v12.3 [Aug 12, 2015]
May include unspecified updates, enhancements, or bug fixes.
v12.2 [Mar 4, 2015]
- it improves the NGS alignment algorithm by incorporating the best practices in variant calling.
- This version also offers a web monitoring tool for DNASTAR Cloud Assemblies, adds support for metagenomic pair data, and adds the ability to utilize alternate genetic codes within our genome template packages. Earlier releases of version 12 included access to DNASTAR Cloud Assemblies, a new gene panels workflow, and unaligned BAM file support.
Creates a high number of bioinformatics analyses, with graphical shown results.
