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High-throughput Single-nucleotide Polymorphism (SNP) Genotyping for Biomarker Discovery

All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

There is an urgent need for new genetic biomarkers which enable the selection of optimal drugs. Single nucleotide polymorphisms (SNP) are known to affect the outcome of anticancer drugs used in the management of cancers. They may be used as noninvasive prognostic and predictive biomarkers to guide personalized treatment decisions. Creative Biolabs is well equipped and versed in high-throughput SNP genotyping for Biomarker Discovery. We are glad to serve our global clients with professionalism and expertise in SNP genotyping.

SNP: Potential Prognostic and Predictive Biomarkers

SNPs are the most frequently occurring genetic variation in the DNA sequence. They involve a single base and have a frequency of greater than 1% in at least one minor allele population. The total number of SNPs in the human genome exceeding 9 million. They are important biomarkers in many studies that link sequence variations to phenotypic changes, elucidating the molecular bases of diseases. Certain SNPs have already been identified as potential predictors of efficacy and/or toxicity in renal cell carcinoma (RCC) patients treated with tyrosine kinase inhibitors. Moreover, SNPs prove to be important determinants in evaluating and predicting a patient's response and to treatment and risk of adverse events.

High-throughput Single-nucleotide Polymorphism (SNP) Genotyping for Biomarker Discovery

High-throughput SNP Genotyping for Biomarker Discovery at Creative Biolabs

Over the past few years, Creative Biolabs has devoted a great deal of effort to developing accurate, rapid, and cost-effective technologies for SNP analysis. Our scientists have developed several SNP genotyping technologies, depending on the species, the number of SNPs per sample, applications, and purpose, as follows.

  • Genome-wide SNP genotyping by next-generation sequencing (NGS)
  • Gene-wide SNP genotyping by array-based technologies or NGS
  • Individual SNP analysis by real-time PCR, Sanger sequencing or NGS

High-throughput Single-nucleotide Polymorphism (SNP) Genotyping for Biomarker Discovery

For SNP genotyping by NGS, scientists at Creative Biolabs are proficient at retrieving information related to the genes identified in the common and rare variant analysis for biomarker discovery. Common SNP association analysis is performed using univariable and multivariable logistic regression while rare-variant association analysis is performed using a multi-marker test.

Highlights of Our High-throughput SNP Genotyping Service

  • Common SNP analysis
  • Rare SNP analysis
  • Genomic selection
  • Targeted genotyping by sequencing of (100-10000) markers
  • De-novo variant detection in target SNP region
  • High-throughput processing

With proven experience in SNP genotyping for biomarker discovery, Creative Biolabs is an ideal company to entrust with your business. Our comprehensive portfolio provides reliable and accurate SNP analysis to help our clients' genetic biomarker development project. For more information, please feel free to contact us and further discuss with our scientists.

Reference

  1. Garrigós, C.; et al. Single nucleotide polymorphisms as prognostic and predictive biomarkers in renal cell carcinoma. Oncotarget. 2017, 8(63):106551.
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