BME100 s2014:T Group1 L6: Difference between revisions

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{| style="wikitable" width="700px"
{| style="wikitable" width="700px"
|- valign="top"
|- valign="top"
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
| [[Image:Arianna2.jpg|150px|thumb|Name: Arianna Moreno]]
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
| [[Image:Pritish.jpg|150px|thumb|Name: Pritish Char]]
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
| [[Image:CJ.jpg|150px|thumb|Name: Chris Joseph Ibarra]]
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
| [[Image:JTS.jpg|150px|thumb|Name: Jared Smith]]
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
| [[Image:Hassam.jpg|150px|thumb|Name: Almoustafa Abbas]]
| [[Image:BME103student.jpg|100px|thumb|Name: student]]
|}
|}




''[Instructions: add the name of your team's company and/or product here]''
[[Image:MASIC_logo.png|400px]]




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'''TinkerCAD'''<br>
'''TinkerCAD'''<br>
TinkerCAD is a browser based 3D design tool. It allows for the creation of digital designs to be 3D printed into objects. We used the TinkerCad tool to design our improved PCR component. The changes were made to imporove the weakness found in the PCR machine.<br>


''[Instructions: A short summary (up to five sentences) of the TinkerCAD tool and how you used it in lab on November 20th]''<br>




'''Our Design'''<br>
'''Our Design'''<br>
[[Image: Group1Pcr_final.png]]


''[Instructions: Show an image of your TinkerCAD design here]''


''[Instructions: A short paragraph describing your design. Why did you choose this design? How is it different from the original OpenPCR design?]''<br>


The design we chose was primarily considered to make the PCR machine more convenient and less bulky. This allowed for the implementation of a bigger display  which allowed for more information about the processes going on to be shown on the bigger display (blue screen shown on tinkercad image). Also by using the "slide" implementation,it allows for the samples to be easily accessible when compared to the older design of the PCR machine(the gray tray is the sliding drawer). There are also rubber ends at the corners for durability and a handle on each side of the PCR for convenience. <br>


<br>
<br>
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==Feature 1: Disease SNP-Specific Primers==
==Feature 1: Disease SNP-Specific Primers==


''[Instructions: This information will come from the exercises you did in PCR Lab B.]''


'''Background on the disease-associated mutation'''<br>
'''Background on the disease-associated mutation'''<br>


''[Instructions: Use the answers from questions 3 - 7 to compose, in your own words, a paragraph about rs237025]''


SNP: a single nucleotide polymorphism , nucleotide is the basic building block of DNA, it is A compound consisting of a nucleotide lined to a phosphate group. polymorphism is a common variation in the DNA. SNP is when a single nucleotide differs from two different organisms of the same species. some SNP can have harmful effect on the organism which could causes diesease. genes related diseases such as cancer and diabetes. for example, rs237025; is a C/T variation in chromosome 6 in homosapians. it is linked to the hereditary disease known as diabetes type-1.




'''Primer design'''<br>
'''Primer design'''<br>


* Disease SNP-specific Forward Primer: ''[Instructions: type the sequence of the forward primer]''
* Disease SNP-specific Forward Primer: 5’  A  A  C  C  A  C  G  G  G  G  A  T  T  G  T  C  A  A  T  G
* Reverse Primer: ''[Instructions: type the sequence of the reverse primer]''
* Reverse Primer: 5’  A  G  T  T  T  T  C  T  A  A  T  T  G  A  G  A  A  T  G  C
 
How the primers work: ''[Instructions: explain what makes the primers disease-sequence specific. In other words, explain why the primers will amplify DNA that contains the disease-associated SNP, and will not exponentially amplify DNA that has the non-disease allele.]''
 


How the primers work:
Primers are complementary DNA sequence for DNA allele, they come in pair, one forward (complementary to the non coding strand) and the reverse primer (complementary to the coding strand). primers bond to the specified allele and the DNA polymerase replicate that specific allele and only that allele because the polymerase can only synthesize molecules with that primer.


<!-- Note: Be sure to delete the instruction text in brackets: ''[ ]'' -->
<!-- Note: Be sure to delete the instruction text in brackets: ''[ ]'' -->


==Feature 2: Consumables Kit==
==Feature 2: Consumables Kit==
'''Consumables Kit:'''
*Micropipette
*PCR Tubes
*SYBR Green I tubes
*Micropipette Tips
*Tube Tray
*Glass Slides


''[Instructions: Summarize how the consumables will be packaged in your kit. You may add a schematic image. An image is OPTIONAL and will not get bonus points, but it will make your report look awesome and easy to score.]''
<br>The MASICS Solutions Open PCR Machine will come with a preassembled consumables kit that contains labeled tubes, PCR mix solutions, primers and micropipettor tips. The items are plastic to ensure cost efficiency. To make every step easier for the user, our consumables kit is color coordinated for each item. Similarly, the tips will be separated (on opposite sides) of the solutions and primers to eliminate any confusion. The PCR also comes with a short and simple step-by-step tutorial displayed on our new display screen and can be looked at whenever necessary.
<br>The MASICS Solutions Open PCR Machine will come with a preassembled consumables kit that contains labeled tubes, PCR mix solutions, primers and micropipettor tips. The items are plastic to ensure cost efficiency. To make every step easier for the user, our consumables kit is color coordinated for each item. Similarly, the tips will be separated ( on opposite sides) of the solutions and primers to eliminate any confusion.
 
