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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2015
    In:  Genome Biology Vol. 16, No. 1 ( 2015-12)
    In: Genome Biology, Springer Science and Business Media LLC, Vol. 16, No. 1 ( 2015-12)
    Type of Medium: Online Resource
    ISSN: 1474-760X
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2015
    detail.hit.zdb_id: 2040529-7
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2023
    In:  Bioinformatics Vol. 39, No. 1 ( 2023-01-01)
    In: Bioinformatics, Oxford University Press (OUP), Vol. 39, No. 1 ( 2023-01-01)
    Abstract: igv.js is an embeddable JavaScript implementation of the Integrative Genomics Viewer (IGV). It can be easily dropped into any web page with a single line of code and has no external dependencies. The viewer runs completely in the web browser, with no backend server and no data pre-processing required. Availability and implementation The igv.js JavaScript component can be installed from NPM at https://www.npmjs.com/package/igv. The source code is available at https://github.com/igvteam/igv.js under the MIT open-source license. IGV-Web, the end-user application built around igv.js, is available at https://igv.org/app. The source code is available at https://github.com/igvteam/igv-webapp under the MIT open-source license. Supplementary information Supplementary information is available at Bioinformatics online.
    Type of Medium: Online Resource
    ISSN: 1367-4811
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
    detail.hit.zdb_id: 1468345-3
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  • 3
    In: F1000Research, F1000 Research Ltd, Vol. 6 ( 2018-1-30), p. 784-
    Type of Medium: Online Resource
    ISSN: 2046-1402
    Language: English
    Publisher: F1000 Research Ltd
    Publication Date: 2018
    detail.hit.zdb_id: 2699932-8
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  • 4
    Online Resource
    Online Resource
    Elsevier BV ; 2017
    In:  Cell Systems Vol. 5, No. 2 ( 2017-08), p. 149-151.e1
    In: Cell Systems, Elsevier BV, Vol. 5, No. 2 ( 2017-08), p. 149-151.e1
    Type of Medium: Online Resource
    ISSN: 2405-4712
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2854138-8
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  • 5
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2011
    In:  Nature Biotechnology Vol. 29, No. 1 ( 2011-1), p. 24-26
    In: Nature Biotechnology, Springer Science and Business Media LLC, Vol. 29, No. 1 ( 2011-1), p. 24-26
    Type of Medium: Online Resource
    ISSN: 1087-0156 , 1546-1696
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2011
    detail.hit.zdb_id: 1494943-X
    detail.hit.zdb_id: 1311932-1
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 1988
    In:  Journal of Molecular Graphics Vol. 6, No. 4 ( 1988-12), p. 223-
    In: Journal of Molecular Graphics, Elsevier BV, Vol. 6, No. 4 ( 1988-12), p. 223-
    Type of Medium: Online Resource
    ISSN: 0263-7855
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1988
    detail.hit.zdb_id: 2158199-X
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  • 7
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2017
    In:  Cancer Research Vol. 77, No. 13_Supplement ( 2017-07-01), p. 2588-2588
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 77, No. 13_Supplement ( 2017-07-01), p. 2588-2588
    Abstract: As the availability of genetic and genomic data and analysis tools from large-scale cancer initiatives continues to increase, the need has become more urgent for a software environment that supports the entire “idea to dissemination” cycle of an integrative cancer genomics analysis. Such a system would need to provide access to a large number of analysis tools without the need for programming, be sufficiently flexible to accommodate the practices of non-programming biologists as well as experienced bioinformaticians, and would provide a way for researchers to encapsulate their work into a single “executable document” including not only the analytical workflow but also the associated descriptive text, graphics, and supporting research. To address these needs, we have developed GenePattern Notebook, based on the GenePattern environment for integrative genomics and the Jupyter Notebook system. GenePattern Notebook unites the phases of in silico research – experiment design, collaborative analysis, and publication – into a single interface. GenePattern Notebook presents a familiar lab-notebook format that allows researchers to build a record of their work by creating “cells” containing text, graphics, or executable analyses. Researchers add, delete, and modify cells as the research evolves, supporting the initial research phases of prototyping and collaborative analysis. When an analysis is ready for publication, the same document that was used in the design and analysis phases becomes a research narrative that interleaves text, graphics, data, and executable analyses, serving as the complete, reproducible, in silico methods section for a publication. GenePattern