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Oncode Scientific Sdn Bhd

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Oncode Scientific Sdn Bhd

Oncode Scientific Sdn Bhd
201501029484 (1154805-X)

Leading the Precision Medicine Revolution in Asia

Since 2015, Oncode Scientific Sdn Bhd has emerged as a trailblazer in the realm of precision medicine, setting new benchmarks in cancer molecular diagnostics. Our multidisciplinary team, comprising top-tier experts from molecular science and clinical practice, brings together decades of experience in medical diagnostics and research. At our cutting-edge facilities in Malaysia, we spearhead one of Asia’s most pioneering precision medicine initiatives, specializing in both solid tumors and hematologic cancers. Our relentless pursuit of innovation drives us to constantly challenge the status quo, exceeding clinical and diagnostic standards to deliver groundbreaking medical solutions. Oncode is dedicated to transforming healthcare—advancing disease prevention, early detection, and targeted intervention. With a commitment to excellence, we provide world-class molecular diagnostic services that are both accessible and revolutionary, empowering the global community to embrace the full potential of precision medicine.

18/02/2026

May this season of reflection bring peace, balance, and well-being to you and your loved ones.

16/02/2026

🪭As the Year of the Horse begins, we wish you good health, steady energy, and days that feel balanced and positive.✨

May the year ahead unfold with peace of mind, renewed vitality, and meaningful moments shared with those who matter most.

14/02/2026

Oncode was honoured to participate in 𝗡𝗮𝘁𝗶𝗼𝗻𝗮𝗹 𝗥𝗮𝗿𝗲 𝗗𝗶𝘀𝗲𝗮𝘀𝗲 𝗗𝗮𝘆 𝟮𝟬𝟮𝟲 at Hospital Tunku Azizah, Kuala Lumpur on 4 February 2026.

The event also marked the 𝗹𝗮𝘂𝗻𝗰𝗵 𝗼𝗳 𝘁𝗵𝗲 𝗡𝗮𝘁𝗶𝗼𝗻𝗮𝗹 𝗣𝗼𝗹𝗶𝗰𝘆 𝗳𝗼𝗿 𝗥𝗮𝗿𝗲 𝗗𝗶𝘀𝗲𝗮𝘀𝗲𝘀 𝗶𝗻 𝗠𝗮𝗹𝗮𝘆𝘀𝗶𝗮 — a landmark step forward for the rare disease community, championing early diagnosis, affordable treatment, and integrated support.

Malaysia's public healthcare sector currently 𝘀𝘂𝗽𝗽𝗼𝗿𝘁𝘀 𝗼𝘃𝗲𝗿 𝟭𝟮,𝟬𝟬𝟬 𝗽𝗮𝘁𝗶𝗲𝗻𝘁𝘀 𝗮𝗰𝗿𝗼𝘀𝘀 𝗻𝗲𝗮𝗿𝗹𝘆 𝟱𝟬𝟬 𝗿𝗮𝗿𝗲 𝗱𝗶𝘀𝗲𝗮𝘀𝗲𝘀.

As Helen Keller said, “Alone we can do so little; together we can do so much”. Progress in rare disease care thrives when 𝗽𝗮𝘁𝗶𝗲𝗻𝘁𝘀, 𝗰𝗮𝗿𝗲𝗴𝗶𝘃𝗲𝗿𝘀, 𝗰𝗹𝗶𝗻𝗶𝗰𝗶𝗮𝗻𝘀, 𝗿𝗲𝘀𝗲𝗮𝗿𝗰𝗵𝗲𝗿𝘀, 𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗼𝗿𝗶𝗲𝘀, 𝗮𝗱𝘃𝗼𝗰𝗮𝗰𝘆 𝗴𝗿𝗼𝘂𝗽𝘀, 𝗮𝗻𝗱 𝗽𝗼𝗹𝗶𝗰𝘆𝗺𝗮𝗸𝗲𝗿𝘀 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗲, turning rarity into 𝗰𝗼𝗹𝗹𝗲𝗰𝘁𝗶𝘃𝗲 𝘀𝘁𝗿𝗲𝗻𝗴𝘁𝗵.

