SMALT aligns DNA sequencing reads with a reference genome.
Reads from a wide range of sequencing platforms can be processed, for example Illumina, Roche-454, Ion Torrent, PacBio or ABI-Sanger. Paired reads are supported. There is no support for SOLiD reads.
InstallationUse the following command to install this title with the CLI client:
$ biogrids-cli install smaltAvailable operating systems: Linux 64, OS X INTEL
Linux 64:  0.7.6 (2.7 MB)
OS X INTEL:  0.7.6 (898.3 KB)