Yikon Genomics

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Yikon Genomics, founded in 2012 and based in Shanghai and Suzhou, is dedicated to advancing reproductive health and personalized cancer genetic services. We operate a medical laboratory in Suzhou and have offices in Hong Kong, Spain, and Malaysia, making high-quality genetic services accessible globally. Our mission, "Innovate for the Health of Billions," drives our work in single-cell whole genome amplification and sequencing technology. Leveraging AI and machine learning, we offer decentralized and cost-effective genetic testing solutions for reproductive challenges and genetic risks. We innovate continuously, with key advancements including NICS (niPGT-A) and the first NICS baby in 2016, and the development of ERT in 2018, supporting families worldwide in achieving healthy live births. Our strengths lie in our continuous innovation, rigorous clinical validation (including IVD applications and RCTs), strong execution, and ability to translate scientific research into clinical applications. These strengths result in decentralized, cost-effective, and rapid turnaround genetic services. With a presence in over 600 medical institutions, including more than 200 reproductive centers across 40+ countries, our vision is to help 100 million families improve their health and become the leading brand in precision medicine, supporting successful treatment outcomes with sustainable practices.

Company Details

Employees
46
Founded
-
Address
Xuhui District, Shanghai,china
Phone
0086-400-9123-918
Email
nf****@****ics.com
Industry
Biotechnology Research
NAICS
Research and Development in Biotechnology (except Nanobiotechnology)
HQ
Shanghai
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Clinical outcomes of frozen-thawed blastocysts with twice noninvasive chromosome screenings (NICS) - Frontiers

Clinical outcomes of frozen-thawed blastocysts with twice noninvasive chromosome screenings (NICS) Frontiers

Dx&Vx introduces Yikon Genomics technology to enhance infertility diagnostics - koreabiomed.com

Dx&Vx introduces Yikon Genomics technology to enhance infertility diagnostics koreabiomed.com

Nanopore sequencing with T2T-CHM13 for accurate detection and preventing the transmission of structural rearrangements in highly repetitive heterochromatin regions in human embryos - Wiley Online Library

Nanopore sequencing with T2T-CHM13 for accurate detection and preventing the transmission of structural rearrangements in highly repetitive heterochromatin regions in human embryos Wiley Online Library

Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media - Frontiers

Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media Frontiers

Genetic risk stratification and risk factors of early menopause in women: a multi-center study utilizing polygenic risk scores - Frontiers

Genetic risk stratification and risk factors of early menopause in women: a multi-center study utilizing polygenic risk scores Frontiers

Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1 - Frontiers

Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1 Frontiers

A Rapid NGS-Based Preimplantation Genetic Testing for Chromosomal Abnormalities in Day-3 Blastomere Biopsy Allows Embryo Transfer Within the Same Treatment Cycle - Frontiers

A Rapid NGS-Based Preimplantation Genetic Testing for Chromosomal Abnormalities in Day-3 Blastomere Biopsy Allows Embryo Transfer Within the Same Treatment Cycle Frontiers

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