''[Instructions: IF your consumables packaging plan addresses any major weakness(es), explain how in an additional paragraph.]''


The problem we had with the consumables previously was that the pipette may have been taking inaccurate measurements because the twisting mechanism was not always precise, we decided that the current pipette was the best fit for our experiments and should not be addressed at this time.


<!-- Note: Be sure to delete the text in brackets: ''[ ]'' -->
<!-- Note: Be sure to delete the text in brackets: ''[ ]'' -->
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==Feature 3: Hardware - PCR Machine & Fluorimeter==
==Feature 3: Hardware - PCR Machine & Fluorimeter==


''[Instructions: Summarize how you will include the PCR machine and fluorimeter in your system. You may add a schematic image. An image is OPTIONAL and will not get bonus points, but it will make your report look really awesome and easy to score.]''
Our new design for the PCR machine is a convenient, less bulky design that allows for a bigger, touchscreen display. This way, the screen can display more information for the user to see and understand. We will be implementing a sliding method for the samples that increases the accessibility. The way this works is that the PCR will no longer have a lid but instead have a drawer for the samples that slides in an out of the PCR machine for the user to insert the tubes easily and accurately. In this sliding drawer, we made more holes for the sample tubes. We also made it so that it is much easier to access the inside by reducing the number of screws to remove. Now there are only six screws and once they are removed you can just slide the top right off. Also, for durability, we added rubber ends at the corners of the PCR to absorb any fall damage. Another key component of our machine is the larger base. The larger base allows more surface area for more tubes and faster heat transfer.
<br>
 
Our new design for the PCR machine is a convenient, less bulky design that allows for a bigger display screen. This way, the screen can display more information for the user to see and understand. We will be implementing a sliding method for the samples that increases the accessibility. The way this works is that the PCR will no longer have a lid but instead have a drawer for the samples that slides in an out of the PCR machine for the user to insert the tubes easily and accurately.
 
The new design for the Fluorimeter consists of a dark, 3D printed plastic design with a small door that simulates a "doggy-door" to take the picture using a smart phone. Because it is 3D printed, the stand and fluorimeter pieces are connected and able to be adjusted.
 
 
In our assessment of the original design, our group concluded that the Open PCR top was fragile. We felt that it may have been releasing some of the needed heat for the reaction and we wanted to eliminate this problem so that the reaction could possibly go faster. The machine was not very user friendly as it had a small screen and also only allowed for a few samples. With our new design we fixed this by adding more holes and by taking off the lid design, we were able to expand the screen and make it touch screen.  


In our assessment of the original design, our group concluded that the Open PCR top was fragile. We felt that it may have been releasing some of the needed heat for the reaction and we wanted to eliminate this problem without


''[Instructions: IF your group has decided to redesign the PCR machine and/or Fluorimeter to address any major weakness(es), explain how in an additional paragraph.]''
The fluorimeter's original design let in a lot of light but with our dark plastic 3D printed design, the material will not reflect light and also will not let light enter through any small holes like we had in the cardboard box mechanism. Another problem we had when taking photos was that the system would usually move when constantly lifting and putting down the box. Our design eliminates these problems and makes it easier for the user.




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==Bonus Opportunity: What Bayesian Stats Imply About The BME100 Diagnostic Approach==
==Bonus Opportunity: What Bayesian Stats Imply About The BME100 Diagnostic Approach==
''[Instructions: This section is OPTIONAL, and will get bonus points if answered thoroughly and correctly. Here is a chance to flex some intellectual muscle. In your own words, discuss what the results for calculations 3 and 4 imply about the reliability of PCR for predicting the disease. Please do NOT type the actual numerical values here. Just refer to them as being "close to one" or "very small." The instructors will ask you to submit your actual calculations via a Blackboard quiz. We are doing so for the sake of academic integrity and to curb any temptation to cheat.]''




The calculations seem to imply that the PCR is not terribly reliable for predicting positives, as the result of calculation three is much less than one. It is however, slightly more effective in predicting negatives, as the result of calculation four was relatively close to one. The results, in conjunction with one another, would imply that the PCR is not a very reliable way of predicting positive results, or negative results.


