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Enabling Next-Generation Cytogenetics with Optical Mapping - Applications in Medical Genetics

3 Jul 2019
Enabling Next-Generation Cytogenetics with Optical Mapping - Applications in Medical Genetics

Structural variants (SVs) represent an important source of genetic variation in the human genome and are involved in a multitude of diseases, such as cancer and developmental disorders. In this presentation at the European Society of Human Genetics (ESHG) conference 2019, Dr. Alexander Hoischen, Associate Professor, Immuno-Genomics Radboud University Medical Center, discusses SV detection using optical mapping technology and the new Saphyr system from Bionano Genomics. Supported by data presented in this talk, Hoischen hypothesizes that optical mapping technology may largely replace classical cytogenetic tests in the future.

Saphyr Chip®

Bionano Genomics

The Bionano Saphyr Chip ® utilizes hundreds of thousands of massively parallel NanoChannels that linearize long DNA molecules allowing Bionano systems to directly image your samples.

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Saphyr® System

Bionano Genomics

Saphyr, Bionano’s high-speed, high-throughput genome mapping solution, detects and analyzes genome-wide structural variations with exceptional sensitivity and specificity to reveal the true structure of any genome. Saphyr’s breakthrough speed and throughput combined with unmatched structural variation sensitivity make it the ideal solution for identifying disease-associated structural variants in human genetics and oncology translational and clinical research studies.

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Enabling Next-Generation Cytogenetics with Optical Mapping - Applications in Medical Genetics