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Single cell capture platform
Microarray platform
NGS platform

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PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

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Endometrial receptivity assessment
Circulating tumor cell capture

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Clinic test

Home Clinical detection CNV-seq Testing Content

CNV-seq

Column List

PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

• Chromosomal aneuploidy
• Over 1MB chromosome copy number deletion and duplication
• A certain proportion of chimeras

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4008-213-671

infor@unimeddx.com

www.unimeddx.com

Introduction
Expert team
Certificates

Single cell capture platform
Microarray platform
NGS platform

PGT-M/PGT-SR
PGT-A
Prenatal genetic diagnosis
cb-NIPT
Noninvasive prenatal paternity test
Neonatal genetic disease screening
Genetic analysis of misarriages
Genetic screening
Fragile X syndrome screening
AZF microdeletion and sex chromosome aneuploidy screening
Clinical whole exome sequencing
CNV-seq

Endometrial receptivity assessment
Circulating tumor cell capture

Company news
Marketing activities
Science news
Documents

About Unimed
Managemet team
Partners
Recruitment
Contact us

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