BME100 f2014:Group16 L6: Difference between revisions

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Revision as of 13:21, 19 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 COMPANY

Name: Christopher Saar
Protocol editer
Name: Gurpaul Sidhu
Role(s): Wiki editor, researcher
Picture Source:www. shadyrecords.com/wp-content/uploads/2013/01/royce.jpg
Name: student
Name: Sheania Morgan
image source: http://www.fandango.com/movie-photos/disney-takes-flight-from-dumbo-to-planes-886
Name: student
Name: Romann Arizmendi


LAB 6 WRITE-UP

Bayesian Statistics

Overview of the Original Diagnosis System

A The division of Labor
The PCR project was divided into wet-lab, lab procedure and data reclamation. These data point were labeled and sent to data analysis through ImageJ which was run at least 2 times for every data point. All data point were imported into excel for complete calculation and statistical analysis. The group was split three groups of two, wet lab and photo collection was acquired where three photos were collected for every data trial. All data trials were sent to the second group where ImageJ calculations were run twice and imported into excel. The third group was tasked to import the data into OpenWetWare and wiki coded to accurately and quick translate qualitative and quantitative data into tables and charts.


B Error Prevention


C PCR Results for the Class



What Bayes Statistics Imply about This Diagnostic Approach



Based upon the result of calculation 1 was extremely close to 100% which means that the PCR replicates are effective at concluding that a person has a disease SNP. Similarly, `the result of calculation 2 was also relatively high which means that if someone did not have the disease SNP the PCR replicates were efficacious in its conclusions. The first source of error was due to the fact that it was difficult to focus the camera which led to a certain degree of blurriness in the pictures. The second source of error was that there was no way to completely prevent light from entering the photo apparatus. The final error could have occurred due to the fact that he PCR reaction went past class time and therefore the DNA samples were forced to sit for an entire week.

The numerical value of calculation 3 was very low which means that the PCR is not effective at diagnosing or predicting the development of the disease. The same can be said about calculation 4 even though the value was slightly higher. The numerical value was not high enough for it to be claimed that the PCR reaction was effective at diagnosing the disease.

Computer-Aided Design

TinkerCAD


Our Design

TINKERCAD 1 TINKERCAD 2
TINKER CAD
TINKER CAD
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Feature 2: Consumables Kit

Feature 3: Hardware - PCR Machine & Fluorimeter