Description: NGS has reached an efficiency plateau with its flat flow cells. Single Technologies introduces 3-D Sequencing™, with a revolutionary three-dimensional sample platform that significantly increases the number of DNA sequences read in parallel. 3-D Sequencing™ seamlessly integrates sequencing with spatial biology, offering unprecedented insights and capabilities. It not only enhances sequencing efficiency but also provides a deeper understanding of biological structures and functions.
dna (838) life-science (311) ngs (136) sequencing (57) next-gen sequencing (8)
Company Careers Contact Adding a New Dimension to DNA Sequencing Pioneering 3-D Sequencing™ Single Technologies’s unique 3-D Sequencing™ technology allows us to read DNA in volumes, which drastically increases the number of DNA sequences that can be read in parallel and naturally bridges Next Generation Sequencing with Spatial Biology
To Sequence Everyone Identification of rare disease Whole-genome sequencing for rare diseases has the power to help doctors diagnose genetic diseases quickly, helping families avoid long diagnostic odysseys. Roughly 8% of the population is expected to have a rare disease. Around 80% of rare diseases are of genetic origin and, of those, 70% appear already in childhood.
To Sequence Everything DNA-labelled barcodes A probe in molecular biology is often a single-stranded sequence of DNA used to search for its complementary DNA or RNA sequence in a sample genome or an antibody used to identify the presence of a specific protein. All probes could use an attached barcode tag with nucleotides that could be detected with sequencing. There is a strong demand to detect many more probes in parallel in multiomics or in search of disease specific biomarkers.