The POLARIS Clinical Exome Test (CET) is a high-throughput sequencing assay that analyzes the coding portion of >19,000 genes in the human genome. It has been validated to provide a comprehensive coverage of >19,000 Refseq genes with an average sequencing depth of > 100x, and can detect single nuclear variations (SNVs), and short insertions and deletions (indels, up to 10bp).
The CET is validated according to CAP guidelines for extracted DNA samples, and sequencing files and a technical report are provided. It is intended to assist in the diagnosis of the genetic basis of rare disorders by a physician.
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