SwiftSeq can perform variant calling on exomes in minutes and genomes in hours.
Align, clean, and variant call DNA sequencing data using clusters, clouds, supercomputers, or even your desktop.
SwiftSeq was designed knowing bioinformatics tools and computation resources are not static.
Algorithms and their parameters can be specified using a simple JSON configuration file.
Designed for flexibility and modularity, our web app allows you to intuitively generate your workflow while maintaining the customizability that you need. Workflows are output as a small and sharable JSON file. Simply feed your data and this configuration into SwiftSeq and get back to doing science.