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Edinburgh Research Explorer A genome wide association study links glutamate receptor pathway to Sporadic Creutzfeldt-Jakob disease risk. Citation for published version: Sanchez Juan, P, Bishop, M,
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How to fill out a genome wide association

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Collect a large sample size of individuals with and without the trait of interest.
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Genotype each individual at hundreds of thousands to millions of genetic variants.
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Analyze the genotype data to identify genetic variants that are associated with the trait of interest.
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Validate the findings in independent samples to confirm the associations.

Who needs a genome wide association?

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Researchers studying the genetic basis of complex traits or diseases.
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Medical professionals looking to identify genetic risk factors in patients.
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Pharmaceutical companies developing personalized medicine treatments.
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A genome wide association study (GWAS) is a research approach used to identify genetic variants associated with specific traits or diseases by scanning the genome of many individuals.
Researchers conducting GWAS to investigate associations between genetic variants and traits or diseases are typically required to file a genome wide association report.
Filling out a genome wide association report generally involves inputting data regarding genetic variants, sample populations, statistical methods, and findings into a standardized format or database.
The purpose of a genome wide association is to identify and understand the genetic underpinnings of diseases or traits, which can lead to better diagnosis, treatment, and prevention strategies.
Information that must be reported typically includes study design, participant demographics, genetic variants analyzed, statistical results, and implications of the findings.
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