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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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Connect your AI agents to apps and data more securely, give users control over the actions AI agents can perform and the data they can access, and enable human confirmation for critical agent actions.
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