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TRAINING GRANT IN GENOMIC ANALYSIS AND INTERPRETATION NH GRI Institutional Genomic Science Training GrantsInstructions for 20222023 Application Submission Deadlines for submission of applications:
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How to fill out genomic testing for screening

01
Contact a healthcare provider to order the genomic testing for screening.
02
Provide a sample of your DNA, which can be collected through saliva, blood, or tissue samples.
03
Wait for the results to be processed and analyzed by a genetic counselor or healthcare provider.
04
Discuss the results with your healthcare provider to understand any potential risks or conditions identified through the genomic testing.
05
Follow any recommendations or advice provided by your healthcare provider based on the results of the genomic testing.

Who needs genomic testing for screening?

01
Individuals with a family history of genetic conditions or hereditary diseases.
02
Individuals with a personal history of cancer or other relevant medical conditions.
03
Individuals who are concerned about their risk for inherited conditions or genetic disorders.
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Genomic testing for screening is a process of analyzing a person's DNA to detect any potential genetic mutations or variations that may indicate a higher risk of developing certain diseases.
Individuals who are looking to assess their risk for certain genetic conditions or diseases may choose to undergo genomic testing for screening. However, it is recommended to consult with a healthcare provider or genetic counselor before pursuing this type of testing.
Genomic testing for screening typically involves providing a sample of saliva, blood, or tissue to a laboratory for analysis. The results are then interpreted by a healthcare provider or genetic counselor.
The purpose of genomic testing for screening is to identify potential genetic mutations or variations that may increase an individual's risk of developing certain diseases. This information can help guide personalized healthcare decisions and preventive measures.
The results of genomic testing for screening, including any genetic mutations or variations detected, are typically reported to the individual undergoing the testing and their healthcare provider or genetic counselor.
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