SNP Discovery Sequencing

SNPs (single nucleotide polymorphisms) occur every 100 to 300 bases along the human genome and account for about 90% of all genetic variations. SNPs could predispose people to disease or influence their response to a drug. GENEWIZ offers a complete package of SNP discovery sequencing services.

This service includes -

• Assay development, including amplicon selection and primer design
• Assay optimization and validation
• High throughput PCR amplification, purification and bi-directional DNA sequencing
• Automated and manual analysis of sequencing results for SNP identification

SNP discovery assays are designed by our PhD scientists using both commercial and proprietary software. All assays are optimized and validated before large-scale screenings. PCR reactions are prepared in a sterile environment. All SNPs are reported in a consolidated format that is customized to your specifications.

We are pleased to discuss your project, to order this service, please email dnaseq@genewiz.com with your project information. GENEWIZ Customer Support will contact you to discuss the project scope in detail, or call GENEWIZ technical support.