Literature DB >> 24524156

Genome-guided transcriptome assembly in the age of next-generation sequencing.

Liliana D Florea, Steven L Salzberg.   

Abstract

Next-generation sequencing technologies provide unprecedented power to explore the repertoire of genes and their alternative splice variants, collectively defining the transcriptome of a species in great detail. However, assembling the short reads into full-length gene and transcript models presents significant computational challenges. We review current algorithms for assembling transcripts and genes from next-generation sequencing reads aligned to a reference genome, and lay out areas for future improvements.

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Year:  2013        PMID: 24524156      PMCID: PMC4086730          DOI: 10.1109/tcbb.2013.140

Source DB:  PubMed          Journal:  IEEE/ACM Trans Comput Biol Bioinform        ISSN: 1545-5963            Impact factor:   3.710


  30 in total

Review 1.  Alternative splicing: increasing diversity in the proteomic world.

Authors:  B R Graveley
Journal:  Trends Genet       Date:  2001-02       Impact factor: 11.639

2.  Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain.

Authors:  Adam Ameur; Ammar Zaghlool; Jonatan Halvardson; Anna Wetterbom; Ulf Gyllensten; Lucia Cavelier; Lars Feuk
Journal:  Nat Struct Mol Biol       Date:  2011-11-06       Impact factor: 15.369

3.  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

4.  Gene and alternative splicing annotation with AIR.

Authors:  Liliana Florea; Valentina Di Francesco; Jason Miller; Russell Turner; Alison Yao; Michael Harris; Brian Walenz; Clark Mobarry; Gennady V Merkulov; Rosane Charlab; Ian Dew; Zuoming Deng; Sorin Istrail; Peter Li; Granger Sutton
Journal:  Genome Res       Date:  2005-01       Impact factor: 9.043

5.  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

Review 6.  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

7.  Oases: robust de novo RNA-seq assembly across the dynamic range of expression levels.

Authors:  Marcel H Schulz; Daniel R Zerbino; Martin Vingron; Ewan Birney
Journal:  Bioinformatics       Date:  2012-02-24       Impact factor: 6.937

8.  Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences.

Authors:  Jeremy Goecks; Anton Nekrutenko; James Taylor
Journal:  Genome Biol       Date:  2010-08-25       Impact factor: 13.583

9.  iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq data.

Authors:  Aziz M Mezlini; Eric J M Smith; Marc Fiume; Orion Buske; Gleb L Savich; Sohrab Shah; Sam Aparicio; Derek Y Chiang; Anna Goldenberg; Michael Brudno
Journal:  Genome Res       Date:  2012-11-29       Impact factor: 9.043

10.  OLego: fast and sensitive mapping of spliced mRNA-Seq reads using small seeds.

Authors:  Jie Wu; Olga Anczuków; Adrian R Krainer; Michael Q Zhang; Chaolin Zhang
Journal:  Nucleic Acids Res       Date:  2013-04-09       Impact factor: 16.971

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  4 in total

Review 1.  Advances in genetics and genomics: use and limitations in achieving malaria elimination goals.

Authors:  Sharmini Gunawardena; Nadira D Karunaweera
Journal:  Pathog Glob Health       Date:  2015-05       Impact factor: 2.894

2.  CLASS2: accurate and efficient splice variant annotation from RNA-seq reads.

Authors:  Li Song; Sarven Sabunciyan; Liliana Florea
Journal:  Nucleic Acids Res       Date:  2016-03-14       Impact factor: 16.971

3.  High resolution annotation of zebrafish transcriptome using long-read sequencing.

Authors:  German Nudelman; Antonio Frasca; Brandon Kent; Kirsten C Sadler; Stuart C Sealfon; Martin J Walsh; Elena Zaslavsky
Journal:  Genome Res       Date:  2018-07-30       Impact factor: 9.043

4.  MEOX2 Transcription Factor Is Involved in Survival and Adhesion of Glioma Stem-like Cells.

Authors:  Gaëlle Tachon; Konstantin Masliantsev; Pierre Rivet; Amandine Desette; Serge Milin; Elise Gueret; Michel Wager; Lucie Karayan-Tapon; Pierre-Olivier Guichet
Journal:  Cancers (Basel)       Date:  2021-11-25       Impact factor: 6.639

  4 in total

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