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URL: http://www.sanger.ac.uk/resources/software/smalt/
Proper Citation: SMALT (RRID:SCR_005498)
Description: Software that aligns DNA sequencing reads with a reference genome. Reads from a wide range of sequencing platforms, for example Illumina, Roche-454, Ion Torrent, PacBio or ABI-Sanger, can be processed including paired reads.
Abbreviations: SMALT
Resource Type: software resource
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