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Molecular Diagnostics Laboratory Molecular Diagnostics Laboratory

Molecular Diagnostics Laboratory - PowerPoint Presentation

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Uploaded On 2020-06-17

Molecular Diagnostics Laboratory - PPT Presentation

Department of Pathology and Laboratory Medicine Molecular Team Top Dr Paul Rothberg Bonnie Nuccie Middle Sharon Todd Nufatt Paige Bottom Suni Yanyun Bill John What is Molecular Diagnostics ID: 780156

dna molecular determine diagnostics molecular dna diagnostics determine marrow genetic bone pcr transplant post testing blood cells risk patients

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Slide1

Molecular Diagnostics LaboratoryDepartment of Pathology and Laboratory Medicine

Molecular Team

Top: Dr. Paul Rothberg, Bonnie

Nuccie

Middle: Sharon, Todd,

Nufatt

, Paige

Bottom:

Suni

,

Yanyun

, Bill, John

What is Molecular Diagnostics?

Molecular diagnostic testing is used to diagnose and

monitor oncological and genetic diseases. It helps determine

risk and prognosis.

By

analyzing the individual's genetic code and how their cells express their genes as proteins, molecular diagnostics allows for personalized medicine .

How Is DNA Analyzed?

DNA is first extracted from the blood, bone marrow, or tissue samples. The polymerase

chain reaction (PCR

) is the technique used for the amplification of DNA to make millions of replicates of a target DNA sequence. Specific mutations which can be associated with certain diseases are detected once

the DNA is

amplified.

H

ow Do We Help Our Patients?

Bone Marrow Transplants: Molecular diagnostics plays a large role in stem cell transplants by determining whose cells are populating the bone marrow post transplant (donor or recipient?) This difference helps the treatment team determine the next steps for a successful transplant. Oncology: Molecular testing can diagnose and help guide therapy for patients with all varieties of cancer (lung, colon, brain, skin, blood, etc.)Genetics: There are certain genetic mutations that are risk factors for bleeding and iron overload disorders. Molecular diagnostics can help determine if the patient has the mutation and the likelihood the patient will develop the disease.

DNA sequencing analysis

Post PCR gel electrophoresis

Real time PCR of the

KRAS

gene