We’re on a mission to transform the way the world sees the genome. By combining the best-in-class analysis software of BioDiscovery with the structural variant detection power of optical genome mapping, we’re equipping cancer researchers with better tools, expanded services and an expert team. Let’s solve the complexities of cancer together to elevate the health and wellness of all people.
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- AACR 2022

One Team. More Solutions.
Working together to reveal more genomic variations that matter in cancer research.
Explore Our Solutions at Booth #4021.
One company working together to transform the way the world sees the genome.
FINDING COMMUNITY AND CONNECTION AT AACR

As part of our mission to elevate the health and wellness of all people, Bionano Genomics takes the fight against cancer personally. We’re committed to playing an important role in service to the cancer research community — building better tools, asking harder questions, and working together to make genomic discoveries that can ultimately lead to better outcomes for people diagnosed with cancer.
Decoding Cancer Complexity
View and analyze detected genomic scars associated with HRD in NxClinical, the leading copy number variation (CNV) analysis software solution for cytogenetics and molecular laboratories.
The latest NxClinical software (v6.2) release calculates three measures of genomic instability for homologous recombination repair deficiency (HRD) in solid tumors, from NGS and CMA data.
- Loss of Heterozygosity (LOH)
- Telomeric Allelic Imbalance (TAI)
- Large-Scale State Transitions (LST)
Join us in the Exhibitor Spotlight Theater
Experts will showcase this new capability of NxClinical™ software:
Application of Optical Genome Mapping for Comprehensive Genomic Structural Variation and HRD Analysis from Tumor Biopsies
Dr. Ravindra Kolhe* and
Dr. Miriam Bornhorst**
**Children’s National Hospital
Engage with two poster presentations showing results from OGM applications.
Learn more about how these teams are using OGM in their cancer research at their poster presentations.
Poster 2931: Optical genome mapping workflow for identification and annotation of variants in hematological malignancies
Authors: Jennifer Hauenstein, Andy Pang, Alka Chaubey, Alex Hastie
Presented: April 12, 2022, 1:30 – 5:00 PM
Poster 2933: Utility of optical genome mapping for the chromosomal characterization of cell lines used in preclinical and clinical research
Authors: Nikhil S. Sahajpal, Ashis K. Mondal, Alex Hastie, Alka Chaubey, Ravindra Kolhe
Presented: April 12, 2022, 1:30 – 5:00 PM
(click on poster # above to view pdf)