Notebook features are designed to make it easy for nonprogramming users to create and adapt notebooks. We have developed new cell types that allow users to choose analyses, specify input parameters and datasets, navigate results, send result files to new analyses, and create richly formatted text, all without the need for programming. We have released a freely available online GenePattern Notebook workspace, http://notebook.genepattern.org, where researchers can develop and publish notebook documents. We have provided a collection of template notebooks that walk users through various machine learning analyses, and are collaborating with cancer research laboratories to create integrative cancer genomics notebooks as well. Notebook topics in development include characterization of intratumoral heterogeneity from single cell RNA-Seq data, effective clinical interpretation of comprehensive genomic profiling from whole exome sequencing of a patient’s tumor and germ line samples, and identification of master regulators/transcription factors associated with the downstream transcriptional effects associated with the activation of an oncogene. Citation Format: Michael M. Reich, Thorin T. Tabor, Ted Liefeld, Barbara Hill, Helga Thorvaldsdottir, Jill P. Mesirov. GenePattern Notebook: an environment for reproducible cancer research [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 2588. doi:10.1158/1538-7445.AM2017-2588
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2017
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 8
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2020
    In:  Cancer Research Vol. 80, No. 16_Supplement ( 2020-08-15), p. 3207-3207
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 80, No. 16_Supplement ( 2020-08-15), p. 3207-3207
    Abstract: As the availability of genetic and genomic data and analysis tools from large-scale cancer initiatives continues to increase, with single-cell studies adding new dimensions to the potential scientific insights, the need has become more urgent for a software environment that supports the rapid pace of cancer data science. The electronic analysis notebook has recently emerged as an effective and versatile tool for this purpose, allowing scientists to combine the scientific exposition – text, images, and multimedia – with the actual code that runs the analysis, creating a single “research narrative” document. The Jupyter Notebook system has become the de facto standard notebook environment in data science and genomic analysis. However, the Jupyter environment requires familiarity with a programming language to run analyses, and even text must be formatted using a programming-style language. To extend notebook capabilities to the needs of researchers at all levels of programming expertise, we developed the GenePattern Notebook environment, which integrates Jupyter's capabilities with the hundreds of genomic tools available through the GenePattern platform. This tool allows scientists to develop, share, collaborate on, and publish their notebooks, requiring only a web browser. In this environment, investigators can design their in-silico experiments, perform and refine analyses, launch compute-intensive analyses on cloud-based and high-performance compute resources, and publish their results as electronic notebooks that other scientists can adopt to reproduce the original analyses and modify for their own work. GenePattern Notebook provides: (1) Access to a wide range of genomic analyses within a notebook. Hundreds of analyses are available, from machine learning techniques such as clustering, classification, and dimension reduction, to omic-specific methods for gene expression analysis, proteomics, flow cytometry, sequence variation analysis, pathway analysis, and others. (2) A library of featured genomic analysis notebooks is provided. These include templates for common analysis tasks as well as cancer-specific research scenarios and compute-intensive methods. Scientists can easily copy these notebooks, use them as is, or adapt them for their research purposes. (3) Notebook enhancements. A rich text editor allows scientists to enter and format text as they would in a word processor. A user interface-building tool allows notebook developers to wrap their code so it is displayed as a web form, with only the necessary inputs exposed. Users of the notebook are presented with a simplified display that allows them to run the analyses without needing to interact with the code behind them. (4) Publication and collaborative editing. To make a notebook public, an author selects the “publish” feature and adds descriptive information. The notebook is then made available on the community section of the notebook workspace. An author can include a web link to a public notebook in a publication, and users who follow the link will see a read-only version of the notebook, with the option to log in to the workspace, where they can run, copy, and edit their own version. The GenePattern Notebook environment is freely available at http://genepattern-notebook.org. Citation Format: Michael M. Reich, Thorin Tabor, Ted Liefeld, Edwin Juarez, Barbara Hill, Helga Thorvaldsdottir, Pablo Tamayo, Jill P. Mesirov. GenePattern Notebook: An integrative analytical environment for cancer research [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 3207.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 9
