Our platform combines cutting-edge biotechnology with AI-powered analysis to provide comprehensive genetic insights without invasive procedures.
Detect chromosomal abnormalities without invasive procedures, improving embryo selection safety.
Identify specific genetic mutations associated with inherited disorders with high accuracy, non-invasively.
Evaluate genetic risk for common conditions like diabetes, heart disease, and more for lifelong health.
Empowering parents with deeper genetic insights before embryo analysis
Get a Couple Report on your shared risk of passing on inherited conditions, plus Individual Reports for each parent outlining their personal genetic risks.
Easily download your complete raw genome data for both parents and embryos—ready to review, share with your doctor, or explore on your own.
Our streamlined non-invasive embryo process makes genetic testing accessible, safe, and efficient
Patients provide saliva samples, while IVF clinics send embryo cfDNA (non-invasive, no cells removed from the embryo) to one of our certified Partner Genomic Labs.
Partner Labs securely upload the raw genetic data—embryo cfDNA and parental genomes through our platform for analysis.
Our team of genomics experts and AI algorithms perform a comprehensive review using advanced non-invasive methods.
Receive a full genetic report with validated insights, followed by a 30-minute consultation with a board-certified medical genetics specialist to discuss your results and next steps.
Independent expert analysis of your existing genomic data for greater confidence in embryo selection
Our independent analysis provides validation of initial findings and deeper insights into embryo genomic health.
Hear from clinics and individuals who have benefited from our non-invasive technology
"BHALESHA's non-invasive testing has revolutionized our approach to embryo selection. The accuracy and depth of the genetic insights have significantly improved our success rates while ensuring patient safety."
"The comprehensive reports and interactive visualizations make it easy to communicate complex genetic information to our patients. BHALESHA's non-invasive approach has become an essential part of our practice."