Literature DB >> 34506690

Exploring the Genomic Landscape of Cancer Patient Cohorts with GenVisR.

Zachary L Skidmore1,2, Katie M Campbell1,2, Kelsy C Cotto1,2, Malachi Griffith1,2,3,4, Obi L Griffith1,2,3,4.   

Abstract

The creation of visualizations to interpret genomics data remains an important aspect of data science within computational biology. The GenVisR Bioconductor package was created to lower the entry point for publication-quality graphics and has remained a popular suite of tools within this domain. GenVisR supports visualizations covering a breadth of topics including functions to produce visual summaries of copy-number alterations, somatic variants, sequence quality metrics, and more. Recently, the GenVisR package has undergone significant updates to increase performance and functionality. To demonstrate the utility of GenVisR, we present protocols for use of the updated Waterfall() function to create a customizable Oncoprint-style plot of the mutational landscape of a tumor cohort. We explain the basics of installation, data import, configuration, plotting, clinical annotation, and customization. A companion online workshop describing the GenVisR library, Waterfall() function, and other genomic visualization tools is available at genviz.org.
© 2021 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Generating a Waterfall() plot from original mutation data Basic Protocol 2: Adding clinical data to a Waterfall() plot Basic Protocol 3: Customizing mutation burden in Waterfall() plots Basic Protocol 4: Brief exploration of customizable options Support Protocol 1: Installing GenVisR. © 2021 The Authors. Current Protocols published by Wiley Periodicals LLC.

Entities:  

Keywords:  Bioconductor; R; genome visualization

Mesh:

Year:  2021        PMID: 34506690      PMCID: PMC8439545          DOI: 10.1002/cpz1.252

Source DB:  PubMed          Journal:  Curr Protoc        ISSN: 2691-1299


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Journal:  Mod Pathol       Date:  2011-10-21       Impact factor: 7.842

6.  Genome Modeling System: A Knowledge Management Platform for Genomics.

Authors:  Malachi Griffith; Obi L Griffith; Scott M Smith; Avinash Ramu; Matthew B Callaway; Anthony M Brummett; Michael J Kiwala; Adam C Coffman; Allison A Regier; Ben J Oberkfell; Gabriel E Sanderson; Thomas P Mooney; Nathaniel G Nutter; Edward A Belter; Feiyu Du; Robert L Long; Travis E Abbott; Ian T Ferguson; David L Morton; Mark M Burnett; James V Weible; Joshua B Peck; Adam Dukes; Joshua F McMichael; Justin T Lolofie; Brian R Derickson; Jasreet Hundal; Zachary L Skidmore; Benjamin J Ainscough; Nathan D Dees; William S Schierding; Cyriac Kandoth; Kyung H Kim; Charles Lu; Christopher C Harris; Nicole Maher; Christopher A Maher; Vincent J Magrini; Benjamin S Abbott; Ken Chen; Eric Clark; Indraniel Das; Xian Fan; Amy E Hawkins; Todd G Hepler; Todd N Wylie; Shawn M Leonard; William E Schroeder; Xiaoqi Shi; Lynn K Carmichael; Matthew R Weil; Richard W Wohlstadter; Gary Stiehr; Michael D McLellan; Craig S Pohl; Christopher A Miller; Daniel C Koboldt; Jason R Walker; James M Eldred; David E Larson; David J Dooling; Li Ding; Elaine R Mardis; Richard K Wilson
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Journal:  Plant Biotechnol J       Date:  2018-05-31       Impact factor: 9.803

8.  The Ensembl Variant Effect Predictor.

Authors:  William McLaren; Laurent Gil; Sarah E Hunt; Harpreet Singh Riat; Graham R S Ritchie; Anja Thormann; Paul Flicek; Fiona Cunningham
Journal:  Genome Biol       Date:  2016-06-06       Impact factor: 13.583

9.  Maftools: efficient and comprehensive analysis of somatic variants in cancer.

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10.  Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer.

Authors:  Alex H Wagner; Siddhartha Devarakonda; Zachary L Skidmore; Kilannin Krysiak; Avinash Ramu; Lee Trani; Jason Kunisaki; Ashiq Masood; Saiama N Waqar; Nicholas C Spies; Daniel Morgensztern; Jason Waligorski; Jennifer Ponce; Robert S Fulton; Leonard B Maggi; Jason D Weber; Mark A Watson; Christopher J O'Conor; Jon H Ritter; Rachelle R Olsen; Haixia Cheng; Anandaroop Mukhopadhyay; Ismail Can; Melissa H Cessna; Trudy G Oliver; Elaine R Mardis; Richard K Wilson; Malachi Griffith; Obi L Griffith; Ramaswamy Govindan
Journal:  Nat Commun       Date:  2018-09-17       Impact factor: 14.919

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  1 in total

1.  Comprehensive Analysis of HMCN1 Somatic Mutation in Clear Cell Renal Cell Carcinoma.

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  1 in total

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