Human Genome Sequencing and Variant Calling 30X Test - $5
Sale!

Human Genome Sequencing and Variant Calling 30X

Original price was: $7,500.Current price is: $5,626.

-25%

Human Genome Sequencing and Variant Calling 30X represents the pinnacle of genetic testing technology, providing comprehensive analysis of your entire DNA blueprint. This advanced test sequences your complete genome at 30X coverage depth, ensuring exceptional accuracy in identifying genetic variants, mutations, and potential health markers. The test examines all 20,000-25,000 genes in the human genome, offering unprecedented insights into inherited conditions, disease predispositions, and personalized health optimization. Results are delivered within 8 weeks and require only extracted DNA sample. At just $5,626 USD (discounted from $7,500), this comprehensive genetic assessment provides lifelong value for proactive health management and informed medical decision-making.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

Human Genome Sequencing and Variant Calling 30X

Comprehensive Genetic Blueprint Analysis

Human Genome Sequencing and Variant Calling 30X represents the most advanced level of genetic testing available today. This cutting-edge technology provides a complete readout of your entire DNA sequence, offering unprecedented insights into your genetic makeup and potential health predispositions. Unlike targeted genetic tests that examine specific genes or regions, whole genome sequencing analyzes all 3 billion base pairs of your DNA, creating a comprehensive genetic profile that can inform healthcare decisions throughout your lifetime.

What This Test Measures and Detects

Our 30X coverage whole genome sequencing provides exceptional accuracy in identifying:

  • Complete DNA sequence analysis across all chromosomes
  • Single nucleotide variants (SNVs) and polymorphisms
  • Insertions and deletions (indels) of genetic material
  • Copy number variations (CNVs) and structural variants
  • Mitochondrial DNA mutations
  • Rare genetic variants with clinical significance
  • Pharmacogenetic markers affecting drug metabolism
  • Ancestry and population-specific genetic markers

Who Should Consider This Test

This comprehensive genetic analysis is particularly valuable for:

  • Individuals with unexplained medical conditions or complex symptoms
  • Those with family histories of genetic disorders or hereditary cancers
  • Couples planning pregnancy who want comprehensive carrier screening
  • Patients seeking personalized medicine approaches to treatment
  • Individuals interested in proactive health optimization and disease prevention
  • People with rare or undiagnosed conditions seeking genetic answers
  • Those wanting comprehensive pharmacogenetic information for medication management

Benefits of Comprehensive Genome Sequencing

Choosing whole genome sequencing provides numerous advantages:

  • Lifelong Genetic Reference: Your genome sequence remains constant, providing a permanent resource for future healthcare needs
  • Comprehensive Coverage: Unlike panel tests, whole genome sequencing captures all genetic information in a single analysis
  • Future-Proof Results: As genetic research advances, your existing genome data can be re-analyzed for new discoveries
  • Personalized Health Insights: Understand your unique genetic predispositions for targeted prevention strategies
  • Family Health Planning: Identify inherited conditions that could affect future generations
  • Medication Optimization: Receive guidance on which medications may work best based on your genetic profile

Understanding Your Test Results

Your comprehensive genome report will include:

  • Primary Findings: Clinically significant variants with established medical implications
  • Secondary Findings: Additional genetic variants that may impact health management
  • Carrier Status: Information about genetic conditions you could pass to children
  • Pharmacogenetic Insights: How your body processes various medications
  • Ancestry Information: Genetic heritage and population origins
  • Lifestyle Factors: Genetic influences on nutrition, exercise response, and more

All results are reviewed by our team of certified genetic counselors who provide personalized explanations and recommendations based on your specific genetic profile.

Test Pricing and Details

Test Component Details
Test Name Human Genome Sequencing and Variant Calling 30X
Discount Price $5,626 USD
Regular Price $7,500 USD
Turnaround Time 8 weeks
Sample Type Extracted DNA

Nationwide Availability

GGC DNA has testing facilities conveniently located across the United States, serving major metropolitan areas including New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee. Our network of certified genetic counselors and medical professionals ensures you receive comprehensive support throughout your genetic testing journey.

Take Control of Your Genetic Health Today

Your genetic blueprint holds the key to understanding your health potential and risks. With Human Genome Sequencing and Variant Calling 30X, you gain access to the most complete genetic information available, empowering you to make informed decisions about your health and wellness. Our team of genetic specialists is ready to guide you through the process and help you understand what your DNA reveals about your unique health profile.

Ready to unlock the secrets of your DNA? Book your Human Genome Sequencing and Variant Calling 30X test today by calling our genetic specialists at +1(267) 388-9828 or schedule your appointment online. Take the first step toward personalized, genetically-informed healthcare.

SKU: fbd85d9451c0 Category: