Single nucleotide variant validation
We validate any SNVs identified through exome, whole genome or targeted sequencing.
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To validate any SNVs identified through exome, whole genome or targeted sequencing.
The SNV Validation services we provide:
- Validation using fluorescence-based KASP assays (LGC Genomics). Primers are designed using a semi-automated pipeline and results are provided in excel format.
- Option to request Sanger sequencing assay to be designed to the SNV if a KASP assay fails to design.