SANGER SEQUENCING, SINGLE VARIANT

This test is useful for validation of the reported variants where testing is performed using NGS technology for the proband and all the additional family members. In addition sanger sequencing can be performed for all the major hotspots, SNPs or any rare variant within human genome.

  • Test Type:
  • Pre-test Information:
    Clinical history in Test Requisition Form – Nx Gen Clinical Exome Sequencing & Reflex confirmation with Sanger Sequencing (Form 38) is mandatory.
  • Report Delivery:
    Sample Daily by 9 am; Report 30 days
  • Components:
    0