Molecular diagnosis in microbiology involves identifying microorganisms (such as bacteria, viruses, or fungi) based on their genetic material, such as DNA or RNA, rather than their physical characteristics. This technique allows for faster and more accurate identification of pathogens compared to traditional methods that rely on culturing, making it particularly useful for detecting difficult-to-grow or fastidious organisms. Common molecular techniques used include polymerase chain reaction (PCR), nucleic acid hybridization, and sequencing.
Definitive diagnosis of viral hemorrhagic fever rests on laboratory testing, including molecular techniques like PCR to detect viral genetic material, serologic tests to measure antibodies produced by the immune system in response to the virus, and viral isolation in cell culture. Clinical symptoms and epidemiological factors can also be important in making a diagnosis of viral hemorrhagic fever.
One of the newest ways to analyze cells and diagnose illnesses is called molecular imaging. Molecular imaging can be used to help people with breast cancer because it provides detailed images of what's going on inside the body.
To really understand this process, consider the idea that nucleic acid combinations are like keys, and diagnoses are like locks. When you arrange the different acids (A, C, T, U), you are essentially creating a new key. This tells the body that THAT key will fit in THIS lock, meaning that the diagnosis will then fit the conditions of the lock. The sequences match up to the conditions of the diagnosis.
Molecular Gastronomy
Molecular
Michael J. Murphy has written: 'Molecular diagnostics in dermatology and dermatopathology' -- subject(s): Genetics, Methods, Molecular diagnosis, Skin Diseases, Molecular Diagnostic Techniques, Diagnosis, Skin, Pathology, Diseases
Diagnosis is achieved first by a clinical diagnosis from a clinical geneticist, followed by molecular genetic testing in a CLIA-approved diagnostic laboratory
Lela Buckingham has written: 'Molecular diagnostics' -- subject(s): Nucleic Acids, Molecular diagnosis, Molecular Diagnostic Techniques, Methods, Analysis
Molecular Data: Information such as DNA sequences, levels of genetic expression, biomarkers and protein structure and function that are key to modern cancer research, diagnosis and treatment.
Domnita Crisan has written: 'Hematopathology' -- subject(s): Genetics, Diseases, Hematologic diseases, Molecular aspects, Molecular Pathology, Genetic aspects, Diagnosis, Pathology, Blood
Patients with Kennedy's disease usually receive a definitive diagnosis in a clinical molecular genetics laboratory. This requires DNA extraction from blood, followed by testing the gene that causes Kennedy's disease
Myotonic dystrophy is diagnosed clinically in individuals that have a specific type of muscle weakness. This is confirmed with molecular genetics testing, where the DMPK is analyzed
Definitive diagnosis of viral hemorrhagic fever rests on laboratory testing, including molecular techniques like PCR to detect viral genetic material, serologic tests to measure antibodies produced by the immune system in response to the virus, and viral isolation in cell culture. Clinical symptoms and epidemiological factors can also be important in making a diagnosis of viral hemorrhagic fever.
One of the newest ways to analyze cells and diagnose illnesses is called molecular imaging. Molecular imaging can be used to help people with breast cancer because it provides detailed images of what's going on inside the body.
Matteo Adinolfi has written: 'Non-isotopic in situ hybridization' -- subject(s): DNA, Diagnosis, Diagnostic use, Genetic disorders, In situ hybridization, Molecular biology
A diagnosis of mitochondrial myopathies is confirmed through a combination of clinical evaluation, muscle biopsy to look for mitochondrial abnormalities, and genetic testing to identify mutations in mitochondrial DNA or nuclear DNA. Additional tests may also be conducted to assess muscle function and metabolic abnormalities.
To really understand this process, consider the idea that nucleic acid combinations are like keys, and diagnoses are like locks. When you arrange the different acids (A, C, T, U), you are essentially creating a new key. This tells the body that THAT key will fit in THIS lock, meaning that the diagnosis will then fit the conditions of the lock. The sequences match up to the conditions of the diagnosis.