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BAYLOR GENETICS 2450 HOLCOMBE BLVD. GRAND BLVD. RECEIVING DOCK HOUSTON, TX 770212024PHONE 1.800.411.4363 FAX 1.800.434.9850CONNECTWHOLE GENOME SEQUENCING (WGS) REQUISITION PATIENT INFORMATION (COMPLETE

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How to fill out whole genome sequencing test

01

Choose a reputable laboratory or provider for the test.

02

Obtain a prescription or request from a healthcare professional.

03

Provide a DNA sample usually through a blood sample or saliva collection.

04

Wait for the results and consult with a genetic counselor or healthcare provider.

Who needs whole genome sequencing test?

01

Individuals with a family history of genetic conditions or diseases.

02

Patients with undiagnosed medical conditions or rare disorders.

03

Couples planning to have children who want to assess genetic risks.

04

Those interested in personalized medicine or pharmacogenomics.

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What is whole genome sequencing test?

Whole genome sequencing test is a laboratory method that determines the complete DNA sequence of an organism's genome at a single time.

Who is required to file whole genome sequencing test?

Individuals or entities seeking to analyze DNA for medical, research, or genealogical purposes may be required to file a whole genome sequencing test, depending on specific regulations and guidelines.

How to fill out whole genome sequencing test?

To fill out a whole genome sequencing test, one must typically provide personal information, consent for testing, and any specific details regarding the purpose of the test, alongside sample submission forms as required by the testing laboratory.

What is the purpose of whole genome sequencing test?

The purpose of whole genome sequencing test is to identify genetic variations that may contribute to diseases, inform treatment options, and enhance understanding of an individual's genetic makeup.

What information must be reported on whole genome sequencing test?

Information that must be reported includes the sequencing results, interpretation of genetic variants, potential health implications, and any relevant family history or data used in the analysis.

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