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Closing gaps in Assembly Projects and Align to Reference documents.

You can access many tools for closing the gaps in genome sequencing projects. If you select reads, then right click you will see a context sensitive menu with the following tools:

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Not all tools are applicable or available in all editors. Plus some tools are only enabled when using paired end reads. Here's what's available in each editor.

Align to Reference editor

Reference Contig editor

De novo contig editor

Related Topics.

Align to Reference

Assembler

Importing Fastq data

Bowtie

Phrap