svim

Structural variant caller for long sequencing reads

Description

SVIM is a structural variant caller for long sequencing reads. It is able to detect, classify and genotype five different classes of structural variants. Unlike existing methods, SVIM integrates information from across the genome to precisely distinguish similar events, such as tandem and interspersed duplications and simple insertions.

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Homepage

https://github.com/eldariont/svim


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