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      State of the Field in Multi-Omics Research: From Computational Needs to Data Mining and Sharing

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          Abstract

          Multi-omics, variously called integrated omics, pan-omics, and trans-omics, aims to combine two or more omics data sets to aid in data analysis, visualization and interpretation to determine the mechanism of a biological process. Multi-omics efforts have taken center stage in biomedical research leading to the development of new insights into biological events and processes. However, the mushrooming of a myriad of tools, datasets, and approaches tends to inundate the literature and overwhelm researchers new to the field. The aims of this review are to provide an overview of the current state of the field, inform on available reliable resources, discuss the application of statistics and machine/deep learning in multi-omics analyses, discuss findable, accessible, interoperable, reusable (FAIR) research, and point to best practices in benchmarking. Thus, we provide guidance to interested users of the domain by addressing challenges of the underlying biology, giving an overview of the available toolset, addressing common pitfalls, and acknowledging current methods’ limitations. We conclude with practical advice and recommendations on software engineering and reproducibility practices to share a comprehensive awareness with new researchers in multi-omics for end-to-end workflow.

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          Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal.

          The cBioPortal for Cancer Genomics (http://cbioportal.org) provides a Web resource for exploring, visualizing, and analyzing multidimensional cancer genomics data. The portal reduces molecular profiling data from cancer tissues and cell lines into readily understandable genetic, epigenetic, gene expression, and proteomic events. The query interface combined with customized data storage enables researchers to interactively explore genetic alterations across samples, genes, and pathways and, when available in the underlying data, to link these to clinical outcomes. The portal provides graphical summaries of gene-level data from multiple platforms, network visualization and analysis, survival analysis, patient-centric queries, and software programmatic access. The intuitive Web interface of the portal makes complex cancer genomics profiles accessible to researchers and clinicians without requiring bioinformatics expertise, thus facilitating biological discoveries. Here, we provide a practical guide to the analysis and visualization features of the cBioPortal for Cancer Genomics.
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            The FAIR Guiding Principles for scientific data management and stewardship

            There is an urgent need to improve the infrastructure supporting the reuse of scholarly data. A diverse set of stakeholders—representing academia, industry, funding agencies, and scholarly publishers—have come together to design and jointly endorse a concise and measureable set of principles that we refer to as the FAIR Data Principles. The intent is that these may act as a guideline for those wishing to enhance the reusability of their data holdings. Distinct from peer initiatives that focus on the human scholar, the FAIR Principles put specific emphasis on enhancing the ability of machines to automatically find and use the data, in addition to supporting its reuse by individuals. This Comment is the first formal publication of the FAIR Principles, and includes the rationale behind them, and some exemplar implementations in the community.
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              NCBI GEO: archive for functional genomics data sets—update

              The Gene Expression Omnibus (GEO, http://www.ncbi.nlm.nih.gov/geo/) is an international public repository for high-throughput microarray and next-generation sequence functional genomic data sets submitted by the research community. The resource supports archiving of raw data, processed data and metadata which are indexed, cross-linked and searchable. All data are freely available for download in a variety of formats. GEO also provides several web-based tools and strategies to assist users to query, analyse and visualize data. This article reports current status and recent database developments, including the release of GEO2R, an R-based web application that helps users analyse GEO data.
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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                10 December 2020
                2020
                : 11
                : 610798
                Affiliations
                [1] 1Nuffield Department of Women’s & Reproductive Health, University of Oxford , Oxford, United Kingdom
                [2] 2Novo Nordisk Research Center Seattle, Inc , Seattle, WA, United States
                [3] 3Independent Researcher , Bengaluru, India
                [4] 4Independent Researcher , Namburu, India
                Author notes

                Edited by: Fatemeh Maghuly, University of Natural Resources and Life Sciences, Vienna, Austria

                Reviewed by: Heinz Himmelbauer, University of Natural Resources and Life Sciences, Vienna, Austria; Subina Mehta, University of Minnesota Twin Cities, United States; Wan M. Aizat, National University of Malaysia, Malaysia

                *Correspondence: Biswapriya B. Misra, bbmisraccb@ 123456gmail.com

                ORCID: Michal Krassowski, orcid.org/0000-0002-9638-7785; Vivek Das, orcid.org/0000-0003-0614-0373; Sangram K. Sahu, orcid.org/0000-0001-5010-9539; Biswapriya B. Misra, orcid.org/0000-0003-2589-6539

                This article was submitted to Systems Biology, a section of the journal Frontiers in Genetics

                Article
                10.3389/fgene.2020.610798
                7758509
                33362867
                cfb32b5a-6549-4697-8b01-ff8202e75843
                Copyright © 2020 Krassowski, Das, Sahu and Misra.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 September 2020
                : 20 November 2020
                Page count
                Figures: 5, Tables: 2, Equations: 0, References: 103, Pages: 17, Words: 0
                Categories
                Genetics
                Review

                Genetics
                machine learning,benchmarking,fair,integrated omics,multi-omics,reproducibility,visualization,data heterogeneity

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