A test kit for whole exome and mitochondrial genome sequencing library preparation, compatible with next-generation sequencing (NGS) applications.
Professional Note
Please read the instructions for use (IFU) carefully before performing the test. Contact a Viet Huy technical specialist for on-site validation support in your laboratory.
Whole exome sequencing (WES) is a high-throughput next-generation sequencing (NGS) technique designed to capture and sequence the exon regions (protein-coding regions) of the human genome. WES enables the analysis of a large number of DNA fragments and provides the sequence of the entire coding region of an individual's genome, covering approximately 20,000 genes, thereby enabling detailed analysis of potential genetic factors associated with disease conditions. Although the coding region accounts for only 1% of the total genome, an estimated 85% of disease-causing mutations are located in this region.
Contact the Viet Huy technical team for more information.
| CE-IVD certified under EU Regulation 2017/746 (IVDR). | |
| Granted a marketing authorization (GPLH) by the Ministry of Health (MOH), classified as Class C | |
| Capable of sequencing approximately 42 Mb of the human exome (covering 19,441 genes), including the mitochondrial genome. | |
| Variants detected by the kit | CNV, InDel, SNP and SNV. |
| The procedure has been validated on DNA samples extracted from whole blood. | |
| Requires 10 ng to 500 ng of extracted DNA. | |
| The product has been validated on Illumina sequencing systems: NovaSeq 6000 and NextSeq 500/550. | |
| The included processing software has integrated AI | |
Coming soon
