We are moving towards the sophisticated and continuously developing world of information technology. Computer power comes into play when researchers in the genomics field are dealing with huge amount of data, for example, the human genome, which comprises of 6 billion base pairs. To be able to sequence, align, analyze and interpret this overwhelmingly large amount of data is absolutely crucial for scientists looking to achieve their research goals in a shorter period of time, yet with high accuracy and effectiveness. These data are known as next-generation sequencing (NGS) data.
Market’s leading aligner with fully packed features designed for mapping of short reads onto a reference genome from Illumina, Ion Torrent, 454, and Color Spance NGS platforms.
Leading aligner packed with features designed to fully support reads from ABI SOLiD Color Space.
Custom designed multi-threaded sort/merge tools for BAM files.
Our mRNA aligner suitable for reads from Illumina, PacBio, BGI and Nanopore sequencers.
User-friendly, easy to setup, and powerful workbench for analysis of Exome, RNA, MiRNA, Whole Genome, Basic NGS Alignment, and etc. Highly customizable and fine tune-able to cater to your research needs.
A patient-centric NGS sequence analysis platform and reporting system for wellness and clinical reporting based on NovoWORX workflow system. Easily customisable using multiple annotation databses, a rule based variant ranking & selection with a template driven reporting system.