NGS Testing Services Built for Precision and Trust
We bring together diagnostic products, laboratory testing, and public health screening to make advanced genomic testing more accessible.
Understanding NGS
How Does NGS Testing Work?
Next-Generation Sequencing is a technology that reads DNA in a way that's faster and more detailed than older methods. Instead of analysing one piece of genetic code at a time, it processes millions of DNA fragments together, giving a fuller picture in far less time.
This makes it possible to study genes more closely, whether the goal is understanding a disease, guiding treatment decisions, or supporting research. For patients and clinicians alike, it means access to answers that support faster, more informed decisions.
USES
How NGS Applies
NGS APPLICATIONS
Prenatal Genetics
Through non-invasive prenatal testing, NGS offers expecting parents safe, early insight into their baby's genetic health
NGS APPLICATIONS
Infectious Diseases
NGS helps identify infectious agents with precision, supporting faster diagnosis and more informed treatment planning for patients.
NGS APPLICATIONS
Genetic Insight
NGS enables detailed genetic analysis, helping identify inherited conditions and supporting more personalised approaches to patient care.
NGS APPLICATIONS
Maternal Health
NGS supports newborn screening, helping identify health risks early for both mother and baby.
NGS APPLICATIONS
Cancer Genomics
NGS helps identify genetic mutations linked to cancer, supporting more targeted, informed treatment decisions for patients.
NGS APPLICATIONS
General Wellness
NGS supports general health screening, helping individuals and providers stay ahead of potential health risks early
NGS Test Categories Overview
NGS helps identify infectious agents with precision, supporting faster diagnosis and more informed treatment planning for patients.
Non-Invasive Prenatal Testing (NIPT)
Screens fetal chromosomal abnormalities safely using cell-free DNA from maternal blood.
Preimplantation Genetic Testing (PGT)
Screens embryos for chromosomal abnormalities before transfer, improving IVF success rates.
Oncomine Comprehensive Assay
Profiles up to 500+ cancer-related genes, with a focused 161-gene panel available.
Oncomine Focus Assay
Identifies actionable genomic alterations in solid tumors using a targeted panel.
Pan Cancer Liquid Biopsy
Analyzes circulating tumor DNA from plasma for minimally invasive cancer monitoring.
Hereditary Cancer Panel
Identifies inherited mutations linked to breast, ovarian, colorectal cancers, and Lynch syndrome.
HLA Typing (High Resolution)
Identifies HLA alleles accurately, supporting reliable donor matching and reduced rejection risk.
Bacteria Identification Panel (Gut Microbiome)
Profiles gut bacterial communities using 16S rRNA sequencing for research insights.
OUR STRENGTHS
Supporting high-volume screening initiatives with molecular diagnostic solutions and workflows built for wider programme implementation.
OUR STRENGTHS
Making advanced diagnostic technologies more accessible through cost-conscious solutions suited to underserved and low-resource settings.
OUR STRENGTHS
Providing technical guidance, training, troubleshooting, and operational support to help partners run diagnostic workflows effectively.
OUR STRENGTHS
Supporting the screening journey with diagnostic testing, data capture, and reporting capabilities that help partners manage programmes efficiently.
Got Questions?
We've Got Answers
Everything you need to know about this test, from booking to results.
Contact
admin@medinno.inWhat is NGS testing?
Next-Generation Sequencing is an advanced technology that reads DNA in detail, helping identify genetic changes linked to health conditions. It's used across areas like oncology, prenatal screening, and infectious disease detection, offering deeper insight than many traditional testing methods.
Who should consider NGS testing?
NGS testing may be recommended by a doctor for patients with a family history of genetic conditions, those undergoing cancer treatment, expecting parents seeking prenatal screening, or anyone needing detailed genetic insight to guide diagnosis or treatment decisions.
What sample is required for testing?
Most NGS tests require a simple blood sample, though some tests may need a tissue sample depending on the specific condition being screened. Your healthcare provider will confirm the exact requirement based on the test you're undergoing.
How long does it take to get results?
Processing time depends on the specific test and panel you choose. Once we receive and process your sample, our laboratory team works to deliver accurate results within a reasonable timeframe.
Is NGS testing safe?
Yes. Most NGS testing involves a standard blood draw, similar to routine lab work. For prenatal testing specifically, it's non-invasive and carries no risk to the pregnancy, unlike more invasive diagnostic procedures.
How do I understand my test report?
Your report will include a clear summary of findings, explained in plain language alongside technical detail. If you have questions, our specialist team is available to walk you through the results with you.
Do I need a doctor's referral to get tested?
This depends on the specific test. Some screenings can be booked directly, while others may require a referral from your physician. Our team can help clarify what's needed for the test you're interested in.