Fertility testing

WES provides valuable information concerning family planning with the identification in healthy individuals of clinically relevant genetic variants that are associated with being a carrier of monogenic diseases, providing actionable choices for the health of their offspring.
In addition, WES can identify the genetic aetiology of male/female infertility.

WES does not identify certain genetic variations as, CNVs or trinucleotide repeats, methylated regions, and/or large deletions/insertions.

Sensitivity: >98%
Average coverage: 100Χ