BME100 f2014:Group12 L6

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 COMPANY Peter Hillebrand Darci Botsch Devon Rusk Krishnaa Pradhan Sebastian Fonseca Jorge Espinoza LAB 6 WRITE-UP Bayesian Statistics Overview of the Original Diagnosis System What Bayes Statistics Imply about This Diagnostic Approach The Bayes values for calculations 1 and 2 were close to 100. From these values it can be inferred that the device is reliable. Based on these values a patient with a positive PCR result will most likely receive a positive final test conclusion, and a patient with a negative PCR result will most likely receive a negative final test conclusion. Sources of human error that could negatively effect the PCR include miscalculation and inaccurate measuring of the samples placed i the PCR machine. Machine error could include the failure of the machine to properly heat itself or track time, which would result in an error in the results used in calculating the Bayes Statistics. For calculations 3 and 4 the Bayes values were very small. These results imply that the PCR machine is reliable in predicting the development of the disease, or diagnosis. In other words, patients will most likely not receive a diagnosis prior to showing symptoms of the disease. Computer-Aided Design TinkerCAD The TinkerCad Tool is an online 3D design tool made for anyone to use in order to create designs. After learning how to use TinkerCAD, the provided PCR parts were imported into TinkerCAD and were placed together using the grouping tool. When each new part was imported, the piece was modified using the rotation tool in order for the parts to fit together correctly. The TinkerCAD tool made assembling the PCR parts together easy and allowed for modifications to the original PCR machine to be made because the parts were able to be modified in TinkerCAD. Our Design Feature 1: Consumables Kit The consumables were, for the most part, very well designed; they will be used similarly and packaged the same as they were in the PCR lab completed above. Although they worked very well, the consumables were not all flawless. For example, the fact that the primers were exclusive to specific nucleotides made them far less efficient than the ideal. A multi-platform primer is introduced in our design. Also addressed is the meticulous nature of the pipettor. The pipettes used necessitated extreme care and caution, and this made for an extremely slowed process. The improved pipettor is simpler and more refined for quick adjustment and use. One of the advantages of this new pipettor is that the amount of liquid it extracts can be modified and monitored through an electronic display window, and therefore the values can be entered by pressing the buttons with the digits that correspond to the desired value. Another of the improvements done in the consumable kits is the introduction of a mechanism to unload completely the substances that are taken in the pipettor. In several occasions this last device did not deliver 100% of the amount of the substance that it contained. Although the amount of liquid that remained is very small it could possibly contribute for errors in future experimental practices. Feature 2: Hardware - PCR Machine & Fluorimeter PCR Machine Our PCR Machine will be used in the same functional manner; it will test the samples and determine whether the patient is positive or negative in regards to the disease. There will, however, be improvements upon the previous design. The previous design was often defective, and this unreliability caused many issues including a great consumption of time as well as the losing of data. This must be rectified; every machine should work equally well, and every machine should be efficient in what it does. The time that is takes a PCR machine to execute its function has now been completely limited to two hours or less. Fluorimeter The fluorimeter's function will also remain unchanged. It will be used to measure the fluorescence in proportion to the total amount of substance measured. The fluorimeter used was not perfect; for example, one attribute that needs to be improved was the camera stand; whether a phone is used as the official camera or another more precise camera, the intended camera must be able to stay firmly in place; the picture should be taken from the same place every time to ensure consistency. This issue is addressed in our design; the camera stand is placed such that it does not have to be moved for any reason throughout the experiment. Another issue encountered was the precision aspect: a great deal of precision was necessary to complete the experiment, but the utensils given were not necessarily conducive to such results. What the fluorimeter needed was more instruments that allowed for precision; a set place to balance the pipette will be added to our fluorimeter to establish further consistency.