Genome Research · 1998 · 3.3K citations · 10 references
Life SciencesBioinformaticsBiologyGenome AssemblyGenomicsSequence AnalysisContig ConstructionDna SequencingGenome SequencingSequence AssemblySequence Quality ControlSequencingBase CallingContig AssemblyContig RefinementDe Novo Assembly FinishingRead Quality ControlSequencing Error CorrectionShotgun SequencingThroughput
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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Base-Calling of Automated Sequencer Traces Using<i>Phred.</i> I. Accuracy Assessment
Brent Ewing, LaDeana Hillier, Michael C. Wendl et al. · Genome Research · 1998 · 7K citations · Full text
A new DNA sequence assembly program
James Bonfield, Kathryn F. Smith, Rodger Staden · Nucleic Acids Research · 1995 · 985 citations · Full text