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12 Kb Matepair Library Preparation

Original price was: $3,126.Current price is: $2,000.

-36%

The 12 Kb Matepair Library Preparation is an advanced genomic testing method that enables comprehensive analysis of large DNA fragments for structural variant detection. This sophisticated technique creates specialized DNA libraries with 12 kilobase insert sizes, allowing researchers and clinicians to identify complex chromosomal rearrangements, translocations, and genomic structural variations that standard sequencing methods might miss. The test is particularly valuable for cancer genomics research, rare disease diagnosis, and complex genetic disorder investigations. By providing long-range genomic information, it helps uncover hidden genetic abnormalities that contribute to disease development and progression. At just $2000 USD, this cutting-edge testing offers researchers and healthcare providers powerful insights into genomic architecture. The preparation process involves specialized enzymatic treatments and size selection to generate high-quality mate-pair libraries suitable for next-generation sequencing platforms. Results are typically available within 12 days from extracted DNA samples.

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12 Kb Matepair Library Preparation

Comprehensive Introduction to Advanced Genomic Analysis

The 12 Kb Matepair Library Preparation represents a sophisticated genomic testing methodology that revolutionizes how researchers and clinicians analyze complex DNA structures. This advanced technique creates specialized DNA libraries with precisely controlled 12 kilobase insert sizes, enabling comprehensive detection of structural variants and chromosomal abnormalities that traditional sequencing approaches often overlook. As genomic medicine continues to advance, the ability to accurately identify large-scale genomic rearrangements becomes increasingly critical for understanding disease mechanisms and developing targeted treatments.

What This Test Measures and Detects

The 12 Kb Matepair Library Preparation test is designed to identify and characterize:

  • Large structural genomic variants including deletions, duplications, and inversions
  • Complex chromosomal rearrangements and translocations
  • Genomic insertions and copy number variations exceeding standard detection limits
  • Chromosome breakpoints and fusion events
  • Large-scale genomic architecture abnormalities
  • Complex rearrangement patterns in cancer genomes

Who Should Consider This Advanced Testing

This specialized genomic preparation is particularly valuable for:

  • Research institutions investigating complex genetic disorders
  • Oncology centers studying cancer genome evolution and heterogeneity
  • Clinical geneticists diagnosing rare diseases with suspected structural variants
  • Academic researchers exploring genomic architecture and evolution
  • Pharmaceutical companies developing targeted therapies
  • Diagnostic laboratories requiring comprehensive structural variant analysis

Significant Benefits of 12 Kb Matepair Testing

Choosing our 12 Kb Matepair Library Preparation offers numerous advantages:

  • Comprehensive Structural Analysis: Detect large genomic variants that short-read sequencing misses
  • Enhanced Resolution: 12 kilobase insert size provides optimal balance between coverage and resolution
  • Research Quality Data: Generate publication-ready genomic data for scientific studies
  • Clinical Insights: Uncover hidden genetic abnormalities contributing to disease
  • Cost-Effective Solution: Advanced testing at competitive pricing
  • Rapid Turnaround: Results typically available within 12 days

Understanding Your Test Results

Your 12 Kb Matepair Library Preparation results will provide detailed information about:

  • Quality metrics of the prepared library including concentration and size distribution
  • Assessment of library complexity and potential sequencing performance
  • Verification of proper 12 kb insert size achievement
  • Recommendations for downstream sequencing applications
  • Technical parameters for optimal sequencing run configuration

Our expert genetic counselors and bioinformaticians are available to help interpret complex results and guide next steps in your research or diagnostic journey.

Test Pricing Information

Service Description Price (USD)
12 Kb Matepair Library Preparation – Discount Price $2000
12 Kb Matepair Library Preparation – Regular Price $3126

Nationwide Testing Availability

GGC DNA provides comprehensive 12 Kb Matepair Library Preparation services across the United States. We have established testing facilities in major metropolitan areas including:

  • New York City and surrounding regions
  • Los Angeles and Southern California
  • Chicago and Midwest locations
  • Houston and Texas medical centers
  • Philadelphia and Northeast corridors
  • Phoenix and Southwest regions
  • San Antonio and additional Texas locations
  • San Diego and coastal California
  • Dallas and North Texas areas
  • San Jose and Silicon Valley

Schedule Your Advanced Genomic Testing Today

Take the next step in your genomic research or clinical diagnostics with our state-of-the-art 12 Kb Matepair Library Preparation. Our specialized team is ready to assist you with sample submission, technical consultations, and result interpretation.

Call us now at +1(267) 388-9828 to schedule your test or speak with our genomic specialists. We’re available to answer your questions about sample requirements, turnaround times, and how this advanced testing can benefit your specific research or clinical needs.

For researchers and clinicians requiring the highest quality genomic data, our 12 Kb Matepair Library Preparation offers unparalleled insights into complex genetic architectures. Contact us today to discover how this cutting-edge technology can advance your scientific investigations or improve patient diagnostics.