Allow Retrogen to expand your research potential with a host of workflows to support your molecular genetics interests. From PCR and Sanger sequencing to NGS and qPCR, Retrogen has the tools and expertise to enable a wide range of experiments.
Sanger sequencing and qPCR are often used to confirm NGS results, fragment analysis can identify short tandem repeats, homopolymers and microsatellites, while NGS can be used to screen antibody heavy and light chain sequences, detect rare alleles and for SNP genotyping. Contact us today to get your molecular genetics project started on the right path
Types of Service
NGS, qPCR or Sanger Sequencing
Depending on the scope of your project, there are a number of ways to verify or discover variants in your templates
NGS or qPCR
Profile your sample with a fixed-panel or we can help you develop a custom panel covering just your regions of interest.
Sanger sequencing is a common downstream verification step for many mutation detection assays. Send submit your samples for verification today!
Features & Benefits
Proprietary workflows enable sequencing the most difficult templates
Local pickup available in select areas