Bionano will be present in full force at the upcoming American Society of Human Genetics (ASHG) Annual Meeting, October 17 to 21 in Orlando, Florida. We have a brand new booth (#555), an exciting workshop, and over a dozen scientists are presenting data generated with Bionano – studies on a scale we haven’t seen before.
This year, we are presenting Saphyr, our most advanced system for genome mapping. Saphyr has roughly 10 times the throughput of its predecessor, allowing it to generate sufficient data in one day to map up to two human genomes. This increase in throughput enables larger scale studies like the ones presented at this conference.
You don’t want to miss our workshop on Friday. This year, it is led by prominent genomics researchers, Dr. Jim Broach from Penn State University, Dr. Vanessa Hayes from the Garvan Institute, and Dr. Hayk Barseghyan from Children’s National Medical Center. The discovery of structural variations using Bionano mapping in cancer and other genetic diseases will be presented:
Solved with Bionano: How Order and Orientation Help Understand Genetic Disease.
Oral Session 80: Next-Generation Mapping (NGM): A novel approach for genetic diagnosis of structural variants.
Oral Session 26: Single-molecule mapping of complex genomic regions across 26 human populations reveals population specific variation patterns.
Poster #1501/W: Comprehensive discovery of genomic variation from the integration of multiple sequencing and discovering technologies.
Poster #2293/W: De novo genomic assembly and assessment of inbreeding in a severe bottleneck population.
Poster #808/W: Optical mapping reveals a higher level of chained fusion events in human cancer.
Poster #946/W: Characterization of a complex translocation causing 3q28ter duplication and 10q26.2ter deletion in a child with self-injurious behavior.
Poster #1487/T: Disease Relevant Structural Variation Analysis by Bionano Mapping.
Poster #806/T: An integrative detection and analysis of structural variation in cancer genomes.
Poster #1520/T: Automation of Ultra-High Molecular Weight DNA Isolation and Labeling for Genome Mapping.
Poster #788/T: Use of Bionano Genome Maps to Identify Medically-Relevant Genomic Variation.
Poster #2582/T: Structural variant detection with optical mapping and microfluidic partitioning: A t(9;13) case report.
Poster #2526/F: Investigating complex structural variants using third generation genome sequencing and mapping technologies.
Poster #405/F: Revisiting the mouse reference genome: Single molecule sequencing of C57BL/6J “Eve”.
Poster #423/F: Updates to the human reference genome assembly (GRCh38).
Poster #1032/F: Combining Bionano and exome sequencing identifies a homozygous structural variation in the novel AGBL3 gene underlying microcephaly.
Poster #1332/F: An alignment-based approach for sensitively detecting SVs using optical maps data.
Come see us at booth 555 in the exhibit hall. We look forward to see you in Orlando!
