Moving Us Forward
We look forward to connecting with you in Boston for the American Society of Human Genetics (ASHG) conference from October 14-18, 2025. ASHG will cover a broad spectrum of topics including new technologies, applications, and research to showcase the most compelling genetics and genomics science of the year. For more details on Bionano and OGM-related activities, please see below.
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Connect
At Booth #2178
Learn
Platform & Poster Sessions
Booth #2178
Visit us at booth #2178 to meet with our OGM specialists to learn how your current workflow can be elevated with Bionano’s end-to-end OGM solutions. Plus, get the latest on our Stratys™ system, and VIA analysis software.
Learn
Discover the latest advances in OGM at ASHG! Visit our posters and platform sessions to explore how Bionano technology is driving innovation in rare disease, oncology, and prenatal genetics. From improved algorithms and precision diagnostics to real-world applications, our experts and collaborators will showcase groundbreaking research throughout the week.
| POSTER | TITLE | LEAD AUTHOR |
|---|---|---|
| Board 4012W | Improved algorithms for optical genome mapping workflows in constitutional disease and oncology applications |
Andy Wing Chun Pang
Bionano Genomics |
| Board 8020F | Precision Diagnosis of FSHD1 via Optical Genome Mapping: Efficient Detection and Characterization |
Trilochan Sahoo
Bionano Laboratories |
| Board 8030W | Optical Genome Mapping and Long Read Sequencing Identifies a Novel 27kb Dystrophin Gene Inversion in a Patient with Duchenne’s Muscular Dystrophy |
Ulrich Broeckel
Medical College of Wisconsin |
| Board 4018W | Project Baby Magnolia: Implementing Optical Genome Mapping in a Genomic Medicine Program at the University of Mississippi Medical Center |
Douglas McLaurin
University of Mississippi Medical Center |
| Board 8027T | Comparison of optical genome mapping, chromosomal microarray and next generation sequencing analyses for detection of structural variants in rare diseases |
Kumiko Yanagi
National Center for Child Health and Development |
| Board 9074T | Optical genome mapping elucidates complex structural variants caused by germline chronotropisms in a patient with developmental delay |
Masanori Fujimoto
Nagoya City University Graduate School of Medical Sciences |
Platform Session
Completely resolved structural variants by optical genome mapping with adaptive sampling from CNV discovery
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Wednesday, October 15, 2025
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1:45 PM – 2:00 PM
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Location: Room 258ABC/Level 2
Part of Session 27: Advanced Technologies Uncover Dosage, Structure, and Phenotypic Complexity 01:30 PM – 02:30 PM
Li Fu
Yokohama City University Graduate School of Medicine
Platform Session
Prospective comparative evaluation of optical genome mapping, mate-pair genome sequencing, and chromosomal microarray analysis in prenatal genetic analysis of fetuses with ultrasound anomalies
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Saturday, October 18, 2025
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9:00 AM – 9:15 AM
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Room 206AB/Level 2
Part of Session 87: Prenatal Genetics and Reproductive Health 08:30 AM – 09:30 AM
