Literature DB >> 34152934

SUVA: splicing site usage variation analysis from RNA-seq data reveals highly conserved complex splicing biomarkers in liver cancer.

Chao Cheng1,2, Lei Liu3, Yongli Bao3, Jingwen Yi3, Weili Quan1, Yaqiang Xue1, Luguo Sun3, Yi Zhang1,2.   

Abstract

Most of the current alternative splicing (AS) analysis tools are powerless to analyse complex splicing. To address this, we developed SUVA (Splice sites Usage Variation Analysis) that decomposes complex splicing events into five types of splice junction pairs. By analysing real and simulated data, SUVA showed higher sensitivity and accuracy in detecting AS events than the compared methods. Notably, SUVA detected extensive complex AS events and screened out 69 highly conserved and dominant AS events associated with cancer. The cancer-associated complex AS events in FN1 and the co-regulated RNA-binding proteins were significantly correlated with patient survival.

Entities:  

Keywords:  Alternative splicing; as; complex splicing; fn1; liver cancer; splicing biomarker; splicing site usage

Mesh:

Substances:

Year:  2021        PMID: 34152934      PMCID: PMC8682974          DOI: 10.1080/15476286.2021.1940037

Source DB:  PubMed          Journal:  RNA Biol        ISSN: 1547-6286            Impact factor:   4.766


  59 in total

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2.  rMATS: robust and flexible detection of differential alternative splicing from replicate RNA-Seq data.

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5.  STAR: ultrafast universal RNA-seq aligner.

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Journal:  Bioinformatics       Date:  2012-10-25       Impact factor: 6.937

6.  Deregulation of alternative splicing of fibronectin pre-mRNA in malignant human liver tumors.

Authors:  F Oyama; S Hirohashi; Y Shimosato; K Titani; K Sekiguchi
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Journal:  Cancer Res       Date:  2008-11-15       Impact factor: 12.701

8.  Identification of recurrent regulated alternative splicing events across human solid tumors.

Authors:  Miri Danan-Gotthold; Regina Golan-Gerstl; Eli Eisenberg; Keren Meir; Rotem Karni; Erez Y Levanon
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9.  HTSeq--a Python framework to work with high-throughput sequencing data.

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Journal:  Bioinformatics       Date:  2014-09-25       Impact factor: 6.937

10.  Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events.

Authors:  Jinfeng Liu; William Lee; Zhaoshi Jiang; Zhongqiang Chen; Suchit Jhunjhunwala; Peter M Haverty; Florian Gnad; Yinghui Guan; Houston N Gilbert; Jeremy Stinson; Christiaan Klijn; Joseph Guillory; Deepali Bhatt; Steffan Vartanian; Kimberly Walter; Jocelyn Chan; Thomas Holcomb; Peter Dijkgraaf; Stephanie Johnson; Julie Koeman; John D Minna; Adi F Gazdar; Howard M Stern; Klaus P Hoeflich; Thomas D Wu; Jeff Settleman; Frederic J de Sauvage; Robert C Gentleman; Richard M Neve; David Stokoe; Zora Modrusan; Somasekar Seshagiri; David S Shames; Zemin Zhang
Journal:  Genome Res       Date:  2012-10-02       Impact factor: 9.043

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  2 in total

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2.  LncRNA TP53TG1 plays an anti-oncogenic role in cervical cancer by synthetically regulating transcriptome profile in HeLa cells.

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