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.
Follow FinIS
Other Useful Business Software
AI-powered service management for IT and enterprise teams
Give your IT, operations, and business teams the ability to deliver exceptional services—without the complexity. Maximize operational efficiency with refreshingly simple, AI-powered Freshservice.
Rate This Project
Login To Rate This Project
User Reviews
-
Easy for use.