Changes

|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 assemblywhich reduces sequencing errors. Requires Win or MacOS.|bio domain=Sequence assembly (de novo assembly), Metagenomics, SNP detection, Indel detection, Exome capture, |bio tech=Illumina, 454, ABI SOLiD|created at=SoftGenetics LLC|maintained=Yes|input format=FASTQ, FASTA, Scarf, FNAQual, CSFASTA/CSQUAL (ABI SOLiD),|sw feature=Unique condensation tool, Data Visualisation, very flexible|language=C++,|licence=Commercial|os=Windows