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Detect Structural Variants At 1% Allele Fraction Dive deeper into heterogeneous cancer samples Learn More
Detect Structural Variants At 1% Allele Fraction Dive deeper into heterogeneous cancer samples Learn More
Detect all structural variants genome-wide From 500 bp to aneuploidies, with sensitivity up to 99% Learn More
Detect all structural variants genome-wide From 500 bp to aneuploidies, with sensitivity up to 99% Learn More
Saphyr: Replace karyotyping, FISH and array with Learn More
Saphyr: Replace karyotyping, FISH and array with Learn More
Assemble error-free genomes Scaffold sequence contigs to build reference quality genomes Learn More
Assemble error-free genomes Scaffold sequence contigs to build reference quality genomes Learn More
Get Bionano Data Choose from three genome imaging Learn More
Get Bionano Data Choose from three genome imaging Learn More
Resolving Complex Haplotypes Implicated in Alzheimer’s and Other Neurodegenerative Diseases
Mayo Clinic
Dr. Mark T. W. Ebbert
August 26, 2020, 8:00A PDT | 11:00A EDT | 5:00P CET
View Webinar Next Generation Cytogenetics: Genome imaging for comprehensive germline and somatic structural variant detection
Radboud Medical Center, Nijmegen, The Netherlands
Alexander Hoischen, PhD
View Webinar From Data to Discovery: Tools to identify the pathogenic structural variant in patients with genetic disease
Children's National Medical Center
Dr. Hayk Barseghyan
View Webinar
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