Precision oncology for the Philippines

Advancing Precision Cancer Care in the Philippines

Through advanced genomic testing, clinical expertise and global collaborations, LINCS helps bring personalised cancer care closer to Filipino patients.

About Us

Empowering Genomics, Enriching Lives

At Linking Network for Cancer Services Inc. (L!NCS), we believe that precision genomics should be accessible to every Filipino patient, healthcare professional, researcher, and healthcare institution.

Founded with a mission to transform healthcare and research through next-generation sequencing (NGS), our lab is equipped with the latest technology, guided by experts in molecular biology, bioinformatics, and clinical diagnostics.

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Our Leadership

The Experts Steering Our NGS Vision

A dynamic team of reputable key opinion leaders known in cancer care, driving precision oncology across the Philippines.

Catherine SC Teh, M.D.

Catherine SC Teh, M.D.

Chair of the Board

Necy S. Juat, M.D.

Necy S. Juat, M.D.

President & CEO

Jhade Lotus P. Peneyra

Jhade Lotus P. Peneyra

Finance & Gen. Support Director

Annielyn Ong-Cornel, M.D.

Annielyn Ong-Cornel, M.D.

Sales & Marketing Director

Christina G. Galvez, M.D.

Christina G. Galvez, M.D.

Laboratory & Research Director

Our Network & Labs

Delivering innovation and impact through our global presence and advanced genomics labs.

Manila, Philippines

Hub · SE Asia Genomics Lab

Our Southeast Asia Genomics Lab in Manila drives cutting-edge research and innovation in genomics, bioinformatics, and precision medicine to improve lives across the region.

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Our lab

State-of-the-art facilities enabling world-class genomics research.

Laboratory scientist loading a cartridge into a sequencer
Laboratory scientist preparing samples with a pipette
Laboratory scientist loading samples into a benchtop analyser
Laboratory scientist handling a sample rack at a lab bench
Laboratory scientist operating a centrifuge
Scientist starting a sequencing run on a sequencer
Close-up of an Illumina sequencer with a loaded cartridge
Illumina sequencer close-up inside the genomics lab
Sequencer bench inside the glass-walled laboratory
Laboratory scientist in the Manila genomics lab
Our Test Panels

Genomic Testing Solutions

From focused panels to whole-exome profiling, TARGT delivers actionable genomic insights for solid tumors, hereditary cancers, and complex cases.

TARGT First

Your First Step in Precision Oncology

TARGT First is one of the most focused and affordable pan-solid Cancer Gene panels available, featuring 92 of the most commonly mutated cancer-associated genes with a high level of evidence for both targeted therapy and prognostication.

"Your First Step in Precision Oncology."

92
Actionable Cancer Genes
15 working days
TAT
Why it works

Cost-effective, focused panel covering the most frequently mutated genes in solid tumors.

TARGT Indiegene

Genomics Grounded in Your Community

TARGT Indiegene is a cancer gene panel developed by comprehensively profiling the whole-exome and transcriptome of 3,000+ tumor samples from cancer patients, covering 28 cancer types.

"Genomics Grounded in Your Community."

1,212
Unique Genes
15 working days
TAT
Why it works

Developed on data from 1,500+ Asian patients across 28 cancer types to boost effectiveness in Asia-Pacific populations.

TARGT Absolute

Beyond the Standard Cancer CGP Panel

TARGT Absolute provides a comprehensive report based on whole-exome profiling to match targeted therapy with biomarkers. It uses Cellworks' advanced AI-based Biosimulation Platform.

"From Tissue and Blood, Into Action."

20,000+
Genes Profiled
21 working days
TAT
Why it works

Absolute SoLiQ analyzes ~20,000 genes using dual solid/liquid biopsies - ideal for challenging or rare cases.

Hereditary Cancer Panels

Know Their Genes, Shape Their Futures

From Risk to Response. Guided by Genes. Detects inherited mutations from both parents for all cancer types to enable early prevention and personalized care planning.

"Know Their Genes, Shape Their Futures."

15
to 163 Genes
15 working days
TAT
Why it works

This panel detects inherited mutations to enable early prevention and personalized care planning.

Not sure which panel is right for you?
Talk to our care team →
Built for everyone in the network

One platform. Four audiences.

Whether you are a patient, a clinician, a researcher, or a sponsor — there is a path into precision oncology through LINCS.

For Patients

Book a genomic appointment and track its progress, view test results, and reach our team — all in one place.

For Hospitals & Clinics

Onboard your site to our partner network, integrate lab workflows, and bring advanced genomic testing to your patients.

For Researchers

Collaborate on clinicogenomic datasets representing the genomic diversity of the Philippines and Southeast Asia.

For Industry

Accelerate clinical trial recruitment and biomarker discovery with real-world, multi-modal genomic evidence.

Get Involved

Ready to Join the Fight?

Whether you are a patient, provider, or organization, there is a place for you in the LINCS network. Together, we improve quality of care and patient safety.

200+
Partners
10k+
Patients
50+
Programs
FAQ

Frequently Asked Questions

Everything you need to know about booking, testing, and partnering with LINCS.

Still have questions? Reach out to our team — we typically respond within one business day.