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2×150 HiSeq Sequencing 5 GB

Original price was: $500.Current price is: $312.

-38%

The 2×150 HiSeq Sequencing 5 GB test represents cutting-edge next-generation sequencing technology that provides comprehensive genomic analysis. This advanced diagnostic tool sequences DNA with 150 base pair reads in both directions, delivering 5 gigabytes of high-quality genetic data. The test is essential for researchers, clinicians, and individuals seeking detailed genetic information for various applications including disease research, ancestry analysis, and personalized medicine. With a 4-week turnaround time and requiring only extracted DNA samples, this test offers unparalleled insights into genetic makeup. The discounted price of $312 USD makes this sophisticated technology accessible for comprehensive genetic assessment and research purposes across the United States.

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2×150 HiSeq Sequencing 5 GB: Advanced DNA Sequencing Technology

Comprehensive Introduction to Next-Generation Sequencing

The 2×150 HiSeq Sequencing 5 GB test represents the pinnacle of modern genetic analysis technology, utilizing Illumina’s HiSeq platform to deliver unprecedented genomic insights. This sophisticated sequencing method employs paired-end 150 base pair reads, providing bidirectional coverage that significantly enhances data accuracy and reliability. The 5 GB data output capacity ensures comprehensive genomic coverage, making this test an invaluable tool for both clinical diagnostics and research applications.

Next-generation sequencing has revolutionized genetic medicine by enabling rapid, cost-effective analysis of entire genomes or targeted regions. The 2×150 configuration specifically refers to the sequencing of 150 base pairs from both ends of DNA fragments, creating overlapping reads that improve assembly accuracy and detect structural variations that single-read methods might miss.

What This Advanced Sequencing Test Measures

The 2×150 HiSeq Sequencing 5 GB test provides comprehensive genetic analysis through:

  • High-Resolution DNA Sequencing: Captures 150 base pair reads from both ends of DNA fragments
  • Comprehensive Genomic Coverage: Generates 5 gigabytes of sequencing data for detailed analysis
  • Variant Detection: Identifies single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variations
  • Quality Metrics: Provides detailed quality scores and coverage statistics for reliable interpretation
  • Paired-End Advantages: Enables better mapping, improved variant calling, and detection of complex rearrangements

Who Should Consider This Advanced Genetic Test

This comprehensive sequencing test is ideal for:

  • Research Institutions: Academic and pharmaceutical researchers requiring high-quality genomic data
  • Clinical Laboratories: Healthcare providers seeking detailed genetic information for complex cases
  • Genetic Counselors: Professionals needing comprehensive data for inheritance pattern analysis
  • Individuals with Complex Medical Histories: Patients with undiagnosed genetic conditions
  • Ancestry and Genealogy Researchers: Those seeking detailed genetic lineage information
  • Personalized Medicine Applications: Individuals interested in comprehensive genetic profiling

Significant Benefits of 2×150 HiSeq Sequencing

Choosing this advanced sequencing technology provides numerous advantages:

  • Unparalleled Accuracy: Paired-end sequencing reduces errors and improves data reliability
  • Comprehensive Data: 5 GB output ensures thorough genomic coverage
  • Research-Grade Quality: Meets standards for publication and clinical validation
  • Time Efficiency: 4-week turnaround time for comprehensive results
  • Cost-Effective Solution: Advanced technology at an accessible price point
  • Future-Proof Data: Raw sequencing data can be reanalyzed as new discoveries emerge

Understanding Your Sequencing Results

Your 2×150 HiSeq Sequencing results will include comprehensive data presented in multiple formats:

  • Raw Sequencing Files: FASTQ format containing all sequencing reads with quality scores
  • Alignment Data: BAM files showing how sequences map to reference genomes
  • Variant Calling: VCF files detailing genetic variations identified
  • Quality Metrics: Detailed reports on sequencing depth, coverage, and data quality
  • Interpretation Guidance: Basic analysis of significant findings with recommendations for further investigation

It’s important to consult with genetic specialists to fully interpret these complex results. The comprehensive nature of this data requires professional analysis to extract clinically relevant information and understand implications for health, ancestry, or research objectives.

Test Pricing and Availability

Price Type Amount (USD)
Discount Price $312
Regular Price $500

Nationwide Accessibility

We proudly serve patients and researchers across the United States with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified laboratories ensures consistent quality and reliable service nationwide.

Schedule Your Advanced Genetic Sequencing Today

Take the next step in genetic discovery with our state-of-the-art 2×150 HiSeq Sequencing service. Our team of genetic specialists is ready to assist you with sample collection, testing coordination, and result interpretation.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your test or discuss your specific sequencing needs. Our genetic counselors are available to answer your questions and help you understand how this advanced technology can benefit your research or healthcare journey.

With a 4-week turnaround time and requiring only extracted DNA samples, this comprehensive sequencing service provides the detailed genetic information you need for informed decision-making and groundbreaking research. Don’t miss this opportunity to access cutting-edge genomic technology at our special discounted rate of $312 USD.