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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.
Your Benefits Include
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Assay development, including amplicon selection and primer design
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Assay optimization and validation
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High throughput PCR amplification, purification and bi-directional DNA
sequencing
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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
mb@genewiz.com with your project information. GENEWIZ Customer Support
will contact you to discuss the project scope in detail,
or call GENEWIZ technical support.
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