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b/AWS/quizes/Chapter1_Quizes.json |
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[ |
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{ |
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"question": "Which of the following are quantitative biomarkers?", |
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"type": "many_choice", |
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"shuffle_answers": true, |
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"answers": [ |
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{ |
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"answer": "Inosine-5'-Monophosphate Dehydrogenase [IMPDH] Activity", |
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"correct": true, |
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"feedback": "Correct. IMPDH enzyme activity can be quantitatively measured." |
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}, |
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{ |
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"answer": "Association of Single Nucleotide Polymorphisms with Known Biomarkers of Alzheimer's Disease", |
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"correct": true, |
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"feedback": "Correct. The abundance of the SNP can be measured in the population and associated with AD through genome-wide association studies (GWAS)" |
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}, |
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{ |
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"answer": "Visual Observation of Potential Melanoma", |
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"correct": false, |
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"feedback": "Incorrect. Visual observation of potential skin cancer may suggest that additional tests are necessary." |
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}, |
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{ |
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"answer": "Single Cell Transcriptomics Analysis of Leukocytes", |
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"correct": true, |
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"feedback": "Correct. While specific transcriptomic biomarkers may be observed, the general pattern of transcription may also indicate a change in state." |
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}, |
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{ |
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"answer": "Discoloration of Eyes and Skin.", |
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"correct": false, |
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"feedback": "Incorrect. Chronic discoloration may indicate disease but are not themselves quantitative." |
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} |
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] |
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}, |
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{ |
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"question": "Which of the following biomarkers are part of a standard blood test?", |
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"type": "many_choice", |
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"shuffle_answers": true, |
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"answers": [ |
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{ |
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"answer": "High-Density/Low-Density Lipoproteins", |
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"correct": true, |
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"feedback": "Correct. HDL/LDL are the classic cholesterol biomarkers." |
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}, |
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{ |
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"answer": "Bilirubin", |
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"correct": true, |
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"feedback": "Correct. Bilirubin is an indicator of liver health." |
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}, |
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{ |
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"answer": "Tau Protein", |
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"correct": false, |
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"feedback": "Incorrect. Tau protein is a biomarker of Alzheimer's Disease but is not part of a standard blood test." |
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}, |
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{ |
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"answer": "Thyroid-Stimulating Hormone", |
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"correct": true, |
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"feedback": "Correct. Thyroid-stimulating hormone is an indicator of thyroid health." |
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}, |
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{ |
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"answer": "BRC1A Polymorphism rs799917", |
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"correct": false, |
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"feedback": "Incorrect. SNP's are not typically measured as part of a standard blood test except in specific cases." |
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}, |
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{ |
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"answer": "Platelets", |
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"correct": true, |
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"feedback": "Correct. The abundance of different types of blood cells are the primary biomarkers measured in a standard blood test." |
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} |
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] |
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}, |
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{ |
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"question": "Variations in the APOE gene can indicate a predisposition to Alzheimer's disease. Based on the BEST Glossary, what type(s) of biomarker is such a variant?", |
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"type": "many_choice", |
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"shuffle_answers": true, |
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"answers": [ |
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{ |
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"answer": "Susceptibility/Risk", |
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"correct": true, |
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"feedback": "Correct. APOE variants do not in and of themselves indicate the patient will get AD but they do indicate increased risk." |
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}, |
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{ |
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"answer": "Diagnostic", |
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"correct": false, |
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"feedback": "Incorrect. While APOE variants can be used for diagnosis, in this particular case, the disease has not yet developed." |
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}, |
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{ |
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"answer": "Monitoring", |
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"correct": false, |
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"feedback": "Incorrect. While the protein product of APOE (apolipiprotein E) could be used as a monitoring biomarker, the gene variants themselves will not change over the course of the disease." |
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}, |
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{ |
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"answer": "Prognostic", |
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"correct": true, |
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"feedback": "Correct. The specific variants present may indicate the severity of the AD that might develop." |
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}, |
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{ |
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"answer": "Predictive", |
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"correct": true, |
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"feedback": "Correct. The specific variant may indicate how a patient with the variant who develops AD might respond to a treatment compared to a patient without the variant." |
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}, |
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{ |
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"answer": "Response", |
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"correct": false, |
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"feedback": "Incorrect. The variant will not change in response to treatment and thus gives no indication on the effect of the treatment." |
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}, |
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{ |
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"answer": "Safety", |
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"correct": false, |
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"feedback": "Incorrect. The variant will not change in response to treatment and thus cannot indicate toxic effects of the treatment." |
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} |
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] |
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}, |
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{ |
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"question": "In a transcriptomics analysis of stomach cancer, you identify 30 genes that are significantly upregulated in cancer cells. Can these transcripts be used as clinical biomarkers?", |
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"type": "many_choice", |
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"shuffle_answers": true, |
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"answers": [ |
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{ |
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"answer": "Yes. The high correlation of the transcripts with disease states and low p-values indicate that they are good biomarkers.", |
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"correct": false, |
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"feedback": "Incorrect. While your assumption may turn out to be true, statistical significance and correlation are not definitive proof that the transcripts are directly related to the disease state." |
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}, |
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{ |
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"answer": "Yes. The transcripts are biologically relevant based on pathway analysis.", |
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"correct": false, |
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"feedback": "Incorrect. While the transcripts may be biological relevant, they may not be practical as biomarkers." |
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}, |
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{ |
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"answer": "No. The pathway analysis indicates no obvious biological rationale for the transcript expression.", |
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"correct": false, |
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"feedback": "Incorrect. Your assumption may be correct that the observed effect is an indirect correlation. However, you cannot rule out a novel direct effect without further verification." |
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}, |
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{ |
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"answer": "No. Transcripts are bad biomarkers.", |
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"correct": false, |
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"feedback": "Incorrect. A transcript is a perfectly valid biomarker, but as with any biomarker, its properties will determine its utility as a biomarker." |
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}, |
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{ |
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"answer": "Maybe. Additional experimental tests such as qPCR are necessary.", |
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"correct": true, |
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"feedback": "Correct. Biomarkers discovered through omics-based analysis should always be experimentally validated." |
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}, |
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{ |
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"answer": "Maybe. That's for the clinicians and engineers to figure out.", |
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"correct": true, |
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"feedback": "Correct. While your biomarkers may be statistically and biologically significant, a useful clinical biomarker must be practical in a clinical setting." |
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} |
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] |
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}, |
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] |