Welcome to AThenaAI

Our advanced variant prioritization process uses a combination of bioinformatics tools and clinical guidelines to identify the most clinically relevant variants from genomic data. This helps researchers and clinicians to focus on the most promising variants for further investigation and interpretation.

With our sophisticated algorithm, we ensure that the biologically meaningful information is extracted from the processed data. This way, our customers can make more informed decisions and accelerate their research or diagnostic workflows.

With high performance infrastructure, a quality control, read alignment, and variant calling are performed in a timely manner. The raw sequence reads are checked for quality, aligned to a reference genome, and variants (such as SNP, insertions, or deletions) are identified.

Our polygenic risk score test is a powerful tool that utilizes genetic data to predict an individual's risk for developing certain diseases.

With our advanced platform, we can provide personalized healthcare services that allow patients to take proactive steps to prevent or manage health issues. Our test offers high accuracy and reliability, and highly adaptable and can be customized to meet the specific needs of each patient.