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WES+CNV-seq CapitalBio

Combination of individual WES + CNV-seq, detect single-gene disorders and chromosomal diseases, comprehensively investigate the causes of children's intellectual disability, developmental delay, repeated miscarriage and infertility.

whole exome sequencing genetic test

Clinical Applications of WES+CNV-seq

  • Pediatrics: patients with atypical disease characteristics, unexplained developmental delay and intellectual disability, probands with malformations and their parents.

  • Obstetrics: couples with recurrent miscarriage (including stillbirths) or abnormal pregnancy.


  • High-risk populations requiring clarification of the cause of genetic diseases.

  • Patients with undiagnosed causes by other medical tests.


Specification

Sample typesWhole blood / Tissue / Blood spot card
TAT20 working days


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86-10-69002900
Building C, Block 88 Kechuang 6th Street, Yizhuang Biomedical Park, Beijing