Easy to use, comprehensive analysis tools are available for data upload from various sources such as NGS machines or other sequencing platforms like Ion Torrent PGM/S5 sequencer etc., The GUI is easy-to follow but not intuitive enough sometimes which can make it difficult at first glance especially if one has little knowledge about genome assembly pipeline; more features could be added in future releases (e g de Novo Assembly tool). We have used this software mostly during our initial phase when we were using Illumina Hiseq 2000 machine with paired end read length up to 150bp where there was no need to do any reassembly due lack of complexity that required complex algorithms unlike here! This would help us save time while working directly towards mapping reads against human reference sequences without having to go through some intermediate steps after alignment.