If the Reference Sequence screen appears, you must input some type of reference sequence or genome template package before proceeding further in the wizard.

If you are following one of the Genome finishing workflows, this screen is called Input Draft Genome or Contigs or Input High Quality Draft Genome. These screens each contain a subset of the options in the Reference Sequence screen.

Optional pre-import steps for the Reference Sequence screen:

Add and remove reference sequence files or draft genomes:

SeqMan NGen can read and produce output using a variety of common chromosome naming conventions, including “chr1” and “ch1,” as well as Arabic and Roman numerals. See our Supported File Types page for allowable file extensions.

Options pertaining only to the Reference Sequence screen:

Click Next > to proceed to the next wizard screen or < Back to return to the previous screen.

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