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{{Bioinformatics application
|sw summary=De novo and reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD data. Support for paired and single reads. Alignment in base- and color-space, and mixed mode. Support for paired of any of the above including both short and single long reads. Includes tools for SNP and small indel detection and annotation. Runs equally well on Windows, Mac OS X and Linuxplatforms, plus server/enterprise options for scalability of computation and storage.
|bio domain=Genomics, Whole Genome Resequencing, De-novo assembly, SNP discovery, InDel discovery, ChIP-Seq, RNA-Seq and much more...
|bio method=Mapping, Assembly, and Alignments, accelerated with SIMD implementation and multi-threading.Package includes many more common-place bioinformatics tools such as BLAST, wrappers, genetic variation annotation, Statistics, Visualisation,and Clustal alignments as well.
|bio tech=454, Illumina, ABI Solid, Helicos, Sanger,
|created by=Thomas Knudsen and Bjarne Knudsen et al
