BME100 f2014:Group3 L6: Difference between revisions
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<!-- Instruction 1: In your own words, discuss what the results for calculations 3 and 4 imply about the reliability of PCR for *predicting the development disease* (referred to as "diagnosis"). Please do NOT type the actual numerical values here. Just refer to the Bayes values as being "close to 1.00 (100%)" or "very small." --> | <!-- Instruction 1: In your own words, discuss what the results for calculations 3 and 4 imply about the reliability of PCR for *predicting the development disease* (referred to as "diagnosis"). Please do NOT type the actual numerical values here. Just refer to the Bayes values as being "close to 1.00 (100%)" or "very small." --> | ||
Calculation 3: This shows how accurate the PCR machine is to predict the disease in a patient that would develop the disease. The test was not accurate given that it had a 43% efficiency rate. | |||
Calculation 4:This shows how accurate the PCR machine is to predict that a patient would not develop the disease. The test was even mess reliable than calculation 3 because it only showed a 27% efficiency rate. | |||
==Computer-Aided Design== | ==Computer-Aided Design== |
Revision as of 11:30, 20 November 2014
BME 100 Fall 2014 | Home People Lab Write-Up 1 | Lab Write-Up 2 | Lab Write-Up 3 Lab Write-Up 4 | Lab Write-Up 5 | Lab Write-Up 6 Course Logistics For Instructors Photos Wiki Editing Help | ||||||
OUR COMPANYLAB 6 WRITE-UPBayesian StatisticsOverview of the Original Diagnosis System
Calculation 2: This shows how accurate the test is to detect a negative result for SNP (specificity). The result for this test showed that the probability of a patent getting a negative result for having SNP from the PCR machine given that they do not have the disease is 77%. In other words, both of these show accuracy but also have room for improvement. This room for improvement comes from the error that occurred during the lab. These were a result from both human error and device error. Human errors include error in the preparation for the test. Specific tests that were shown to be positive should have displayed a negative result. This could be as a result from mixing up the samples. In the case for our group, the negative control (in other words, the sample that we knew should have displayed a negative result for the disease) displayed a positive result for SNP. The mix up in the samples probably occurred before we actually deceived the samples. This error could have also been a result of improper disposal of pipet tips before and after each use during preparation, thus causing a mix of samples. Device error includes not running the same amount of cycle in the open PCR machine. Each group's machine ran a different amount of cycles and some machines simply did not work at all. Receiving a positive result for our patient sample when it should have been negative left error in the Bayes values.
Calculation 4:This shows how accurate the PCR machine is to predict that a patient would not develop the disease. The test was even mess reliable than calculation 3 because it only showed a 27% efficiency rate. Computer-Aided DesignTinkerCAD The TinkerCAD tool is used just like the software SolidWorks, it is there to create 2-dimnsional or 3-dimensional figures online. TinkerCAD was used to make our 3-dimensional PCR. First we made all of the different pieces of the PCR separately and it was 2-dimensional. Then after all the separate pieces were made, it was put all together to make the final, 3-dimensional, product. Our Design
Feature 1: Consumables KitFeature 2: Hardware - PCR Machine & Fluorimeter |