BME103:TEMPwu2

From OpenWetWare

(Difference between revisions)
Jump to: navigation, search
(LAB 2 WRITE-UP)
Current revision (16:24, 16 November 2012) (view source)
(OUR TEAM)
 
(4 intermediate revisions not shown.)
Line 12: Line 12:
{| style="wikitable" width="700px"
{| style="wikitable" width="700px"
-
|-
+
|- valign="top"
| [[Image:BME103student.jpg|100px|thumb|Name: Student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Student<br>Role(s)]]
Line 28: Line 28:
-
'''Our Proposed Design'''<br>
+
'''System Design'''<br>
-
<!--- Add results from Week 3 exercise Part 2 --->
+
 
 +
 
 +
'''Key Features'''<br>
 +
 
 +
 
 +
 
 +
'''Instructions'''<br>
 +
 
 +
 
 +
<!--- From Week 4 exercise --->
Line 38: Line 47:
<!--- Design a new protocol based on your group's new PCR design. Make a step-by-step list of how someone should use your method
<!--- Design a new protocol based on your group's new PCR design. Make a step-by-step list of how someone should use your method
-
 
Things to consider:
Things to consider:
How should the PCR machine be set up? Does it need to be plugged in?
How should the PCR machine be set up? Does it need to be plugged in?
Line 50: Line 58:
--->
--->
-
'''Example List'''
+
'''Materials'''
-
# Step 1
+
 
-
# Step 2
+
<!--- Place your two tables "Supplied in the kit" and "Supplied by User" here --->
-
# Step 3
+
 
 +
 
 +
'''PCR Protocol'''
 +
 
 +
 
 +
 
 +
 
 +
'''DNA Measurement Protocol'''
 +
 
 +
 
==Research and Development==
==Research and Development==
-
<!--- Explain how PCR will be used to amplify signal from your target of choice and why the test will produce no signal if the target is absent --->
+
<!--- Bonus: explain how Bayesian statistics can be used to assess the reliability of your team's method. Just write the equation using variables that are relevant to your team's new test. You do not need actual numbers --->
 +
 
 +
 
 +
'''Background on Disease Markers'''
 +
 
 +
<!--- A description of the diseases and their associated SNP's (include the database reference number and web link) --->
 +
 
 +
 
 +
 
 +
 
 +
'''Primer Design'''
 +
 
 +
<!--- Include the sequences of your forward and reverse primers. Explain why a disease allele will give a PCR product and the non-disease allele will not. --->
 +
 
 +
 
-
<!--- Explain how Bayesian statistics can be used to assess the reliability of your team's method. Just write the equation using variables that are relevant to your team's new test. You do not need actual numbers --->
 
 +
'''Illustration'''
 +
<!--- Include an illustration that shows how your system's primers allow specific amplification of the disease-related SNP --->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
|}
|}

Current revision

BME 103 Fall 2012 Home
People
Lab Write-Up 1
Lab Write-Up 2
Lab Write-Up 3
Course Logistics For Instructors
Photos
Wiki Editing Help
Image:BME494_Asu_logo.png

Contents

OUR TEAM

Name: StudentRole(s)
Name: Student
Role(s)
Name: StudentRole(s)
Name: Student
Role(s)
Name: StudentRole(s)
Name: Student
Role(s)
Name: StudentRole(s)
Name: Student
Role(s)
Name: StudentRole(s)
Name: Student
Role(s)

LAB 2 WRITE-UP

Thermal Cycler Engineering

Our re-design is based upon the Open PCR system originally designed by Josh Perfetto and Tito Jankowski.


System Design


Key Features


Instructions





Protocols

Materials


PCR Protocol



DNA Measurement Protocol



Research and Development

Background on Disease Markers



Primer Design



Illustration


Personal tools