History of Cancer Clinical Trial
Official title:
Personal Genomics: A Safety Study Assessing the Effects of Receiving Genome Sequencing Results
This study uses new methods called "genome sequencing" that allow the investigators to study
part or all of a person's genome. The genome is the collection of all of a person's genes.
Genes carry the instructions that our bodies need to develop and function. Genes are passed
on from one generation to the next. Genome sequencing can study all of a person's genome
(whole genome sequencing) or just parts of their genome (whole exome sequencing). In the
study, the investigators refer to all these research methods as 'genome sequencing'. Genome
sequencing typically shows a large number of gene changes, known as "variants." Some (but not
all) of these genetic variants may be linked to increased risks of diseases other than
cancer.
The purpose of this study is to learn what kinds of genetic variants the patient wants to
learn about from their genome.
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Status | Clinical Trial | Phase | |
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Recruiting |
NCT05162846 -
Methods for Increasing Genetic Testing Uptake in Michigan
|
N/A |