Single nucleotide variant validation


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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.

Updated:  21 September 2018/Responsible Officer:  Director/Page Contact:  Site manager