Detect chromosal abnormalities including SNVs, indels and CNVs in a single test
Library prep solutions that allow you to consolidate workflows, save time and resources and still deliver comprehensive reports
Traditional methods for comprehensively assessing the chromosomal abnormalities associated with constitutional disorders have required laboratories to implement several workflows from FISH and karyotyping to MLPA and arrays.
That’s why Nonacus have developed library preparation solutions for Next Generation Sequencing (NGS) that offer you the chance to consolidate these worklows into a single assay. Combining the analysis of SNV’s, indels and CNV’s into a single assay, they enable you to save time and resoures and still deliver a comprehensive report on constitutional abnormalities from one workflow.