanism combining temporal and multi-omics data.

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          Most cited references56

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          Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

          In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. We present DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. The DESeq2 package is available at http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html. Electronic supplementary material The online version of this article (doi:10.1186/s13059-014-0550-8) contains supplementary material, which is available to authorized users.
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            Trimmomatic: a flexible trimmer for Illumina sequence data

            Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool or combination of tools that met our requirements in terms of flexibility, correct handling of paired-end data and high performance. We have developed Trimmomatic as a more flexible and efficient preprocessing tool, which could correctly handle paired-end data. Results: The value of NGS read preprocessing is demonstrated for both reference-based and reference-free tasks. Trimmomatic is shown to produce output that is at least competitive with, and in many cases superior to, that produced by other tools, in all scenarios tested. Availability and implementation: Trimmomatic is licensed under GPL V3. It is cross-platform (Java 1.5+ required) and available at http://www.usadellab.org/cms/index.php?page=trimmomatic Contact: usadel@bio1.rwth-aachen.de Supplementary information: Supplementary data are available at Bioinformatics online.
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              Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities.

              Genome-scale studies have revealed extensive, cell type-specific colocalization of transcription factors, but the mechanisms underlying this phenomenon remain poorly understood. Here, we demonstrate in macrophages and B cells that collaborative interactions of the common factor PU.1 with small sets of macrophage- or B cell lineage-determining transcription factors establish cell-specific binding sites that are associated with the majority of promoter-distal H3K4me1-marked genomic regions. PU.1 binding initiates nucleosome remodeling, followed by H3K4 monomethylation at large numbers of genomic regions associated with both broadly and specifically expressed genes. These locations serve as beacons for additional factors, exemplified by liver X receptors, which drive both cell-specific gene expression and signal-dependent responses. Together with analyses of transcription factor binding and H3K4me1 patterns in other cell types, these studies suggest that simple combinations of lineage-determining transcription factors can specify the genomic sites ultimately responsible for both cell identity and cell type-specific responses to diverse signaling inputs. Copyright 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                02 July 2021
                14 June 2021
                14 June 2021
                : 49
                : W1
                : W641-W653
                Affiliations
                Computer Science Department, Brown University , Providence, RI 02912, USA
                Center for Computational and Molecular Biology, Brown University , Providence, RI 02912, USA
                Computer Science Department, Brown University , Providence, RI 02912, USA
                Department of Genetics, Harvard Medical School , Boston, MA 02115, USA
                Director of Bioinformatics DRSC/TRiP Functional Genomics Resources, Harvard Medical School , Boston, MA 02115, USA
                Department of Genetics, Harvard Medical School , Boston, MA 02115, USA
                Howard Hughes Medical Institute, Harvard Medical School , Boston, MA 02115, USA
                Computer Science Department, Brown University , Providence, RI 02912, USA
                Center for Computational and Molecular Biology, Brown University , Providence, RI 02912, USA
                Center for Computational and Molecular Biology, Brown University , Providence, RI 02912, USA
                Applied Math Department, Brown University , Providence, RI 02912, USA
                Center for Computational and Molecular Biology, Brown University , Providence, RI 02912, USA
                Department of Molecular Biology, Cell Biology and Biochemistry, Brown University , Providence, RI 02912, USA
                Author notes
                To whom correspondence should be addressed. Tel: +1 765 891 0288; Email: ashley_conard@ 123456brown.edu
                Correspondence may also be addressed to Erica Larschan. Tel: +1 401 863 1070; Fax: +1 401 863 1201; Email: erica_larschan@ 123456brown.edu
                Correspondence may also be addressed to Charles Lawrence. Tel: +1 401 863 1479; Email: charles_lawrence@ 123456brown.edu
                Author information
                https://orcid.org/0000-0002-4143-6180
                https://orcid.org/0000-0003-1494-1402
                https://orcid.org/0000-0001-7542-472X
                https://orcid.org/0000-0002-7523-160X
                https://orcid.org/0000-0003-4011-6692
                Article
                gkab384
                10.1093/nar/gkab384
                8262710
                34125906
                11820f8c-64d2-4c47-9685-9bc66813dc25
                © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 28 April 2021
                : 13 April 2021
                : 05 March 2021
                Page count
                Pages: 13
                Funding
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: 5R35GM126994
                Funded by: National Science Foundation, DOI 10.13039/100000001;
                Funded by: Center for Computational and Molecular Biology;
                Award ID: P20GM109035
                Funded by: National Institute of General Medical Sciences, DOI 10.13039/100000057;
                Categories
                AcademicSubjects/SCI00010
                Web Server Issue

                Genetics
                Genetics

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