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Consed: A Graphical Tool for Sequence Finishing
Author(s) -
David Gordon,
Chris Abajian,
Phil Green
Publication year - 1998
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.8.3.195
Subject(s) - contig , sequence assembly , bottleneck , shotgun sequencing , biology , hybrid genome assembly , genome , computational biology , sequence (biology) , correctness , reference genome , process (computing) , alignment free sequence analysis , computer science , sequence tagged site , genetics , sequence alignment , algorithm , programming language , gene , chromosome , gene mapping , gene expression , transcriptome , peptide sequence , embedded system
Sequencing of large clones or small genomes is generally done by the shotgun approach (Anderson et al. 1982). This has two phases: (1) a shotgun phase in which a number of reads are generated from random subclones and assembled into contigs, followed by (2) a directed, or finishing phase in which the assembly is inspected for correctness and for various kinds of data anomalies (such as contaminant reads, unremoved vector sequence, and chimeric or deleted reads), additional data are collected to close gaps and resolve low quality regions, and editing is performed to correct assembly or base-calling errors. Finishing is currently a bottleneck in large-scale sequencing efforts, and throughput gains will depend both on reducing the need for human intervention and making it as efficient as possible. We have developed a finishing tool, consed, which attempts to implement these principles. A distinguishing feature relative to other programs is the use of error probabilities from our programs phred and phrap as an objective criterion to guide the entire finishing process. More information is available at http:// www.genome.washington.edu/consed/consed. html.

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