Literature DB >> 19679872

LookSeq: a browser-based viewer for deep sequencing data.

Heinrich Magnus Manske1, Dominic P Kwiatkowski.   

Abstract

Sequencing a genome to great depth can be highly informative about heterogeneity within an individual or a population. Here we address the problem of how to visualize the multiple layers of information contained in deep sequencing data. We propose an interactive AJAX-based web viewer for browsing large data sets of aligned sequence reads. By enabling seamless browsing and fast zooming, the LookSeq program assists the user to assimilate information at different levels of resolution, from an overview of a genomic region to fine details such as heterogeneity within the sample. A specific problem, particularly if the sample is heterogeneous, is how to depict information about structural variation. LookSeq provides a simple graphical representation of paired sequence reads that is more revealing about potential insertions and deletions than are conventional methods.

Mesh:

Year:  2009        PMID: 19679872      PMCID: PMC2775587          DOI: 10.1101/gr.093443.109

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  23 in total

1.  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

2.  Accurate multiplex polony sequencing of an evolved bacterial genome.

Authors:  Jay Shendure; Gregory J Porreca; Nikos B Reppas; Xiaoxia Lin; John P McCutcheon; Abraham M Rosenbaum; Michael D Wang; Kun Zhang; Robi D Mitra; George M Church
Journal:  Science       Date:  2005-08-04       Impact factor: 47.728

3.  Genome sequencing in microfabricated high-density picolitre reactors.

Authors:  Marcel Margulies; Michael Egholm; William E Altman; Said Attiya; Joel S Bader; Lisa A Bemben; Jan Berka; Michael S Braverman; Yi-Ju Chen; Zhoutao Chen; Scott B Dewell; Lei Du; Joseph M Fierro; Xavier V Gomes; Brian C Godwin; Wen He; Scott Helgesen; Chun Heen Ho; Chun He Ho; Gerard P Irzyk; Szilveszter C Jando; Maria L I Alenquer; Thomas P Jarvie; Kshama B Jirage; Jong-Bum Kim; James R Knight; Janna R Lanza; John H Leamon; Steven M Lefkowitz; Ming Lei; Jing Li; Kenton L Lohman; Hong Lu; Vinod B Makhijani; Keith E McDade; Michael P McKenna; Eugene W Myers; Elizabeth Nickerson; John R Nobile; Ramona Plant; Bernard P Puc; Michael T Ronan; George T Roth; Gary J Sarkis; Jan Fredrik Simons; John W Simpson; Maithreyan Srinivasan; Karrie R Tartaro; Alexander Tomasz; Kari A Vogt; Greg A Volkmer; Shally H Wang; Yong Wang; Michael P Weiner; Pengguang Yu; Richard F Begley; Jonathan M Rothberg
Journal:  Nature       Date:  2005-07-31       Impact factor: 49.962

4.  Whole-genome sequencing and variant discovery in C. elegans.

Authors:  LaDeana W Hillier; Gabor T Marth; Aaron R Quinlan; David Dooling; Ginger Fewell; Derek Barnett; Paul Fox; Jarret I Glasscock; Matthew Hickenbotham; Weichun Huang; Vincent J Magrini; Ryan J Richt; Sacha N Sander; Donald A Stewart; Michael Stromberg; Eric F Tsung; Todd Wylie; Tim Schedl; Richard K Wilson; Elaine R Mardis
Journal:  Nat Methods       Date:  2008-01-20       Impact factor: 28.547

5.  A sequence assembly and editing program for efficient management of large projects.

Authors:  S Dear; R Staden
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

6.  Consed: a graphical tool for sequence finishing.

Authors:  D Gordon; C Abajian; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

7.  A new DNA sequence assembly program.

Authors:  J K Bonfield; K f Smith; R Staden
Journal:  Nucleic Acids Res       Date:  1995-12-25       Impact factor: 16.971

8.  The Sequence Alignment/Map format and SAMtools.

Authors:  Heng Li; Bob Handsaker; Alec Wysoker; Tim Fennell; Jue Ruan; Nils Homer; Gabor Marth; Goncalo Abecasis; Richard Durbin
Journal:  Bioinformatics       Date:  2009-06-08       Impact factor: 6.937

9.  Hawkeye: an interactive visual analytics tool for genome assemblies.

Authors:  Michael C Schatz; Adam M Phillippy; Ben Shneiderman; Steven L Salzberg
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583

10.  High-throughput sequence alignment using Graphics Processing Units.

Authors:  Michael C Schatz; Cole Trapnell; Arthur L Delcher; Amitabh Varshney
Journal:  BMC Bioinformatics       Date:  2007-12-10       Impact factor: 3.169

View more
  41 in total

Review 1.  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

Review 2.  Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Authors:  Elizabeth T Cirulli; David B Goldstein
Journal:  Nat Rev Genet       Date:  2010-06       Impact factor: 53.242

Review 3.  Visualizing genomes: techniques and challenges.

Authors:  Cydney B Nielsen; Michael Cantor; Inna Dubchak; David Gordon; Ting Wang
Journal:  Nat Methods       Date:  2010-02-25       Impact factor: 28.547

Review 4.  The utility of genomic data for Plasmodium vivax population surveillance.

Authors:  Rachel F Daniels; Benjamin L Rice; Noah M Daniels; Sarah K Volkman; Daniel L Hartl
Journal:  Pathog Glob Health       Date:  2015-04-18       Impact factor: 2.894

Review 5.  From next-generation resequencing reads to a high-quality variant data set.

Authors:  S P Pfeifer
Journal:  Heredity (Edinb)       Date:  2016-10-19       Impact factor: 3.821

6.  Next generation sequencing in cardiovascular diseases.

Authors:  Francesca Faita; Cecilia Vecoli; Ilenia Foffa; Maria Grazia Andreassi
Journal:  World J Cardiol       Date:  2012-10-26

Review 7.  High throughput sequencing approaches to mutation discovery in the mouse.

Authors:  Michelle M Simon; Ann-Marie Mallon; Gareth R Howell; Laura G Reinholdt
Journal:  Mamm Genome       Date:  2012-09-19       Impact factor: 2.957

8.  MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation.

Authors:  Huabin Hou; Fangqing Zhao; Linglin Zhou; Erle Zhu; Huajing Teng; Xiaokun Li; Qiyu Bao; Jinyu Wu; Zhongsheng Sun
Journal:  Nucleic Acids Res       Date:  2010-05-05       Impact factor: 16.971

9.  Gap5--editing the billion fragment sequence assembly.

Authors:  James K Bonfield; Andrew Whitwham
Journal:  Bioinformatics       Date:  2010-05-30       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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.