BME103:T130 Group 14 - Revision history

Nathaniel Bennett: /* Research and Development */

2012-11-15T23:16:20Z

Research and Development

←Older revision		Revision as of 23:16, 15 November 2012
Line 213:		Line 213:

	'''Specific Cancer Marker Detection - The Underlying Technology'''<br><br>		'''Specific Cancer Marker Detection - The Underlying Technology'''<br><br>
-	'''Polymerase Chain Reaction'''	+	'''Polymerase Chain Reaction'''<br>
-	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>	+	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br>
-		+	[[Image:PCR_Group14.jpg\|400px]]<br>(Image taken from biology.kenyon.edu)<br><br>
	The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.		The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.
	<br><br>		<br><br>

Hope Haddad: /* Research and Development */

2012-11-15T21:27:44Z

Research and Development

←Older revision		Revision as of 21:27, 15 November 2012
Line 215:		Line 215:
	'''Polymerase Chain Reaction'''		'''Polymerase Chain Reaction'''
	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>		In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>
		+
	The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.		The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.
	<br><br>		<br><br>
	'''Bayes Rule'''<br>		'''Bayes Rule'''<br>
	[[Image:Bayes-rule.png\|200px]]<br>		[[Image:Bayes-rule.png\|200px]]<br>
-	The Bayes Theorem allows a scientist to interpret new data based on their expectations. The calculations show to false positives and inconsistencies in data. This is important in experiments such as the probability of a patient having cancer through a PCR testing such as this.	+	The Bayes Theorem allows a scientist to interpret new data based on their expectations. The calculations show to false positives and inconsistencies in data. This is important in experiments such as the probability of a patient having cancer through a PCR testing such as this. <br>
	Pr (A/B): Probability of a positive outcome		Pr (A/B): Probability of a positive outcome
	P (B/A): Probability of a true positive		P (B/A): Probability of a true positive

Hope Haddad: /* Research and Development */

2012-11-15T21:24:14Z

Research and Development

←Older revision		Revision as of 21:24, 15 November 2012
Line 218:		Line 218:
	<br><br>		<br><br>
	'''Bayes Rule'''<br>		'''Bayes Rule'''<br>
-	[[Image:Bayes-rule.png]]	+	[[Image:Bayes-rule.png\|200px]]<br>
		+	The Bayes Theorem allows a scientist to interpret new data based on their expectations. The calculations show to false positives and inconsistencies in data. This is important in experiments such as the probability of a patient having cancer through a PCR testing such as this.
		+	Pr (A/B): Probability of a positive outcome
		+	P (B/A): Probability of a true positive
		+	P (A): Chance of having the cancer
		+
		+
		+

Hope Haddad: /* Research and Development */

2012-11-15T21:13:56Z

Research and Development

←Older revision		Revision as of 21:13, 15 November 2012
Line 216:		Line 216:
	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>		In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>
	The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.		The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.
-	'''~~Process In Steps:~~'''	+	<br><br>
-	1. ~~Heat to 95 degrees Celsius for DNA polymerase~~	+	'''Bayes Rule'''<br>
-		+	[[Image:Bayes-rule.png]]
-		+

Hope Haddad: /* Research and Development */

2012-11-15T21:05:06Z

Research and Development

←Older revision		Revision as of 21:05, 15 November 2012
Line 213:		Line 213:

	'''Specific Cancer Marker Detection - The Underlying Technology'''<br><br>		'''Specific Cancer Marker Detection - The Underlying Technology'''<br><br>
-	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. In DNA replication, a bubble will form around a specific piece of DNA and divide, or unzip, the DNA. ~~From here~~ to <br><br>	+	'''Polymerase Chain Reaction'''
		+	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. Polymerase Chain Reaction(PCR) is used to determine a specific point on DNA that is to be copied. In DNA replication, a bubble of DNA primers and fluorescent tags will form around a specific piece of DNA and divide, or unzip (annealing) DNA. Any unneeded reagents in the solution will simply not bind to a base pair. In order for this to occur, the solution is heated to 95 degrees Celsius for about 3 minutes. Here, when the molecule is split into two, polymerase will add corresponding base pairs creating a first copy. For this to occur, the temperature needs to be brought down to about 57 degrees Celsius. At the same moment, polymerase is creating base pairs for the other half of the original DNA strand. The thermal cycler heats and cools the solution to complete the process. This process will cycle a few times in order to create duplicate DNA that is able to be tested for different reasons such as cancer. <br><br>
	The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.		The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.
		+	'''Process In Steps:'''
		+	1. Heat to 95 degrees Celsius for DNA polymerase
		+
		+

