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MEDICAL GENOMICS LABORATORY UAB MEL Accession720 Twentieth Street South, Suite 330 Phone: (205) 9345562 Birmingham, Alabama 352940005 Fax: (205) 9962929 www.uab.edu/medicine/genetics/medicalgenomicslaboratory

How to fill out next-gen sequencing and deletionduplication

How to fill out next-gen sequencing and deletionduplication

1. Gather the necessary samples and information regarding the individual or individuals being tested.
2. Choose a reputable laboratory or service provider that offers next-gen sequencing and deletion/duplication testing.
3. Follow the instructions provided by the laboratory for sample collection and submission.
4. Fill out the required forms and provide any relevant medical history or family history information.
5. Await the results from the laboratory and follow up with a healthcare provider for interpretation and guidance.

Who needs next-gen sequencing and deletionduplication?

1. Individuals with suspected genetic disorders or conditions that may be diagnosed through next-gen sequencing and deletion/duplication testing.
2. Patients with a family history of genetic diseases or conditions that may be inherited.
3. Healthcare providers looking to confirm a suspected genetic diagnosis or implement personalized treatment plans.

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What is next-gen sequencing and deletion/duplication?

Next-generation sequencing (NGS) is a technology used to sequence DNA and RNA quickly and cost-effectively. Deletion/duplication analysis is the process of identifying missing or duplicated sections of DNA.

Who is required to file next-gen sequencing and deletion/duplication?

Healthcare providers and laboratories are typically required to file next-gen sequencing and deletion/duplication reports.

How to fill out next-gen sequencing and deletion/duplication?

Next-gen sequencing and deletion/duplication reports are typically filled out by entering specific genetic information into a standardized form.

What is the purpose of next-gen sequencing and deletion/duplication?

The purpose of next-gen sequencing and deletion/duplication is to identify genetic variations that may be associated with certain medical conditions or diseases.

What information must be reported on next-gen sequencing and deletion/duplication?

Information such as gene mutations, copy number variations, and other genetic abnormalities must be reported on next-gen sequencing and deletion/duplication reports.