At Dhiti Omics, state-of-the-art technologies are incorporated in all workflows for

Depending on the requirement of the assay, Sanger sequencing, Next-Generation Sequencing or Microarray platforms are employed. Sanger sequencing is the gold standard for validation of short listed variants. Next Generation Sequencing involves massively parallel sequencing and enables the sequencing of several loci at a time. 

Microarray technology is useful for the detection of large chromosomal aberrations such as copy number variations. Appropriate analytical pipelines are used for data storage, analysis and reporting and ensure confidentiality of the process.