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Latest revision as of 10:00, 24 April 2014

BME 100 Spring 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: Arianna Moreno
Name: Pritish Char
Name: Chris Joseph Ibarra
Name: Jared Smith
Name: Almoustafa Abbas



LAB 6 WRITE-UP

Computer-Aided Design

TinkerCAD
TinkerCAD is a browser based 3D design tool. It allows for the creation of digital designs to be 3D printed into objects. We used the TinkerCad tool to design our improved PCR component. The changes were made to imporove the weakness found in the PCR machine.


Our Design


The design we chose was primarily considered to make the PCR machine more convenient and less bulky. This allowed for the implementation of a bigger display which allowed for more information about the processes going on to be shown on the bigger display (blue screen shown on tinkercad image). Also by using the "slide" implementation,it allows for the samples to be easily accessible when compared to the older design of the PCR machine(the gray tray is the sliding drawer). There are also rubber ends at the corners for durability and a handle on each side of the PCR for convenience.


Feature 1: Disease SNP-Specific Primers

Background on the disease-associated mutation


SNP: a single nucleotide polymorphism , nucleotide is the basic building block of DNA, it is A compound consisting of a nucleotide lined to a phosphate group. polymorphism is a common variation in the DNA. SNP is when a single nucleotide differs from two different organisms of the same species. some SNP can have harmful effect on the organism which could causes diesease. genes related diseases such as cancer and diabetes. for example, rs237025; is a C/T variation in chromosome 6 in homosapians. it is linked to the hereditary disease known as diabetes type-1.


Primer design

  • Disease SNP-specific Forward Primer: 5’ A A C C A C G G G G A T T G T C A A T G
  • Reverse Primer: 5’ A G T T T T C T A A T T G A G A A T G C

How the primers work: Primers are complementary DNA sequence for DNA allele, they come in pair, one forward (complementary to the non coding strand) and the reverse primer (complementary to the coding strand). primers bond to the specified allele and the DNA polymerase replicate that specific allele and only that allele because the polymerase can only synthesize molecules with that primer.


Feature 2: Consumables Kit

Consumables Kit:

  • Micropipette
  • PCR Tubes
  • SYBR Green I tubes
  • Micropipette Tips
  • Tube Tray
  • Glass Slides


The MASICS Solutions Open PCR Machine will come with a preassembled consumables kit that contains labeled tubes, PCR mix solutions, primers and micropipettor tips. The items are plastic to ensure cost efficiency. To make every step easier for the user, our consumables kit is color coordinated for each item. Similarly, the tips will be separated (on opposite sides) of the solutions and primers to eliminate any confusion. The PCR also comes with a short and simple step-by-step tutorial displayed on our new display screen and can be looked at whenever necessary.

The problem we had with the consumables previously was that the pipette may have been taking inaccurate measurements because the twisting mechanism was not always precise, we decided that the current pipette was the best fit for our experiments and should not be addressed at this time.


Feature 3: Hardware - PCR Machine & Fluorimeter

Our new design for the PCR machine is a convenient, less bulky design that allows for a bigger, touchscreen display. This way, the screen can display more information for the user to see and understand. We will be implementing a sliding method for the samples that increases the accessibility. The way this works is that the PCR will no longer have a lid but instead have a drawer for the samples that slides in an out of the PCR machine for the user to insert the tubes easily and accurately. In this sliding drawer, we made more holes for the sample tubes. We also made it so that it is much easier to access the inside by reducing the number of screws to remove. Now there are only six screws and once they are removed you can just slide the top right off. Also, for durability, we added rubber ends at the corners of the PCR to absorb any fall damage. Another key component of our machine is the larger base. The larger base allows more surface area for more tubes and faster heat transfer.


The new design for the Fluorimeter consists of a dark, 3D printed plastic design with a small door that simulates a "doggy-door" to take the picture using a smart phone. Because it is 3D printed, the stand and fluorimeter pieces are connected and able to be adjusted.


In our assessment of the original design, our group concluded that the Open PCR top was fragile. We felt that it may have been releasing some of the needed heat for the reaction and we wanted to eliminate this problem so that the reaction could possibly go faster. The machine was not very user friendly as it had a small screen and also only allowed for a few samples. With our new design we fixed this by adding more holes and by taking off the lid design, we were able to expand the screen and make it touch screen.


The fluorimeter's original design let in a lot of light but with our dark plastic 3D printed design, the material will not reflect light and also will not let light enter through any small holes like we had in the cardboard box mechanism. Another problem we had when taking photos was that the system would usually move when constantly lifting and putting down the box. Our design eliminates these problems and makes it easier for the user.


Bonus Opportunity: What Bayesian Stats Imply About The BME100 Diagnostic Approach

The calculations seem to imply that the PCR is not terribly reliable for predicting positives, as the result of calculation three is much less than one. It is however, slightly more effective in predicting negatives, as the result of calculation four was relatively close to one. The results, in conjunction with one another, would imply that the PCR is not a very reliable way of predicting positive results, or negative results.