Whole Mitochondrial Genome Sequencing With MCC
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The Whole Mitochondrial Genome Sequencing with MCC test is an advanced genetic diagnostic assay that sequences the entire mitochondrial DNA (mtDNA) to identify mutations, variants, and heteroplasmy. This test is combined with Maternal Cell Contamination (MCC) analysis to ensure the accuracy and reliability of results, especially in prenatal or reproductive genetic testing.
Test Method: Next-Generation Sequencing (NGS) with MCC Analysis
Sample Type: Blood or Buccal Swab
Turnaround Time: Typically 14–21 days
Key Benefits:
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✅ Comprehensive analysis of the entire mitochondrial genome
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✅ Detects pathogenic mutations associated with mitochondrial disorders
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✅ MCC check ensures sample integrity and result accuracy
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✅ Supports prenatal, reproductive, and clinical genetic counseling
Formula Highlights:
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High-coverage NGS for precise detection of heteroplasmy
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Bioinformatic pipeline identifies clinically significant variants
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MCC analysis minimizes risk of false-positive or false-negative results
Usage Instructions:
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Collect blood or buccal swab following proper collection protocols
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Ensure correct labeling and documentation for sample submission
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Follow physician or genetic counselor guidance for result interpretation
Additional Information:
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Recommended for patients with suspected mitochondrial disorders, unexplained metabolic conditions, or family history of mitochondrial disease
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Interpretation should be done by a certified geneticist or counselor
What You Receive:
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Detailed laboratory report of mtDNA variants and pathogenic mutations
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MCC verification summary to confirm sample integrity
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Genetic counseling notes to guide clinical management
Safety & Care:
Free From:
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