At Oncode, we are committed to 𝗽𝗿𝗼𝘃𝗶𝗱𝗶𝗻𝗴 𝗮𝗰𝗰𝗲𝘀𝘀𝗶𝗯𝗹𝗲 𝗮𝗻𝗱 𝗿𝗲𝗹𝗶𝗮𝗯𝗹𝗲 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗺𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗱𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰𝘀 that support early, accurate diagnoses — shortening years of uncertainty and guiding personalised care.

Together, we transform uncertainty into diagnosis, diagnosis into treatment, and treatment into hope.

13/02/2026

𝗨𝗻𝗶𝘁𝗲𝗱 𝗯𝘆 𝗨𝗻𝗶𝗾𝘂𝗲
More Than a Diagnosis. Every Story Matters.

As we look back at moments from past scientific meetings, collaborations, and shared milestones, we are reminded that progress in cancer care is built by people — researchers, clinicians, partners, and patients — each with a story that matters.

World Cancer Day’s 2025–2027 theme, “United by Unique,” reflects what we believe in: every cancer journey is different, and meaningful care begins with recognising individuality.

At Oncode Scientific, we remain committed to advancing precision diagnostics and personalised approaches — because no two patients, and no two cancers, are the same.

Together, we move from awareness to action.
Together, we are United by Unique.

23/01/2026

𝗜𝗻 𝗡𝗼𝘃𝗲𝗺𝗯𝗲𝗿 𝟮𝟬𝟮𝟱, Oncode proudly participated in the 𝗪𝗼𝗺𝗲𝗻’𝘀 𝗛𝗲𝗮𝗹𝘁𝗵 𝗖𝗼𝗻𝗳𝗲𝗿𝗲𝗻𝗰𝗲 𝟮𝟬𝟮𝟱 at 𝗠𝗲𝗻𝗮𝗿𝗮 𝗕𝗔𝗖, organised by the 𝗣𝗶𝗻𝗸 𝗥𝗶𝗯𝗯𝗼𝗻 𝗪𝗲𝗹𝗹𝗻𝗲𝘀𝘀 (𝗟) 𝗙𝗼𝘂𝗻𝗱𝗮𝘁𝗶𝗼𝗻 in collaboration with 𝗕𝗲𝗮𝗰𝗼𝗻 𝗛𝗼𝘀𝗽𝗶𝘁𝗮𝗹.

The conference brought together 𝗰𝗹𝗶𝗻𝗶𝗰𝗶𝗮𝗻𝘀, 𝘀𝗰𝗶𝗲𝗻𝘁𝗶𝘀𝘁𝘀, 𝗮𝗻𝗱 𝗯𝗿𝗲𝗮𝘀𝘁 𝗰𝗮𝗻𝗰𝗲𝗿 𝘀𝘂𝗿𝘃𝗶𝘃𝗼𝗿𝘀 for meaningful discussions on 𝗯𝗿𝗲𝗮𝘀𝘁 𝗰𝗮𝗻𝗰𝗲𝗿 𝗰𝗮𝗿𝗲, bridging clinical expertise with patient-centred perspectives. Through 𝗶𝗻𝘀𝗶𝗴𝗵𝘁𝗳𝘂𝗹 𝘁𝗮𝗹𝗸𝘀 𝗮𝗻𝗱 𝗽𝗮𝗻𝗲𝗹 𝗱𝗶𝘀𝗰𝘂𝘀𝘀𝗶𝗼𝗻𝘀, 𝗰𝗼𝗺𝗺𝗼𝗻 𝗺𝗶𝘀𝗰𝗼𝗻𝗰𝗲𝗽𝘁𝗶𝗼𝗻𝘀 𝘄𝗲𝗿𝗲 𝗮𝗱𝗱𝗿𝗲𝘀𝘀𝗲𝗱, and 𝗸𝗲𝘆 𝘂𝗽𝗱𝗮𝘁𝗲𝘀 𝗿𝗲𝗹𝗲𝘃𝗮𝗻𝘁 𝘁𝗼 𝗽𝗿𝗶𝗺𝗮𝗿𝘆 𝗰𝗮𝗿𝗲 𝗽𝗿𝗮𝗰𝘁𝗶𝗰𝗲 𝘄𝗲𝗿𝗲 𝘀𝗵𝗮𝗿𝗲𝗱.

