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Panel Testing

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Panel Testing

Panel testing also known as Multi Gene Testing, is a genetic testing method that analyzes multiple genes in a single test to identify mutations linked to specific diseases or conditions. Unlike single gene tests, panel testing provides a broader, more comprehensive view of a person’s genetic makeup. It’s commonly used for hereditary cancer, heart disease, neurological disorders, and carrier screening. By using technologies like Next-Generation Sequencing , it delivers faster, cost-effective, and accurate results. Panel testing helps doctors make informed medical decisions, supports early diagnosis, and assesses inherited risks for families. It’s ideal for individuals with complex symptoms or a family history of genetic conditions.

Why Choose This Panel Testing?

Panel testing is a smart, efficient choice for individuals seeking a deeper understanding of their genetic health. By analyzing multiple genes in a single test, it offers comprehensive coverage that increases the chances of identifying the underlying cause of a condition. This approach is faster and more cost-effective than testing one gene at a time. It focuses on genes with known clinical relevance, allowing healthcare providers to deliver more accurate diagnoses and personalized treatment plans. Panel testing also uncovers inherited risks, providing valuable information for both the individual and their family, and empowering proactive, preventive healthcare decisions.

When Is It Used?
  • Family history of genetic disorders
  • Multiple related symptoms with unclear cause
  • Suspected hereditary cancer or heart disease
  • Unexplained developmental delays or neurological issues
  • Carrier screening before or during pregnancy
  • To guide personalized treatment or medication response
Who Should Consider Panel Testing?

Panel testing is ideal for individuals who may have a higher risk of genetic conditions due to personal or family medical history. It provides valuable insights that can lead to early detection, targeted treatment, and informed health decisions. You should consider panel testing if:

You should consider this test if:

  • You have a family history of inherited diseases like cancer, heart disorders, or neurological conditions.
  • You are experiencing symptoms that may be linked to multiple genes.
  • You’ve had negative or inconclusive results from single-gene tests.
  • You are planning a family and want to assess carrier status for inherited conditions.
  • You need personalized treatment guidance, such as medication response or disease risk.
  • You want to understand and manage your genetic health proactively.
How We Work
How is the Test Performed?

Step 1

Sample Collection

A blood or saliva sample is collected from the patient.

Step 2

DNA Extraction

The lab extracts DNA from the collected sample.

Step 3

Gene Sequencing

Using Next-Generation Sequencing (NGS), multiple genes are analyzed simultaneously.

Step 4

Data Analysis

Genetic specialists examine the sequencing data for mutations or variants.

Step 5

Result Compilation

Findings are compiled into a detailed, easy-to-understand report.

Step 6

Consultation

Results are reviewed with a healthcare provider or genetic counselor for interpretation and next steps.

Our Services
Just a few of the many health issues we screen for
Colorectal Cancer Risk

Screens for gene variants linked to colorectal, endometrial, and other cancers caused by mismatch repair gene mutations in families.

Long QT Syndrome

Assesses genes responsible for abnormal heart rhythms that can lead to fainting, seizures, or sudden death, often triggered by stress.

Spinal Muscular Atrophy

Identifies mutations in the SMN1 gene that lead to progressive muscle weakness and movement difficulties, often beginning in infancy.

Fragile X Syndrome

Detects mutations in the FMR1 gene that cause intellectual disability, developmental delays, and behavioral challenges, especially in boys and men.

Marfan Syndrome

Screens for FBN1 gene mutations linked to connective tissue disorder affecting heart, eyes, and skeleton, with risk of life-threatening aortic rupture.

Phenylketonuria

Detects PAH gene mutations leading to inability to break down phenylalanine, causing intellectual disability if untreated from early infancy.

Who we Are
Why Choose Us?
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State-of-the-Art Digital Lab Experience

Our fully integrated E-Lab platform offers online test ordering, real-time tracking, and secure digital reporting bringing convenience and control to both physicians and patients across the country.

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Advanced Diagnostic Technology

From routine blood tests to complex genetic panels, we leverage cutting-edge platforms like NGS, PCR, and AI-powered analytics for maximum accuracy and clinical relevance.

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Fast Turnaround, Local Support

With lab facilities based in Florida, we ensure faster processing times and direct access to our expert team. You get timely results backed by responsive, local customer support.

Get your free estimate!

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