How it works
The Just DNA-Seq platform consists of OakVar (Open-source Genomic Variant Analysis Platform) modules, bioinformatics pipelines, and additional libraries. One can realign and annotate the genome of interest employing Just DNA-Seq tools to retrieve information about variants associated with age-related diseases or major life threatening risks and longevity-associated variants present in genome.
Just DNA-Seq is a set of open-source libraries and pipelines designed to help you with:
- realigning your raw genome reads and doing variant calling using the latest tools and Bioinformatic pipelines
- annotating your own genome using longevity OakVar plugin with:
- known longevity, cancer risks
- known drug interactions
- cardio hereditary diseases risks
- coronary artery disease risks variations
- getting a comprehensive and transparent open-source report, inclusive of all previously mentioned information as well as polygenic health risk predictions and personal recommendations related to longevity.