Oncode was honoured to contribute to a day of 𝗹𝗲𝗮𝗿𝗻𝗶𝗻𝗴, 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻, 𝗮𝗻𝗱 𝘀𝗵𝗮𝗿𝗲𝗱 𝗽𝘂𝗿𝗽𝗼𝘀𝗲 in advancing women’s health.

We thank the organisers and participants for making the event truly meaningful.

20/01/2026

𝗘𝗮𝗿𝗹𝘆 𝗱𝗲𝘁𝗲𝗰𝘁𝗶𝗼𝗻 𝘀𝘁𝗮𝗿𝘁𝘀 𝘄𝗶𝘁𝗵 𝗮𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 — 𝗮𝗻𝗱 𝗮𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝘀𝘁𝗮𝗿𝘁𝘀 𝘄𝗶𝘁𝗵 𝗰𝗼𝗻𝘃𝗲𝗿𝘀𝗮𝘁𝗶𝗼𝗻𝘀 𝘁𝗵𝗮𝘁 𝗺𝗮𝘁𝘁𝗲𝗿.

On 𝟳𝘁𝗵 𝗢𝗰𝘁𝗼𝗯𝗲𝗿 𝟮𝟬𝟮𝟱, Oncode was honoured to join 𝘁𝗵𝗲 𝗹𝗮𝘂𝗻𝗰𝗵 𝗼𝗳 𝘁𝗵𝗲 𝗠𝗮𝗺𝗺𝗼𝗴𝗿𝗮𝗺 𝗔𝗱𝘃𝗼𝗰𝗮𝗰𝘆 𝗣𝗿𝗼𝗴𝗿𝗮𝗺 & 𝗣𝗶𝗻𝗸 𝗢𝗰𝘁𝗼𝗯𝗲𝗿 𝗖𝗲𝗹𝗲𝗯𝗿𝗮𝘁𝗶𝗼𝗻 at 𝗨𝗻𝗶𝘃𝗲𝗿𝘀𝗶𝘁𝗶 𝗦𝗮𝗶𝗻𝘀 𝗠𝗮𝗹𝗮𝘆𝘀𝗶𝗮 (𝗨𝗦𝗠) 𝗛𝗲𝗮𝗹𝘁𝗵 𝗖𝗮𝗺𝗽𝘂𝘀, organised by the inspiring team at the 𝗕𝗲𝘀𝘁𝗔𝗥𝗶 𝗨𝗻𝗶𝘁, 𝗨𝗦𝗠 𝗦𝗽𝗲𝗰𝗶𝗮𝗹𝗶𝘀𝘁 𝗛𝗼𝘀𝗽𝗶𝘁𝗮𝗹.

The event brought together 𝗰𝗮𝗻𝗰𝗲𝗿 𝘀𝘂𝗿𝘃𝗶𝘃𝗼𝗿𝘀, 𝗰𝗹𝗶𝗻𝗶𝗰𝗶𝗮𝗻𝘀, 𝗮𝗻𝗱 𝘁𝗵𝗲 𝗽𝘂𝗯𝗹𝗶𝗰 to spotlight the importance of breast health, early detection, and empowering women through knowledge.

🎗 At our booth, we shared the role of 𝗵𝗲𝗿𝗲𝗱𝗶𝘁𝗮𝗿𝘆 𝗰𝗮𝗻𝗰𝗲𝗿 𝗿𝗶𝘀𝗸 𝗮𝘀𝘀𝗲𝘀𝘀𝗺𝗲𝗻𝘁 in helping individuals understand their genetic predisposition — supporting more informed choices in 𝗵𝗲𝗮𝗹𝘁𝗵 𝗺𝗼𝗻𝗶𝘁𝗼𝗿𝗶𝗻𝗴 𝗮𝗻𝗱 𝗽𝗿𝗲𝘃𝗲𝗻𝘁𝗶𝘃𝗲 𝗰𝗮𝗿𝗲.

