GENOMIC SERVICES
OVERVIEW
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
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.
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
Quality
Retrogen utilized industry standard reagents and workflows to provide accurate and reproducible results
Difficult Templates
Proprietary workflows enable sequencing the most difficult templates
Quick Turnaround time
Starting from Next-day
Support
Experienced technical support to design, execute and help analyze your experiments
Support
Experienced technical support to design, execute and help analyze your experiments
Online
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.
![contact](https://retrogen.net/wp-content/uploads/2019/10/contact.png")
