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Get the free Whole Exome Sequencing (WES) Reanalysis Request Form

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Nationwide Children's Laboratory Services Institute for Genomic Medicine (IGM) Clinical Laboratory 700 Children's Drive, Columbus, OH 43240 Phone: (614) 7223280 / FAX: (614) 7225471 Website: NationwideChildrens.org/LabWhole
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How to fill out whole exome sequencing wes

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How to fill out whole exome sequencing wes

01
Collect a blood or saliva sample from the individual who will undergo whole exome sequencing.
02
Send the sample to a laboratory that offers whole exome sequencing services.
03
The laboratory will extract DNA from the sample and prepare it for sequencing.
04
The exome, which contains all the protein-coding genes in the genome, will be sequenced using next-generation sequencing technology.
05
The sequenced data will be analyzed to identify any potential genetic variants or mutations that may be relevant to the individual's health.
06
A report will be generated summarizing the findings and providing recommendations for further medical evaluation or monitoring.

Who needs whole exome sequencing wes?

01
Individuals with suspected genetic disorders that cannot be diagnosed using traditional testing methods.
02
Individuals with a family history of genetic diseases or disorders.
03
Individuals with unexplained symptoms or medical conditions that may have a genetic basis.
04
Research laboratories conducting genetic studies or looking to identify novel disease-causing genes.
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Whole exome sequencing (WES) is a genomic technique that selectively sequences the protein-coding regions of genes in the genome.
Researchers, clinicians, or geneticists conducting genetic studies or diagnostic testing may be required to file whole exome sequencing (WES) data.
Whole exome sequencing (WES) data can be filled out using bioinformatics tools or software designed for analyzing and interpreting genetic data.
The purpose of whole exome sequencing (WES) is to identify genetic variations or mutations that may be associated with diseases or conditions.
Whole exome sequencing (WES) data typically includes information on genetic variants, gene mutations, and their potential impact on health.
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