It was a day of shared strength, meaningful dialogue, and renewed commitment to women's health. Thank you to the 𝗕𝗲𝘀𝘁𝗔𝗥𝗶 𝗨𝗻𝗶𝘁 for the opportunity to contribute to such an impactful initiative.

12/01/2026

On 30th September 2025, Oncode had the privilege of engaging with the Oncology and Radiotherapy Department at Hospital Kuala Lumpur (HKL).

We shared how Oncode’s flexible and customisable panel options deliver high-quality molecular testing at accessible pricing—empowering clinicians with the tools they need for informed decision-making.

A key focus of the session was the critical role of genetic counselling in germline testing. At Oncode, all germline tests are paired with professional genetic counselling, ensuring patients receive not just results, but the support and clarity needed to navigate them confidently.

06/01/2026

From decoding rare mutations to empowering patients with knowledge — 𝗚𝗖𝗔𝗗-𝗡𝗙𝗔𝗗 𝟮𝟬𝟮𝟱 reminded us why genetics is at the heart of precision care.

Oncode was proud to participate in the 𝗚𝗲𝗻𝗲𝘁𝗶𝗰 𝗖𝗼𝘂𝗻𝘀𝗲𝗹𝗹𝗼𝗿 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗗𝗮𝘆 & 𝗡𝗲𝘂𝗿𝗼𝗳𝗶𝗯𝗿𝗼𝗺𝗮𝘁𝗼𝘀𝗶𝘀 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗗𝗮𝘆 𝟮𝟬𝟮𝟱, held at 𝗣𝗲𝗿𝗱𝗮𝗻𝗮 𝗞𝘂𝗮𝗹𝗮 𝗟𝘂𝗺𝗽𝘂𝗿 𝗖𝗶𝘁𝘆 𝗖𝗲𝗻𝘁𝗿𝗲 on 𝟭𝟱–𝟭𝟲 𝗡𝗼𝘃𝗲𝗺𝗯𝗲𝗿, in support of the growing impact of 𝗴𝗲𝗻𝗲𝘁𝗶𝗰 𝗰𝗼𝘂𝗻𝘀𝗲𝗹𝗹𝗶𝗻𝗴 𝗶𝗻 𝗽𝗮𝘁𝗶𝗲𝗻𝘁 𝗰𝗮𝗿𝗲.

The event brought together clinicians, genetic counsellors, patients, and students to explore how 𝗵𝗲𝗿𝗲𝗱𝗶𝘁𝗮𝗿𝘆 𝘁𝗲𝘀𝘁𝗶𝗻𝗴 — from 𝗰𝗮𝗿𝗿𝗶𝗲𝗿 𝘀𝗰𝗿𝗲𝗲𝗻𝗶𝗻𝗴 to 𝗽𝗿𝗲𝗱𝗶𝗰𝘁𝗶𝘃𝗲 𝘁𝗲𝘀𝘁𝗶𝗻𝗴 — is reshaping care pathways and ethical considerations in practice.

🧬 At our booth, we showcased the power of 𝗚𝗲𝗻𝗲𝘁𝗶𝗰 𝗥𝗶𝘀𝗸 𝗔𝘀𝘀𝗲𝘀𝘀𝗺𝗲𝗻𝘁 through our 𝗖𝗔𝗡𝗖𝗘𝗥𝗜𝗦𝗞® 𝗽𝗮𝗻𝗲𝗹 and 𝗿𝗮𝗿𝗲 𝗱𝗶𝘀𝗲𝗮𝘀𝗲 𝘁𝗲𝘀𝘁𝘀, designed to provide 𝗲𝗮𝗿𝗹𝘆, 𝗮𝗰𝘁𝗶𝗼𝗻𝗮𝗯𝗹𝗲 𝗶𝗻𝘀𝗶𝗴𝗵𝘁𝘀.

