Literature DB >> 23995391

Consed: a graphical editor for next-generation sequencing.

David Gordon1, Phil Green.   

Abstract

SUMMARY: The rapid growth of DNA sequencing throughput in recent years implies that graphical interfaces for viewing and correcting errors must now handle large numbers of reads, efficiently pinpoint regions of interest and automate as many tasks as possible. We have adapted consed to reflect this. To allow full-feature editing of large datasets while keeping memory requirements low, we developed a viewer, bamScape, that reads billion-read BAM files, identifies and displays problem areas for user review and launches the consed graphical editor on user-selected regions, allowing, in addition to longstanding consed capabilities such as assembly editing, a variety of new features including direct editing of the reference sequence, variant and error detection, display of annotation tracks and the ability to simultaneously process a group of reads. Many batch processing capabilities have been added. AVAILABILITY: The consed package is free to academic, government and non-profit users, and licensed to others for a fee by the University of Washington. The current version (26.0) is available for linux, macosx and solaris systems or as C++ source code. It includes a user's manual (with exercises) and example datasets. http://www.phrap.org/consed/consed.html CONTACT: dgordon@uw.edu .

Entities:  

Mesh:

Year:  2013        PMID: 23995391      PMCID: PMC3810858          DOI: 10.1093/bioinformatics/btt515

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  17 in total

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2.  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

3.  Mapping short DNA sequencing reads and calling variants using mapping quality scores.

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Journal:  Genome Res       Date:  2008-08-19       Impact factor: 9.043

Review 4.  Next-generation DNA sequencing methods.

Authors:  Elaine R Mardis
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

5.  Viewing and editing assembled sequences using Consed.

Authors:  David Gordon
Journal:  Curr Protoc Bioinformatics       Date:  2003-08

6.  Base-calling of automated sequencer traces using phred. II. Error probabilities.

Authors:  B Ewing; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

7.  Consed: a graphical tool for sequence finishing.

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

8.  Automated finishing with autofinish.

Authors:  D Gordon; C Desmarais; P Green
Journal:  Genome Res       Date:  2001-04       Impact factor: 9.043

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

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Journal:  Bioinformatics       Date:  2009-05-18       Impact factor: 6.937

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

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