Literature DB >> 26529712

Vials: Visualizing Alternative Splicing of Genes.

Hendrik Strobelt, Bilal Alsallakh, Joseph Botros, Brant Peterson, Mark Borowsky, Hanspeter Pfister, Alexander Lex.   

Abstract

Alternative splicing is a process by which the same DNA sequence is used to assemble different proteins, called protein isoforms. Alternative splicing works by selectively omitting some of the coding regions (exons) typically associated with a gene. Detection of alternative splicing is difficult and uses a combination of advanced data acquisition methods and statistical inference. Knowledge about the abundance of isoforms is important for understanding both normal processes and diseases and to eventually improve treatment through targeted therapies. The data, however, is complex and current visualizations for isoforms are neither perceptually efficient nor scalable. To remedy this, we developed Vials, a novel visual analysis tool that enables analysts to explore the various datasets that scientists use to make judgments about isoforms: the abundance of reads associated with the coding regions of the gene, evidence for junctions, i.e., edges connecting the coding regions, and predictions of isoform frequencies. Vials is scalable as it allows for the simultaneous analysis of many samples in multiple groups. Our tool thus enables experts to (a) identify patterns of isoform abundance in groups of samples and (b) evaluate the quality of the data. We demonstrate the value of our tool in case studies using publicly available datasets.

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Year:  2016        PMID: 26529712      PMCID: PMC4720991          DOI: 10.1109/TVCG.2015.2467911

Source DB:  PubMed          Journal:  IEEE Trans Vis Comput Graph        ISSN: 1077-2626            Impact factor:   4.579


  24 in total

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Review 2.  Understanding alternative splicing: towards a cellular code.

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Review 3.  What is a gene, post-ENCODE? History and updated definition.

Authors:  Mark B Gerstein; Can Bruce; Joel S Rozowsky; Deyou Zheng; Jiang Du; Jan O Korbel; Olof Emanuelsson; Zhengdong D Zhang; Sherman Weissman; Michael Snyder
Journal:  Genome Res       Date:  2007-06       Impact factor: 9.043

4.  Sircah: a tool for the detection and visualization of alternative transcripts.

Authors:  Eoghan D Harrington; Peer Bork
Journal:  Bioinformatics       Date:  2008-07-17       Impact factor: 6.937

5.  Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing.

Authors:  Qun Pan; Ofer Shai; Leo J Lee; Brendan J Frey; Benjamin J Blencowe
Journal:  Nat Genet       Date:  2008-11-02       Impact factor: 38.330

6.  bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death.

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Review 7.  RNA-Seq: a revolutionary tool for transcriptomics.

Authors:  Zhong Wang; Mark Gerstein; Michael Snyder
Journal:  Nat Rev Genet       Date:  2009-01       Impact factor: 53.242

8.  Periostin shows increased evolutionary plasticity in its alternatively spliced region.

Authors:  Sebastian Hoersch; Miguel A Andrade-Navarro
Journal:  BMC Evol Biol       Date:  2010-01-28       Impact factor: 3.260

9.  Alternative isoform regulation in human tissue transcriptomes.

Authors:  Eric T Wang; Rickard Sandberg; Shujun Luo; Irina Khrebtukova; Lu Zhang; Christine Mayr; Stephen F Kingsmore; Gary P Schroth; Christopher B Burge
Journal:  Nature       Date:  2008-11-27       Impact factor: 49.962

10.  TopHat: discovering splice junctions with RNA-Seq.

Authors:  Cole Trapnell; Lior Pachter; Steven L Salzberg
Journal:  Bioinformatics       Date:  2009-03-16       Impact factor: 6.937

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  7 in total

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Journal:  Brief Bioinform       Date:  2020-12-01       Impact factor: 11.622

2.  Manananggal - a novel viewer for alternative splicing events.

Authors:  Matthias Barann; Ralf Zimmer; Fabian Birzele
Journal:  BMC Bioinformatics       Date:  2017-02-21       Impact factor: 3.169

3.  SpliceDetector: a software for detection of alternative splicing events in human and model organisms directly from transcript IDs.

Authors:  Mandana Baharlou Houreh; Payam Ghorbani Kalkhajeh; Ali Niazi; Faezeh Ebrahimi; Esmaeil Ebrahimie
Journal:  Sci Rep       Date:  2018-03-22       Impact factor: 4.379

4.  TSVdb: a web-tool for TCGA splicing variants analysis.

Authors:  Wenjie Sun; Ting Duan; Panmeng Ye; Kelie Chen; Guanling Zhang; Maode Lai; Honghe Zhang
Journal:  BMC Genomics       Date:  2018-05-29       Impact factor: 3.969

5.  Visualization and analysis of RNA-Seq assembly graphs.

Authors:  Fahmi W Nazarie; Barbara Shih; Tim Angus; Mark W Barnett; Sz-Hau Chen; Kim M Summers; Karsten Klein; Geoffrey J Faulkner; Harpreet K Saini; Mick Watson; Stijn van Dongen; Anton J Enright; Tom C Freeman
Journal:  Nucleic Acids Res       Date:  2019-08-22       Impact factor: 16.971

6.  Tasks, Techniques, and Tools for Genomic Data Visualization.

Authors:  S Nusrat; T Harbig; N Gehlenborg
Journal:  Comput Graph Forum       Date:  2019-07-10       Impact factor: 2.078

7.  CAS-viewer: web-based tool for splicing-guided integrative analysis of multi-omics cancer data.

Authors:  Seonggyun Han; Dongwook Kim; Youngjun Kim; Kanghoon Choi; Jason E Miller; Dokyoon Kim; Younghee Lee
Journal:  BMC Med Genomics       Date:  2018-04-20       Impact factor: 3.063

  7 in total

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