728
edits
Changes
no edit summary
{{Bioinformatics application
|sw summary=de novo and reference assembly of Roche/454, Illumina and SOLiD data. Uses a novel Condensation Assembly Tool approach where reads are joined via "anchors" into mini-contigs before assembly which reduces sequencing errors. Requires Win or MacOS.
|bio domain=SNP/Indel Detection, De novo sequencing, targeted resequencing and transcriptome sequencing, Metagenomics, SNP discovery, InDel discovery,
|bio tech=Illumina, 454, ABI SOLiD
|created at=SoftGenetics LLC
