Whole Exome Sequencing (WES) + MCC

2 Tests | Rs 21500 | Blood Tests Only | Fasting Not Needed
Powered By Redcliffelab
Maternal Cell Contamination (MCC) (1) Whole Exome Sequencing (WES) (1)
  1. Maternal Cell Contamination (MCC) (1)
    1. Maternal Cell Contamination (MCC)
  2. Whole Exome Sequencing (WES) (1)
    1. Whole Exome Sequencing (WES)

 
Maternal Cell Contamination (MCC) and Whole Exome Sequencing (WES). Here’s a breakdown of the tests and some additional information:

  1. Maternal Cell Contamination (MCC): This test is designed to detect maternal cell contamination in a fetal sample. During pregnancy, a small number of fetal cells can circulate in the maternal bloodstream. Detecting and isolating these cells is important for certain genetic tests, especially when analyzing fetal DNA. MCC testing ensures that the genetic analysis is accurate and reflects the true genetic information of the fetus.
  2. Whole Exome Sequencing (WES): Whole Exome Sequencing is a technique that examines the exome, which is the portion of the genome that contains all the protein-coding genes. It allows scientists and clinicians to identify genetic variations, mutations, and potential disease-causing variants in these specific regions. WES can be helpful in diagnosing certain genetic disorders or understanding the genetic basis of various diseases.

Details of the package:

  • The package includes both the Maternal Cell Contamination (MCC) test and the Whole Exome Sequencing (WES) test.
  • The cost of the package is Rs 21,500.
  • The tests require a blood sample, and fasting is not needed before the test.

The testing service is powered by Redcliffelab, which is likely the laboratory or company conducting the genetic testing and analysis.

If you are considering undergoing these tests, it’s essential to consult with a healthcare professional or a genetic counselor to understand the implications and benefits of the tests and to interpret the results accurately. Genetic testing can provide valuable insights into health risks and potential genetic conditions but should be approached with informed consent and proper medical guidance.

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