The optical mapping approach from Bionano Genomics is unlike anything else. With this unique tool, their dynamic team is driving change and empowering discovery across all areas of genome research. The Bionano solution resolves large scale structural variations missed by Next Generation Sequencing.
. 99% sensitivity for homozygous insertions/deletions larger than 500 base pairs
. 95% sensitivity for heterozygous insertions/deletions larger than 500 base pairs
. 95% sensitivity for balanced and unbalanced translocations larger than 50,000 base pairs.
. 99% sensitivity for inversions larger than 30,000 base pairs
. 97% sensitivity for duplications larger than 30,000 base pairs
. 97% sensitivity for copy number variants larger than 500,000 base pairs
Sample preparation, DNA imaging and genomic data analysis technologies
Bionano offers sample preparation, DNA imaging and genomic data analysis technologies combined into one streamlined workflow that enables you to identify structural variants and create de novo genome assemblies like never before.
Saphyr®, Bionano’s third-generation optical mapping solution, provides what’s missing in genome research – rapid, high-throughput, long-range genome mapping with unmatched structural variation discovery capabilities.
Bionano Access is a web based hub providing all the sofware required for Bionano genome mapping. Access allows users to setup runs, start de novo assemblies and strucutral variation analysis, visualise and manipulate maps and analyse trio’s.