Literature DB >> 19844229

Sense from sequence reads: methods for alignment and assembly.

Paul Flicek1, Ewan Birney.   

Abstract

The most important first step in understanding next-generation sequencing data is the initial alignment or assembly that determines whether an experiment has succeeded and provides a first glimpse into the results. In parallel with the growth of new sequencing technologies, several algorithms that align or assemble the large data output of today's sequencing machines have been developed. We discuss the current algorithmic approaches and future directions of these fundamental tools and provide specific examples for some commonly used tools.

Mesh:

Year:  2009        PMID: 19844229     DOI: 10.1038/nmeth.1376

Source DB:  PubMed          Journal:  Nat Methods        ISSN: 1548-7091            Impact factor:   28.547


  29 in total

Review 1.  The many faces of sequence alignment.

Authors:  Serafim Batzoglou
Journal:  Brief Bioinform       Date:  2005-03       Impact factor: 11.622

2.  Efficient q-gram filters for finding all epsilon-matches over a given length.

Authors:  Kim R Rasmussen; Jens Stoye; Eugene W Myers
Journal:  J Comput Biol       Date:  2006-03       Impact factor: 1.479

3.  Short read fragment assembly of bacterial genomes.

Authors:  Mark J Chaisson; Pavel A Pevzner
Journal:  Genome Res       Date:  2007-12-14       Impact factor: 9.043

4.  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

5.  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

6.  ZOOM! Zillions of oligos mapped.

Authors:  Hao Lin; Zefeng Zhang; Michael Q Zhang; Bin Ma; Ming Li
Journal:  Bioinformatics       Date:  2008-08-06       Impact factor: 6.937

Review 7.  Computational methods for discovering structural variation with next-generation sequencing.

Authors:  Paul Medvedev; Monica Stanciu; Michael Brudno
Journal:  Nat Methods       Date:  2009-11       Impact factor: 28.547

8.  Linguistics of nucleotide sequences. II: Stationary words in genetic texts and the zonal structure of DNA.

Authors:  P A Pevzner; A A Mironov
Journal:  J Biomol Struct Dyn       Date:  1989-04

9.  ALLPATHS: de novo assembly of whole-genome shotgun microreads.

Authors:  Jonathan Butler; Iain MacCallum; Michael Kleber; Ilya A Shlyakhter; Matthew K Belmonte; Eric S Lander; Chad Nusbaum; David B Jaffe
Journal:  Genome Res       Date:  2008-03-13       Impact factor: 9.043

10.  The need for speed.

Authors:  Paul Flicek
Journal:  Genome Biol       Date:  2009-03-27       Impact factor: 13.583

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  127 in total

1.  Chromatin immunoprecipitation and high-throughput sequencing from paraffin-embedded pathology tissue.

Authors:  Mirco Fanelli; Stefano Amatori; Iros Barozzi; Saverio Minucci
Journal:  Nat Protoc       Date:  2011-11-10       Impact factor: 13.491

2.  Fulcrum: condensing redundant reads from high-throughput sequencing studies.

Authors:  Matthew S Burriesci; Erik M Lehnert; John R Pringle
Journal:  Bioinformatics       Date:  2012-03-13       Impact factor: 6.937

3.  Epigenetics in the human brain.

Authors:  Isaac Houston; Cyril J Peter; Amanda Mitchell; Juerg Straubhaar; Evgeny Rogaev; Schahram Akbarian
Journal:  Neuropsychopharmacology       Date:  2012-05-30       Impact factor: 7.853

Review 4.  Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology.

Authors:  Karl V Voelkerding; Shale Dames; Jacob D Durtschi
Journal:  J Mol Diagn       Date:  2010-09       Impact factor: 5.568

Review 5.  A survey of sequence alignment algorithms for next-generation sequencing.

Authors:  Heng Li; Nils Homer
Journal:  Brief Bioinform       Date:  2010-05-11       Impact factor: 11.622

6.  Ray: simultaneous assembly of reads from a mix of high-throughput sequencing technologies.

Authors:  Sébastien Boisvert; François Laviolette; Jacques Corbeil
Journal:  J Comput Biol       Date:  2010-10-20       Impact factor: 1.479

7.  Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.

Authors:  Shale Dames; Jacob Durtschi; Katherine Geiersbach; Jack Stephens; Karl V Voelkerding
Journal:  J Biomol Tech       Date:  2010-07

8.  Do we need new antibiotics? The search for new targets and new compounds.

Authors:  Jaroslav Spížek; Jitka Novotná; Tomáš Rezanka; Arnold L Demain
Journal:  J Ind Microbiol Biotechnol       Date:  2010-11-18       Impact factor: 3.346

9.  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

Review 10.  Next-generation sequencing in clinical virology: Discovery of new viruses.

Authors:  Sibnarayan Datta; Raghvendra Budhauliya; Bidisha Das; Soumya Chatterjee; Vijay Veer
Journal:  World J Virol       Date:  2015-08-12
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