New lower prices for services effective September 1st 2017. Contact us at infoservices@genomequebec.com for more details.

SNP Discovery Services - Sanger Sequencing Services

The Innovation Centre offers a SNP Discovery service and a service of de novo sequencing of complete plasmids by primer walking.

Full SNP Discovery/Validation services by Next-Generation Sequencing (NGS) include:

More information can be found in the User Guide.

Full SNP discovery services include:

  • Designing and ordering primers to amplify target regions
  • PCR amplification of target regions from genomic DNA of test samples based on Sanger Sequencing
  • Sequencing of PCR products based on Sanger Sequencing.
  • Detection of variations in test samples or between test samples and a reference sequence
  • Preparation and transmission of a SNP report including several annotations on the variations.

More information can be found in the User Guide.

The de novo sequencing service includes:

  • Sanger sequencing with an entry primer
  • Designing and ordering all primers needed to sequence the entire plasmid

More information can be found in the User Guide.