Detect chromosomal 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.
See our range of cfDNA products below.
Cell3™ Target: ExomeCG – Cytogenetics Exome
An exome enrichment specifically for cytogenetic analysis that lets you detect all variants (SNVs, indels and CNVs) in a single assay from as little as 10ng input. Suitable for constitutional postnatal and prenatal analysis.
Less handling. Less time. More results first time.
Cell3™ Target: Carrier Screening Panel
A comprehensive panel covering variants for 488 severe recessive childhood disorders in one NGS workflow. No arrays. No MLPA.