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Department of Clinical Laboratory Genetics Genome Diagnostics Hereditary Disorders Toronto General Hospital Eaton Wing 11444, 200 Elizabeth Street Toronto, Ontario M5G 2C4 Director: Tracy Shockley,
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How to fill out genome diagnostics ampamp cancer
01
Gather all necessary information and documents regarding the patient's medical history, including family medical history.
02
Take a blood or tissue sample from the patient for analysis.
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Extract DNA from the sample and prepare it for sequencing.
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Use Next-Generation Sequencing (NGS) technology to read the patient's genome and identify any genetic variations or mutations.
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Analyze the genomic data using specialized software to interpret the results and identify potential cancer-related genetic variants.
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Compare the identified genetic variants with known cancer-related genetic markers and databases to determine their clinical significance.
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Follow up with the patient regularly to monitor any changes in their genomic profile and adjust the treatment plan if necessary.
Who needs genome diagnostics ampamp cancer?
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Individuals with a personal or family history of cancer who want to assess their genetic risk for developing cancer or identify potential hereditary cancer syndromes.
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Researchers and scientists studying the genetics of cancer or developing new treatments.
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Healthcare providers and oncologists who want to personalize patient care and treatment strategies based on genomic information.
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