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

Mutation analysis

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

SNP Genotyping

Profile your sample with a fixed-panel or we can help you develop a custom panel covering just your regions of interest.

Sequence verification

Sanger sequencing is a common downstream verification step for many mutation detection assays. Send submit your samples for verification today!

Fragment Analysis

RFLP, ITDs, microsatellites, many biomarkers can be detected via capillary electrophoresis.

Features & Benefits


Retrogen utilized industry standard reagents and workflows to provide accurate and reproducible results

Difficult Templates

Proprietary workflows enable sequencing the most difficult templates


Local pickup available in select areas

Quick Turnaround time

Starting from next – day


Experienced technical support to design, execute and help analyze your experiments


Online customer portal for placing orders and retrieving data

How to Order

Refer to the sample submission guidelines for your application
Once your samples are ready, login to place your order, or call customer support.