Literature DB >> 24058384

Statistical and Computational Methods for High-Throughput Sequencing Data Analysis of Alternative Splicing.

Liang Chen1.   

Abstract

The burgeoning field of high-throughput sequencing significantly improves our ability to understand the complexity of transcriptomes. Alternative splicing, as one of the most important driving forces for transcriptome diversity, can now be studied at an unprecedent resolution. Efficient and powerful computational and statistical methods are in urgent need to facilitate the characterization and quantification of alternative splicing events. Here we discuss methods in splice junction read mapping, and methods in exon-centric or isoform-centric quantification of alternative splicing. In addition, we discuss HITS-CLIP and splicing QTL analyses which are novel high-throughput sequencing based approaches in the dissection of splicing regulation.

Entities:  

Keywords:  Alternative splicing; High-throughput sequencing; RNA-seq; Transcript isoform

Year:  2013        PMID: 24058384      PMCID: PMC3776476          DOI: 10.1007/s12561-012-9064-7

Source DB:  PubMed          Journal:  Stat Biosci        ISSN: 1867-1764


  60 in total

1.  De novo assembly and analysis of RNA-seq data.

Authors:  Gordon Robertson; Jacqueline Schein; Readman Chiu; Richard Corbett; Matthew Field; Shaun D Jackman; Karen Mungall; Sam Lee; Hisanaga Mark Okada; Jenny Q Qian; Malachi Griffith; Anthony Raymond; Nina Thiessen; Timothee Cezard; Yaron S Butterfield; Richard Newsome; Simon K Chan; Rong She; Richard Varhol; Baljit Kamoh; Anna-Liisa Prabhu; Angela Tam; YongJun Zhao; Richard A Moore; Martin Hirst; Marco A Marra; Steven J M Jones; Pamela A Hoodless; Inanc Birol
Journal:  Nat Methods       Date:  2010-10-10       Impact factor: 28.547

2.  SOAP2: an improved ultrafast tool for short read alignment.

Authors:  Ruiqiang Li; Chang Yu; Yingrui Li; Tak-Wah Lam; Siu-Ming Yiu; Karsten Kristiansen; Jun Wang
Journal:  Bioinformatics       Date:  2009-06-03       Impact factor: 6.937

3.  Mapping short DNA sequencing reads and calling variants using mapping quality scores.

Authors:  Heng Li; Jue Ruan; Richard Durbin
Journal:  Genome Res       Date:  2008-08-19       Impact factor: 9.043

Review 4.  Splicing regulation in neurologic disease.

Authors:  Donny D Licatalosi; Robert B Darnell
Journal:  Neuron       Date:  2006-10-05       Impact factor: 17.173

5.  Analysis and design of RNA sequencing experiments for identifying isoform regulation.

Authors:  Yarden Katz; Eric T Wang; Edoardo M Airoldi; Christopher B Burge
Journal:  Nat Methods       Date:  2010-11-07       Impact factor: 28.547

6.  Biases in Illumina transcriptome sequencing caused by random hexamer priming.

Authors:  Kasper D Hansen; Steven E Brenner; Sandrine Dudoit
Journal:  Nucleic Acids Res       Date:  2010-04-14       Impact factor: 16.971

7.  Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts.

Authors:  Jeremy R Sanford; Xin Wang; Matthew Mort; Natalia Vanduyn; David N Cooper; Sean D Mooney; Howard J Edenberg; Yunlong Liu
Journal:  Genome Res       Date:  2008-12-30       Impact factor: 9.043

8.  Optimizing de novo transcriptome assembly from short-read RNA-Seq data: a comparative study.

Authors:  Qiong-Yi Zhao; Yi Wang; Yi-Meng Kong; Da Luo; Xuan Li; Pei Hao
Journal:  BMC Bioinformatics       Date:  2011-12-14       Impact factor: 3.169

9.  H-DBAS: human-transcriptome database for alternative splicing: update 2010.

Authors:  Jun-ichi Takeda; Yutaka Suzuki; Ryuichi Sakate; Yoshiharu Sato; Takashi Gojobori; Tadashi Imanishi; Sumio Sugano
Journal:  Nucleic Acids Res       Date:  2009-12-07       Impact factor: 16.971

10.  Expression of 24,426 human alternative splicing events and predicted cis regulation in 48 tissues and cell lines.

Authors:  John C Castle; Chaolin Zhang; Jyoti K Shah; Amit V Kulkarni; Auinash Kalsotra; Thomas A Cooper; Jason M Johnson
Journal:  Nat Genet       Date:  2008-11-02       Impact factor: 38.330

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  5 in total

1.  Systematic evaluation of differential splicing tools for RNA-seq studies.

Authors:  Arfa Mehmood; Asta Laiho; Mikko S Venäläinen; Aidan J McGlinchey; Ning Wang; Laura L Elo
Journal:  Brief Bioinform       Date:  2020-12-01       Impact factor: 11.622

2.  IsoDOT Detects Differential RNA-isoform Expression/Usage with respect to a Categorical or Continuous Covariate with High Sensitivity and Specificity.

Authors:  Wei Sun; Yufeng Liu; James J Crowley; Ting-Hued Chen; Hua Zhou; Haitao Chu; Shunping Huang; Pei-Fen Kuan; Yuan Li; Darla R Miller; Ginger D Shaw; Yichao Wu; Vasyl Zhabotynsky; Leonard McMillan; Fei Zou; Patrick F Sullivan; Fernando Pardo-Manuel de Villena
Journal:  J Am Stat Assoc       Date:  2015-11-07       Impact factor: 5.033

3.  Comparisons of computational methods for differential alternative splicing detection using RNA-seq in plant systems.

Authors:  Ruolin Liu; Ann E Loraine; Julie A Dickerson
Journal:  BMC Bioinformatics       Date:  2014-12-16       Impact factor: 3.169

4.  Gene set enrichment analysis of RNA-Seq data: integrating differential expression and splicing.

Authors:  Xi Wang; Murray J Cairns
Journal:  BMC Bioinformatics       Date:  2013-04-10       Impact factor: 3.169

5.  FineSplice, enhanced splice junction detection and quantification: a novel pipeline based on the assessment of diverse RNA-Seq alignment solutions.

Authors:  Alberto Gatto; Carlos Torroja-Fungairiño; Francesco Mazzarotto; Stuart A Cook; Paul J R Barton; Fátima Sánchez-Cabo; Enrique Lara-Pezzi
Journal:  Nucleic Acids Res       Date:  2014-02-25       Impact factor: 16.971

  5 in total

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