Our OGM systems, software solutions and uncompromising support allow you to reveal more genomic variation that matters across a variety of applications in clinical care, research and therapeutics.
Solve the complex biology of hematological malignancies and solid tumors by revealing structural variants traditional methods miss and create new opportunities for personalized care.
Learn MoreSee chromosomal aberrations with digital clarity and deliver new answers for reproductive health issues, neurodevelopmental delay and rare disease.
Learn MoreEnhance your quality control and ensure the genomic integrity and stability of cell lines for producer cell lines, research cell lines and cell therapy applications.
Learn MoreTransform your laboratory workflow and detect all classes of chromosomal aberrations in cancer and genetic disease cases with digital precision.
Learn MoreAchieve more comprehensive structural variant profiles than sequencing alone provides and maximize pathogenic findings in your cancer and genetic disease cases.
Learn MoreJoin the growing community of Bionano users worldwide who are moving healthcare and hope forward with our solutions. Watch their stories and learn how Bionano OGM systems and software solutions can help you break through.
The Saphyr system provides genome-wide detection and analysis of all classes of structural variants from ultra-high molecular weight DNA using OGM.
Learn MoreBionano NxClinical is a platform-agnostic analysis software solution that provides comprehensive analysis and interpretation of genomic variants from miroarray and NGS data in one view.
Learn MoreLet's Move Forward Together! Join us in Orlando, Florida, USA, for the American Association for Cancer Research annual meeting. Together, we can reveal more variation that matters in cancer research. Exhibits open on Friday, April 14, 2023 - Visit the Bionano team in booth #1319.
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