FEATURES

• No read length restriction
• Can detect most small indels in either single-end or paired-end data sets
• Has a strong capability to identify variants based on a relatively divergent reference genome
• Provides a user-friendly graphic interface
• Can be used to detect intraspecific polymorphisms (including SNPs and indels) based on a pairwise comparison of multiple whole genomes
• Employs a global heuristic searching approach to layout contigs based on one or more reference genomes
• Also provides a handful of bioinformatic tools for read simulation, mutation incorporation, format conversion, etc.

FOR MORE INFORMATION