Literature DB >> 20460430

A survey of sequence alignment algorithms for next-generation sequencing.

Heng Li1, Nils Homer.   

Abstract

Rapidly evolving sequencing technologies produce data on an unparalleled scale. A central challenge to the analysis of this data is sequence alignment, whereby sequence reads must be compared to a reference. A wide variety of alignment algorithms and software have been subsequently developed over the past two years. In this article, we will systematically review the current development of these algorithms and introduce their practical applications on different types of experimental data. We come to the conclusion that short-read alignment is no longer the bottleneck of data analyses. We also consider future development of alignment algorithms with respect to emerging long sequence reads and the prospect of cloud computing.

Mesh:

Year:  2010        PMID: 20460430      PMCID: PMC2943993          DOI: 10.1093/bib/bbq015

Source DB:  PubMed          Journal:  Brief Bioinform        ISSN: 1467-5463            Impact factor:   11.622


  56 in total

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Authors:  Bin Ma; John Tromp; Ming Li
Journal:  Bioinformatics       Date:  2002-03       Impact factor: 6.937

2.  BLAT--the BLAST-like alignment tool.

Authors:  W James Kent
Journal:  Genome Res       Date:  2002-04       Impact factor: 9.043

3.  SSAHA: a fast search method for large DNA databases.

Authors:  Z Ning; A J Cox; J C Mullikin
Journal:  Genome Res       Date:  2001-10       Impact factor: 9.043

4.  The generic genome browser: a building block for a model organism system database.

Authors:  Lincoln D Stein; Christopher Mungall; ShengQiang Shu; Michael Caudy; Marco Mangone; Allen Day; Elizabeth Nickerson; Jason E Stajich; Todd W Harris; Adrian Arva; Suzanna Lewis
Journal:  Genome Res       Date:  2002-10       Impact factor: 9.043

5.  High quality SNP calling using Illumina data at shallow coverage.

Authors:  Nawar Malhis; Steven J M Jones
Journal:  Bioinformatics       Date:  2010-02-26       Impact factor: 6.937

6.  Identification of common molecular subsequences.

Authors:  T F Smith; M S Waterman
Journal:  J Mol Biol       Date:  1981-03-25       Impact factor: 5.469

7.  Fast and SNP-tolerant detection of complex variants and splicing in short reads.

Authors:  Thomas D Wu; Serban Nacu
Journal:  Bioinformatics       Date:  2010-02-10       Impact factor: 6.937

8.  Versatile and open software for comparing large genomes.

Authors:  Stefan Kurtz; Adam Phillippy; Arthur L Delcher; Michael Smoot; Martin Shumway; Corina Antonescu; Steven L Salzberg
Journal:  Genome Biol       Date:  2004-01-30       Impact factor: 13.583

9.  Fast and accurate long-read alignment with Burrows-Wheeler transform.

Authors:  Heng Li; Richard Durbin
Journal:  Bioinformatics       Date:  2010-01-15       Impact factor: 6.937

10.  BamView: viewing mapped read alignment data in the context of the reference sequence.

Authors:  Tim Carver; Ulrike Böhme; Thomas D Otto; Julian Parkhill; Matthew Berriman
Journal:  Bioinformatics       Date:  2010-01-12       Impact factor: 6.937

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  247 in total

1.  Maize HapMap2 identifies extant variation from a genome in flux.

Authors:  Jer-Ming Chia; Chi Song; Peter J Bradbury; Denise Costich; Natalia de Leon; John Doebley; Robert J Elshire; Brandon Gaut; Laura Geller; Jeffrey C Glaubitz; Michael Gore; Kate E Guill; Jim Holland; Matthew B Hufford; Jinsheng Lai; Meng Li; Xin Liu; Yanli Lu; Richard McCombie; Rebecca Nelson; Jesse Poland; Boddupalli M Prasanna; Tanja Pyhäjärvi; Tingzhao Rong; Rajandeep S Sekhon; Qi Sun; Maud I Tenaillon; Feng Tian; Jun Wang; Xun Xu; Zhiwu Zhang; Shawn M Kaeppler; Jeffrey Ross-Ibarra; Michael D McMullen; Edward S Buckler; Gengyun Zhang; Yunbi Xu; Doreen Ware
Journal:  Nat Genet       Date:  2012-06-03       Impact factor: 38.330

2.  ChIP-Seq: technical considerations for obtaining high-quality data.

Authors:  Benjamin L Kidder; Gangqing Hu; Keji Zhao
Journal:  Nat Immunol       Date:  2011-09-20       Impact factor: 25.606

3.  Mapping rare and common causal alleles for complex human diseases.

Authors:  Soumya Raychaudhuri
Journal:  Cell       Date:  2011-09-30       Impact factor: 41.582

4.  Adaptive seeds tame genomic sequence comparison.

Authors:  Szymon M Kiełbasa; Raymond Wan; Kengo Sato; Paul Horton; Martin C Frith
Journal:  Genome Res       Date:  2011-01-05       Impact factor: 9.043

5.  Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR.

Authors:  Hui Yang; Kai Wang
Journal:  Nat Protoc       Date:  2015-09-17       Impact factor: 13.491

6.  Canonical, stable, general mapping using context schemes.

Authors:  Adam M Novak; Yohei Rosen; David Haussler; Benedict Paten
Journal:  Bioinformatics       Date:  2015-07-27       Impact factor: 6.937

7.  PAPNC, a novel method to calculate nucleotide diversity from large scale next generation sequencing data.

Authors:  Wei Shao; Mary F Kearney; Valerie F Boltz; Jonathan E Spindler; John W Mellors; Frank Maldarelli; John M Coffin
Journal:  J Virol Methods       Date:  2014-03-26       Impact factor: 2.014

Review 8.  ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions.

Authors:  Terrence S Furey
Journal:  Nat Rev Genet       Date:  2012-10-23       Impact factor: 53.242

9.  Detecting rare variants for psychiatric disorders using next generation sequencing: a methods primer.

Authors:  Andre Altmann; Carina Quast; Peter Weber
Journal:  Curr Psychiatry Rep       Date:  2013-01       Impact factor: 5.285

Review 10.  Clinical analysis and interpretation of cancer genome data.

Authors:  Eliezer M Van Allen; Nikhil Wagle; Mia A Levy
Journal:  J Clin Oncol       Date:  2013-04-15       Impact factor: 44.544

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