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• Introduction
  • Genome finishing and working with shared data
  • Contact information
  • System requirements
  • Installing modules
    • Licensing modules
    • Uninstalling modules
  • Installing server extensions
    • Licensing server extensions
• Align Contigs
  • How to run the Align Contigs tool
  • How to use the Align Contigs tool
    • The Contig table
    • The Contig match table
    • Joining two contigs
    • Splitting a contig
    • Adding new data
• Analyze Contigs
  • How to run the Analyze Contigs tool
  • How to use the Analyze Contigs tool
    • The contig analysis table
    • How to edit data following contig analysis
• Create Amplicons
  • How to run the Create Amplicons tool
• Create Primers
  • How to use the Create Primers tool
    • Create Primers output
    • Primer scoring
    • Temperature calculation
• Add Reads to Contigs
  • How to run the Add reads to contigs
• Find Sequence
  • How to run the Find Sequence tool
    • The Find Sequence output
• Collect Paired Read Statistics
  • How to run the Collect Paired Read Statistics tool
  • How to use the Collect Paired Read Statistics tool
• Reassemble Regions
  • How to run Reassemble Regions
• Extend Contigs
  • How to run Extend Contigs
• Join Contigs
  • How to run the Join Contigs tool
• Remove Extension of Contigs
  • How to run the Remove Extension of Contigs tool
• Annotate from Reference
  • How to run the Annotate from Reference tool
• Legacy tools and template workflows
  • Correct PacBio Reads
    • How to run the Correct PacBio Reads tool
    • Error-correction report
  • De Novo Assemble PacBio Reads
    • How to run the De Novo Assemble PacBio Reads tool
    • De Novo Assemble PacBio Reads report
  • PacBio De Novo Assembly Pipeline
• Bibliography

How to use the Analyze Contigs tool

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Subsections

• The contig analysis table
• How to edit data following contig analysis

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