Next-Generation Sequencing (NGS)

Next-Generation Sequencing (NGS) for Precision Cancer Detection & Immunotherapy Planning

In today’s oncology, precision begins at the molecular level. Next-Generation Sequencing (NGS) doesn’t just decode your DNA; it unlocks a complete biological map that helps oncologists target cancer more accurately than ever before. At Neeli Genetics, NGS is integrated into a multi-omic platform that guides powerful immunotherapies like Clavi-Q-RE, bringing personalised, non-toxic, and highly targeted care within reach.

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NGS for Cancer
Sample Type
Blood, tissue, or tumour biopsy
Sample Size
Varies by test
Cancers Supported
Breast, lung, colorectal, ovarian, and more
Turnaround Time
10-14 days

What Makes NGS So Effective in 2025?

NGS provides deep insights across 4 biological layers of your tumour’s profile:

Genetic Sequencing – Detects cancer-driving DNA mutations (e.g., BRCA1/2, KRAS, EGFR)
Epigenetic Mapping – Reveals methylation silencing of tumour suppressor or immune escape genes
Transcriptomics – Highlights which genes are actively pushing tumour growth
Proteomics – Uncovers immune checkpoints and surface antigens that guide therapy

Together, these data layers fuel the RGCC Onconomics Plus, Oncotrace, and Immune Frame panels, turning test results into personalised action plans.

How It Helps

Cancer Treatment Just Got Personal and Powerful

In 2025, cancer treatment starts not with a guess but with your genetic code. At Neeli Genetics, Next-Generation Sequencing is more than a test; it’s the foundation of personalised, immune-guided, and evidence-based care. You’re not just detecting cancer, and you’re outsmarting it.

Faster Identification of Actionable Targets ,Quickly pinpoint which mutations or immune markers matter most for treatment.
Minimised Toxicity By matching treatment to biology, unnecessary exposure to chemotherapy is reduced.
Higher Response Rates Multi-omic diagnostics help identify resistance pathways early, improving therapeutic precision.
Eligibility for Advanced Therapies NGS is a gateway to immunotherapies like Clavi-Q-RE, CAR-T, PARP inhibitors, and more.

Why choose Next-Generation Sequencing (NGS)?

India’s leading RGCC diagnostic partner.
Full oncogenetic counselling and care coordination

Integrated genetic, epigenetic, transcriptomic, and proteomic analysis

Certified for Clavi-Q-RE, Q-REstrain, Immune Frame, and Onconomics protocols

How to Access NGS with Neeli Genetics

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Sample Collection

Blood draw or biopsy can be arranged at any Neeli Genetics-affiliated clinic or hospital.

30-minute-appointments

Multi-Omic Profiling

Your DNA, RNA, and protein profiles are analysed using RGCC-accredited panels.

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Report & Interpretation

You’ll receive a precision oncology report with therapy guidance aligned to global best practices.

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Next Steps with Our Clinical Experts

Our team helps you and your oncologist translate your results into a personalised treatment plan, often including immunotherapy.

Ready to Activate Your Body’s Defenses? Book Your Consultation Now

    Frequently Asked Questions

    • What is Next-Generation Sequencing (NGS) and how is it used in cancer care?

      NGS is a powerful diagnostic tool that analyses genetic, epigenetic, transcriptomic, and proteomic information from a blood, tissue, or tumour sample. It helps identify specific mutations and biomarkers that drive cancer, enabling oncologists to create highly personalised and targeted treatment plans.

    • Which cancers can be analysed with NGS?

      NGS is suitable for a wide range of cancers, including breast, lung, colorectal, ovarian, and many others. It is especially helpful when selecting targeted therapies or determining eligibility for advanced treatments like Clavi-Q-RE immunotherapy or PARP inhibitors.

    • How is the sample collected for NGS?

      Samples can be collected through a blood draw, tissue sample, or tumour biopsy. The exact type and size of the sample may vary depending on the test being conducted and the location of the cancer.

    • How soon can I get the results?

      Turnaround time is typically 10–14 days, after which you’ll receive a detailed precision oncology report outlining actionable mutations, therapeutic targets, and potential immunotherapy options.

    • Why choose Neeli Genetics for NGS testing?

      Neeli Genetics is a leading RGCC diagnostic partner in Hyderabad, India, offering multi-omic profiling across genetic, epigenetic, transcriptomic, and proteomic levels. The results are directly integrated into personalised cancer care plans and immunotherapies like Clavi-Q-RE, ensuring global-standard precision with local access.