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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 EXOME SEQUENCING (WES) REQUISITION PATIENT INFORMATION (COMPLETE
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How to fill out whole exome sequencing
How to fill out whole exome sequencing
01
Collect a blood or saliva sample from the individual to be tested.
02
Submit the sample to a laboratory that offers whole exome sequencing services.
03
The laboratory will isolate the DNA from the sample and prepare it for sequencing.
04
The exome, which represents the protein-coding regions of the genome, will be sequenced using high-throughput technology.
05
After sequencing is complete, bioinformatic analysis will be performed to identify any genetic variants or mutations within the exome.
06
The results will be interpreted by a genetic counselor or medical professional to determine any potential implications for the individual's health.
Who needs whole exome sequencing?
01
Individuals with suspected genetic disorders that have not been diagnosed through traditional testing methods.
02
Patients with a family history of genetic conditions or a known genetic mutation.
03
Individuals undergoing cancer treatment to identify targeted therapy options based on genetic mutations.
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What is whole exome sequencing?
Whole exome sequencing is a method for sequencing all the protein-coding regions in a genome.
Who is required to file whole exome sequencing?
Researchers, clinicians, and scientists may be required to file whole exome sequencing depending on the specific study or clinical situation.
How to fill out whole exome sequencing?
Whole exome sequencing data is typically analyzed using bioinformatics tools and software to identify genetic variants and their potential impact on health or disease.
What is the purpose of whole exome sequencing?
The purpose of whole exome sequencing is to identify genetic variants that may be associated with disease, traits, or other phenotypes.
What information must be reported on whole exome sequencing?
Information reported on whole exome sequencing may include genetic variants, gene mutations, and their potential implications for health.
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