Literature DB >> 28873323

Survey of gene splicing algorithms based on reads.

Xiuhua Si1, Qian Wang2, Lei Zhang1, Ruo Wu1, Jiquan Ma1.   

Abstract

Gene splicing is the process of assembling a large number of unordered short sequence fragments to the original genome sequence as accurately as possible. Several popular splicing algorithms based on reads are reviewed in this article, including reference genome algorithms and de novo splicing algorithms (Greedy-extension, Overlap-Layout-Consensus graph, De Bruijn graph). We also discuss a new splicing method based on the MapReduce strategy and Hadoop. By comparing these algorithms, some conclusions are drawn and some suggestions on gene splicing research are made.

Entities:  

Keywords:  De Bruijn graph; Hadoop; MapReduce; gene splicing; read

Mesh:

Year:  2017        PMID: 28873323      PMCID: PMC5736332          DOI: 10.1080/21655979.2017.1373538

Source DB:  PubMed          Journal:  Bioengineered        ISSN: 2165-5979            Impact factor:   3.269


  20 in total

Review 1.  A survey of error-correction methods for next-generation sequencing.

Authors:  Xiao Yang; Sriram P Chockalingam; Srinivas Aluru
Journal:  Brief Bioinform       Date:  2012-04-06       Impact factor: 11.622

2.  SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing.

Authors:  Juliane C Dohm; Claudio Lottaz; Tatiana Borodina; Heinz Himmelbauer
Journal:  Genome Res       Date:  2007-10-01       Impact factor: 9.043

3.  Velvet: algorithms for de novo short read assembly using de Bruijn graphs.

Authors:  Daniel R Zerbino; Ewan Birney
Journal:  Genome Res       Date:  2008-03-18       Impact factor: 9.043

4.  ABySS: a parallel assembler for short read sequence data.

Authors:  Jared T Simpson; Kim Wong; Shaun D Jackman; Jacqueline E Schein; Steven J M Jones; Inanç Birol
Journal:  Genome Res       Date:  2009-02-27       Impact factor: 9.043

5.  Comparison of three targeted enrichment strategies on the SOLiD sequencing platform.

Authors:  Dale J Hedges; Toumy Guettouche; Shan Yang; Guney Bademci; Ashley Diaz; Ashley Andersen; William F Hulme; Sara Linker; Arpit Mehta; Yvonne J K Edwards; Gary W Beecham; Eden R Martin; Margaret A Pericak-Vance; Stephan Zuchner; Jeffery M Vance; John R Gilbert
Journal:  PLoS One       Date:  2011-04-29       Impact factor: 3.240

6.  Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation.

Authors:  Cole Trapnell; Brian A Williams; Geo Pertea; Ali Mortazavi; Gordon Kwan; Marijke J van Baren; Steven L Salzberg; Barbara J Wold; Lior Pachter
Journal:  Nat Biotechnol       Date:  2010-05-02       Impact factor: 54.908

Review 7.  The challenge of small-scale repeats for indel discovery.

Authors:  Giuseppe Narzisi; Michael C Schatz
Journal:  Front Bioeng Biotechnol       Date:  2015-01-26

8.  Swift: primary data analysis for the Illumina Solexa sequencing platform.

Authors:  Nava Whiteford; Tom Skelly; Christina Curtis; Matt E Ritchie; Andrea Löhr; Alexander Wait Zaranek; Irina Abnizova; Clive Brown
Journal:  Bioinformatics       Date:  2009-06-23       Impact factor: 6.937

9.  Crystallizing short-read assemblies around seeds.

Authors:  Mohammad Sajjad Hossain; Navid Azimi; Steven Skiena
Journal:  BMC Bioinformatics       Date:  2009-01-30       Impact factor: 3.169

10.  CloudBurst: highly sensitive read mapping with MapReduce.

Authors:  Michael C Schatz
Journal:  Bioinformatics       Date:  2009-04-08       Impact factor: 6.937

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  1 in total

Review 1.  MicroRNA-mediated bioengineering for climate-resilience in crops.

Authors:  Suraj Patil; Shrushti Joshi; Monica Jamla; Xianrong Zhou; Mohammad J Taherzadeh; Penna Suprasanna; Vinay Kumar
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  1 in total

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