☕ A highlight was our 𝗺𝗼𝗿𝗻𝗶𝗻𝗴 𝘁𝗲𝗮 𝘁𝗮𝗹𝗸 by Dr Muzhirah Aisha, sharing how 𝗪𝗵𝗼𝗹𝗲 𝗘𝘅𝗼𝗺𝗲 𝗦𝗲𝗾𝘂𝗲𝗻𝗰𝗶𝗻𝗴 (𝗪𝗘𝗦) uncovered a novel mutation, improving diagnostic clarity and guiding more precise, personalised care.

Thank you to everyone who stopped by, listened, and shared. Together, we’re shaping the future of 𝗴𝗲𝗻𝗲𝘁𝗶𝗰 𝗮𝗻𝗱 𝗽𝗿𝗲𝗰𝗶𝘀𝗶𝗼𝗻 𝗵𝗲𝗮𝗹𝘁𝗵𝗰𝗮𝗿𝗲 𝗶𝗻 𝗠𝗮𝗹𝗮𝘆𝘀𝗶𝗮.

31/12/2025

Wishing you a healthy and peaceful year ahead.🫶🏻✨
May 2026 bring strength, healing, and calm to every day.🌿

— Oncode Scientific

24/12/2025

May this joyful season bring hope, health, and peace to us all ✨
Wishing you a Merry Christmas 🎄
— Oncode Scientific

12/12/2025

On 8th November 2025, we were honoured to take part in the 𝗟𝘂𝗻𝗴 𝗖𝗮𝗻𝗰𝗲𝗿 𝗪𝗼𝗿𝗸𝘀𝗵𝗼𝗽: 𝗕𝗮𝗰𝗸 𝘁𝗼 𝗕𝗮𝘀𝗶𝗰𝘀, held in conjunction with 𝗟𝘂𝗻𝗴 𝗖𝗮𝗻𝗰𝗲𝗿 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵.

The workshop emphasised how 𝗺𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗽𝗿𝗼𝗳𝗶𝗹𝗶𝗻𝗴 supports lung cancer care, from the foundations of histopathological evaluation to guiding treatment decisions based on driver mutations detected in advanced disease.

At Oncode Scientific, our mission is clear — to deliver 𝗮𝗰𝗰𝘂𝗿𝗮𝘁𝗲, 𝘁𝗶𝗺𝗲𝗹𝘆, 𝗮𝗻𝗱 𝗮𝗰𝗰𝗲𝘀𝘀𝗶𝗯𝗹𝗲 𝗺𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗱𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰𝘀 that empower physicians and improve outcomes. From 𝘁𝗶𝘀𝘀𝘂𝗲 𝘁𝗼 𝗹𝗶𝗾𝘂𝗶𝗱 𝗯𝗶𝗼𝗽𝘀𝘆, our lung cancer panels are built to support real-world clinical decisions.

Thank you to all the organisers and healthcare professionals who continue to champion education and innovation in cancer care.

25/11/2025

We had an incredible experience at the 𝟯𝟲𝘁𝗵 𝗔𝗻𝗻𝘂𝗮𝗹 𝗦𝗰𝗶𝗲𝗻𝘁𝗶𝗳𝗶𝗰 𝗖𝗼𝗻𝗴𝗿𝗲𝘀𝘀 𝗼𝗳 𝗠𝗮𝗹𝗮𝘆𝘀𝗶𝗮𝗻 𝗢𝗻𝗰𝗼𝗹𝗼𝗴𝗶𝗰𝗮𝗹 𝗦𝗼𝗰𝗶𝗲𝘁𝘆 𝟮𝟬𝟮𝟱 (𝗔𝗦𝗖𝗢𝗠𝗢𝗦 𝟮𝟬𝟮𝟱), engaging with oncologists, internal medicine physicians, surgeons, pathologists, researchers, and other healthcare professionals who share our passion for advancing cancer care. The conference offered a unique opportunity to explore cutting-edge diagnostics, therapeutics, and technologies shaping the future of oncology.

🧬 We were proud to participate in the poster presentation, sharing real-world findings from our 𝗡𝗚𝗦-𝗯𝗮𝘀𝗲𝗱 𝘁𝗲𝘀𝘁𝗶𝗻𝗴 and highlighting how molecular insights guide personalised treatment decisions.

