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Reports Within

Parameters

Reports Within:

Parameter Include:

Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

  1. Standard TAT: 60 days
  2. Routine TAT: 90 days
  3. Extended TAT: 180 days

What are the prerequisites for the test Clinical Exome Seqencing Test

  • Physician order for Clinical Exome Sequencing Test
  • Completed patient consent form
  • Medical history and family history information
  • Insurance pre-authorization, if required

What are the measure values for the test Clinical Exome Seqencing Test

  • Sequencing Depth: 100X
  • Coverage: >98% at 20X
  • Accuracy: >99.9%
  • Variants Detected: SNVs, indels, CNVs
  • Turnaround Time: 4-6 weeks

What does this test Clinical Exome Seqencing Test identify?

The Clinical Exome Sequencing Test identifies genetic variations in the exome, which is the portion of the genome that contains protein-coding genes. This test can help diagnose rare genetic disorders, identify disease-causing mutations, and guide personalized treatment options for patients. By analyzing thousands of genes simultaneously, this test can provide valuable insights into a patient's genetic makeup and potential risk factors for certain diseases.

Why is this test Clinical Exome Seqencing Test taken?

The Clinical Exome Sequencing Test is taken to identify genetic mutations that may be responsible for a patient's symptoms or condition. This test analyzes the protein-coding regions of the genome, known as the exome, which are responsible for producing proteins that carry out essential functions in the body.

By sequencing the exome, healthcare providers can identify mutations that may be causing a patient's symptoms or condition, leading to a more accurate diagnosis and potentially guiding treatment decisions. This test is particularly useful for patients with rare or undiagnosed genetic conditions, as it can uncover genetic variants that may not be detected by other tests.

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