Customized Genomics Solutions
At Advait Theragnostics, we specialize in partnering with clients to develop custom genomics workflows tailored to specific research goals and experimental requirements, ensuring that each solution is precisely aligned with their unique needs. Whether you require comprehensive whole genome analysis to uncover insights, the identification or quantification of specific genetic variants for targeted studies, or seamless integration with other omics data to achieve a multidimensional understanding, our dedicated team brings expertise and innovation to every project. With a focus on expediting and enhancing the outcomes of your research, we are committed to delivering solutions that drive meaningful progress and empower scientific discovery.
Unlocking the Power of DNA Analysis
Discover the power of genomics with our comprehensive suite of services tailored to meet your research needs. At Advait Theragnostics, we offer cutting-edge genomics solutions like mutation screening and detection, SNP genotyping and a range of other high-impact genomic investigations. Our experienced team is committed to delivering accurate, timely and insightful genomic data to empower your scientific endeavours. Whether you are in academia, biopharma, clinical diagnostics, veterinary science or microbiology, explore how our genomics services can accelerate your projects.
Mutaition Screening
Our mutation screening services leverage advanced technologies to detect and characterize genetic mutations associated with specific conditions. We employ PCR assays as well as state-of-the-art sequencing techniques like Sanger and next-generation sequencing (NGS) to accurately profile mutations in specific genes, genomic regions or entire genome. Whether you require targeted mutation analysis or comprehensive whole-genome screening, you can trust our expert team to deliver actionable insights to meet your research goals.
SNP Genotyping
Our SNP genotyping services utilize diverse platforms such as microarrays, real-time PCR assays and sequencing methodologies to assess single nucleotide polymorphisms (SNPs) across the genome. By pinpointing variations in DNA sequences, we enable genotype-phenotype correlations, population studies, and personalized medicine approaches. Our high-throughput workflows ensure robust and reproducible results, assisting you to make informed decisions based on genomic data.
