FinIS allows users to close gaps in the genome assembly as well as validate the genomic scaffold. It considers all gaps simultaneously to find gap sequences that best match the read data and to correctly resolve repeats. For further details see the FinIS webpage and the publication describing FinIS.

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  • cherylgardner Posted 2013-05-31
    5 out of 5 stars
    Easy for use.
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2012-06-28
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