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Sanger Sequencing

Sanger sequencing is widely used to get high quality long read (up to 500 bp or more) targeting smaller genomic regions in a larger number of samples. 

BioXplore offers a wide range of services for Sanger Sequencing to match your project needs.

  • Sequencing PCR products and plasmid sequences, inserts, mutations.
  • Sequencing of variable regions
  • Validating results from next-generation sequencing (NGS) studies
  • HLA typing
  • Genotyping of microsatellite markers
  • Identifying single disease-causing genetic variant