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  1. Home >
  2. Diagnostic Specialties >
  3. Personalized Genomic Medicine >
  4. Genetic Testing >
  5. Sanger Sequencing of Individual Variants

Personalized Genomic Medicine

  • Genetic Testing
    • APOE Genotyping
    • C9orf72 GGGGCC Repeat Expansion
    • Columbia Diagnostic Exome (CDEX)
    • Cystic Fibrosis Screening
    • Fragile X (FMR1) CGG Repeat Expansion
    • mtDNA Whole Genome Sequencing
    • Mitochondrial DNA Depletion
    • Sanger Sequencing of Individual Variants
    • SNP Oligonucleotide Microarray Analysis (SOMA)
    • Southern Blot for Mitochondrial DNA Rearrangements
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Sanger Sequencing of Individual Variants

Purpose

To determine inheritance patterns and possible pathogenicity of variants found by NGS platform-based testing.

CPT Codes

Gene-specific

Methodology

Dideoxyterminator (Sanger) sequencing

Turnaround Time

28 days

Specimen

Blood in EDTA (we can accept a variety of sample types, please contact the lab for more information).

Forms

  • Requisition Form
  • Informed Consent- Identification and Interpretation of a Single Genetic Variant

 

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