🤝 Our collaborations with pharmaceutical partners reflect a shared commitment to advancing precision oncology — from supporting clinical trials to developing companion diagnostics that enable faster, more informed treatment decisions.

🚀 Driven by continuous R&D, we’re expanding access to 𝗻𝗲𝘅𝘁-𝗴𝗲𝗻𝗲𝗿𝗮𝘁𝗶𝗼𝗻 𝘁𝗲𝘀𝘁𝗶𝗻𝗴 and elevating the standard of 𝗺𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗱𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰𝘀 for patients across Malaysia.

A heartfelt thank you to everyone who visited and engaged with us — your passion inspires our mission to make precision cancer care more accessible and impactful.

Address

Lot 03-01, 3rd Floor. Hap Seng Business Park, No. 12, Persiaran Perusahaan, Unity Square. Seksyen 23, Shah Alam D. E.
Shah Alam
40300

Opening Hours

Monday	09:00 - 18:00
Tuesday	09:00 - 18:00
Wednesday	09:00 - 18:00
Thursday	09:00 - 18:00
Friday	09:00 - 18:00

Telephone

+60333100819

Website

http://www.oncodesc.com/

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About Oncode

ONCODE Scientific Sdn Bhd was founded in 2015, by a strong knowledge-based management and operational team with the combination of more than 85 years of experience in the areas of medical diagnostics and scientific research. It’s aims to be a niche player specializing in Precision Medicine utilizing the techniques of Next Generation Sequencing (NGS), Sanger sequencing, Real-Time & Standard PCR technologies. The team comprises of scientists, geneticists, physicians, pharmacists, bioinformaticians and business veterans who aim to deliver the best quality and affordable molecular diagnostic solutions to the global community.

Oncode laboratory workflows and pipelines include internal and external validation quality controls for compliance with international standards of Good Laboratory Practice (GLP), ISO 15189, the Association for Molecular Pathology (AMP) and the College of American Pathologist (CAP).

The laboratory participates in external quality assurance and proficiency programs including the UK National External Quality Assurance System (UKNEQAS), The European Molecular Genetics Quality Network (EMQN) and the Royal College of Pathologists of Australasia (RCPA).

Oncode Mission

To provide quality diagnostic solutions to customers through the implementation of state-of-the-art laboratory setup designed to worldwide standards, recruitment of dedicated professionals and comprehensive reporting systems.

Oncode Objective

To be a regional one-stop molecular genetics solution center, delivering powerful diagnostic support and insight to medical professionals

关于恩可德

恩可德私人有限公司成立于2015年，由一支强大的知识型管理和运营团队组成，在医疗诊断和科学研究领域拥有超过85年的经验。它的目标是通过提供高科技的下一代基因测序(Next- Generation Sequencing, NGS), Sanger基因测序，实时和标准聚合酶链反(Polymerase-Chain Reaction，PCR) 技术，成为专注于精准医学的利基参与者。该团队由科学家，遗传学家,专科医生，药剂师，生物信息学家和商业资深人士组成，旨在为全球社区提供最优质，价格合理的分子诊断解决方案。

恩可德实验室工作流程和管道包括内部和外验证质量控制，以符合良好实验室规范(Good- Laboratory Practice, GLP)，国际标准化组织（ISO15189），分子病理学协会(Association of Molecular Pathology, AMP)和美国病理学家学会(College of American Pathologist, CAP)的国际标准。

该实验室参与外部质量保证和熟练程序，包括英国国家外部质量保证体系(United Kingdom National External Quality Assurance System, UKNEQAS)，欧洲分子遗传学质量网络(European Molecular Genetics Quality Network)和澳大利亚皇家病理学家学会(Royal College of Pathologists of Australasia, RCPA).

我们的使命

通过实施针对全球标准设计的最先进实验室设置，招聘专业人员和综合报告系统，为客户提供高质量的诊断解决方案。

我们的目标

成为区域性一站式分子遗传学解决方案中心，为医疗专业人员提供强大的诊断支持和洞察力