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2023
    In:  Cancer Research Vol. 83, No. 7_Supplement ( 2023-04-04), p. 2073-2073
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 83, No. 7_Supplement ( 2023-04-04), p. 2073-2073
    Abstract: As the availability of genomic data and analysis tools from large-scale cancer initiatives continues to increase, with single-cell studies adding new dimensions to the potential scientific insights, the need has become more urgent for a software environment that supports the rapid pace of cancer data science. The The Jupyter Notebook environment has become the de facto medium for this purpose due to its ease in combining scientific exposition with executable code to form a single reproducible “research narrative” document. However, analyses are often compute-intensive, requiring more resources than are frequently available within a notebook environment running on a desktop or laptop computer. Additionally, thousands of tools, modules, and plugins are readily available on integrative software platforms such as Galaxy, GenePattern, and Cytoscape, outside the notebook paradigm. Finally, many biomedical investigators lack the programming expertise required to fully realize the benefits and utility of the notebook metaphor. To address these issues, we have released Genomics to Notebook (g2nb), which builds on JupyterLab to add access to bioinformatics platforms and other functionality for the non-programmer through the components described below, while retaining all programmatic features of JupyterLab.The g2nb environment incorporates bioinformatics software platforms within the notebook interface, allowing a single notebook to contain a workflow spanning multiple tools and servers. When run, the entire analysis appears to execute seamlessly within the notebook. To achieve this, we developed a new analysis cell type that provides an interface within the notebook to tools that are hosted on a remote Galaxy or GenePattern server. Analysis cells present a web form-like interface, similar to that of the original platforms, requiring an investigator to provide only the input parameters and data. The popular visualization tools Cytoscape and Integrative Genomics Viewer (IGV) are also supported in their web-based formats as notebook cells, with additional platforms and visualizers added regularly. The g2nb environment is freely available at the g2nb workspace, http://g2nb.org, where scientists can use all of the g2nb functionality with only a web browser. Those who wish to use g2nb locally can use the provided Docker container or install the packages via the conda or pip package managers. The online workspace also includes a library of featured genomic analysis notebooks, including templates for common analysis tasks as well as cancer-specific research scenarios and compute-intensive methods. Scientists can easily copy these notebooks, use them as is, or adapt them for their research purposes. Citation Format: Michael M. Reich, Thorin Tabor, John Liefeld, Jayadev Joshi, Forrest Kim, Helga Thorvaldsdottir, Daniel Blankenberg, Jill P. Mesirov. Genomics to Notebook (g2nb): Extending the electronic notebook to address the needs of cancer bioinformatics [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2023; Part 1 (Regular and Invited Abstracts); 2023 Apr 14-19; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2023;83(7_Suppl):Abstract nr 2073.
    Type of Medium: Online Resource
    ISSN: 1538-7445
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2023
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2011
    In:  Bioinformatics Vol. 27, No. 12 ( 2011-06-15), p. 1739-1740
    In: Bioinformatics, Oxford University Press (OUP), Vol. 27, No. 12 ( 2011-06-15), p. 1739-1740
    Abstract: Motivation: Well-annotated gene sets representing the universe of the biological processes are critical for meaningful and insightful interpretation of large-scale genomic data. The Molecular Signatures Database (MSigDB) is one of the most widely used repositories of such sets. Results: We report the availability of a new version of the database, MSigDB 3.0, with over 6700 gene sets, a complete revision of the collection of canonical pathways and experimental signatures from publications, enhanced annotations and upgrades to the web site. Availability and Implementation: MSigDB is freely available for non-commercial use at http://www.broadinstitute.org/msigdb. Contact:  gsea@broadinstitute.org
    Type of Medium: Online Resource
    ISSN: 1367-4811 , 1367-4803
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2011
    detail.hit.zdb_id: 1468345-3
    SSG: 12
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