Hope Haddad: /* Research and Development */

2012-11-15T20:49:23Z

Research and Development

←Older revision		Revision as of 20:49, 15 November 2012
Line 212:		Line 212:
	==Research and Development==		==Research and Development==

-	'''Specific Cancer Marker Detection - The Underlying Technology'''<br>	+	'''Specific Cancer Marker Detection - The Underlying Technology'''<br><br>
-		+	In order to replicate DNA to work on, we must copy strands of DNA through a process called DNA replication. In DNA replication, a bubble will form around a specific piece of DNA and divide, or unzip, the DNA. From here to <br><br>
	The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.		The dye we added to each sample will fluoresce under UV light when DNA is present. If our eyesight was good enough, we would see that all the samples fluoresce slightly, however, because that is not the case, we do not. Instead, what we see fluoresce are samples that have a large amount of DNA present. We know from the experiment we created that we replicated cancerous DNA, specifically the r17879961 cancer associated sequence, meaning there would be excess amounts of the DNA in the sample if the patient has this cancerous sequence. Therefore, if a sample fluoresces bright enough for the naked eye to see, an excess amount of DNA is present and the patient does have cancer.

Hope Haddad: /* OUR TEAM */

2012-11-15T20:42:11Z

OUR TEAM

←Older revision		Revision as of 20:42, 15 November 2012
Line 16:		Line 16:
	\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]		\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
-	\| [[Image:~~BME103student~~.jpg\|100px\|thumb\|Name: ~~student~~<br>Role(s)]]	+	\| [[Image:Me_bme.jpg\|100px\|thumb\|Name: Hope Haddad<br>Role(s): Protocol/Research and Development Specialist]]
-	~~\| [[Image~~:~~BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)~~]]	+
-	~~\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]~~	+
	\|}		\|}

Hope Haddad: /* OUR TEAM */

2012-11-15T20:39:43Z

OUR TEAM

←Older revision		Revision as of 20:39, 15 November 2012
Line 14:		Line 14:
	\|- valign="top"		\|- valign="top"
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
-	\| [[Image:~~BME103student~~.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]	+	\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]		\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]

Hanna Rahman: /* OUR TEAM */

2012-11-15T19:07:06Z

OUR TEAM

←Older revision		Revision as of 19:07, 15 November 2012
Line 15:		Line 15:
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
-	\| [[Image:BME103_Group 14.JPG\|~~100px~~\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]	+	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[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)]]

Hanna Rahman: /* OUR TEAM */

2012-11-15T19:06:40Z

OUR TEAM

←Older revision		Revision as of 19:06, 15 November 2012
Line 15:		Line 15:
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
-	\| [[Image:BME103_Group 14.JPG\|~~25px~~\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]	+	\| [[Image:BME103_Group 14.JPG\|100px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[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)]]

←Older revision		Revision as of 20:42, 15 November 2012
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	\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]		\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
-	\| [[Image:~~BME103student~~.jpg\|100px\|thumb\|Name: ~~student~~<br>Role(s)]]	+	\| [[Image:Me_bme.jpg\|100px\|thumb\|Name: Hope Haddad<br>Role(s): Protocol/Research and Development Specialist]]
-	~~\| [[Image~~:~~BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)~~]]	+
-	~~\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]~~	+
	\|}		\|}

←Older revision		Revision as of 20:39, 15 November 2012
Line 14:		Line 14:
	\|- valign="top"		\|- valign="top"
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
-	\| [[Image:~~BME103student~~.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]	+	\| [[Image:Brianh.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]		\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: student<br>Role(s)]]

←Older revision		Revision as of 19:07, 15 November 2012
Line 15:		Line 15:
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
-	\| [[Image:BME103_Group 14.JPG\|~~100px~~\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]	+	\| [[Image:BME103_Group 14.JPG\|200px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[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)]]

←Older revision		Revision as of 19:06, 15 November 2012
Line 15:		Line 15:
	\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]		\| [[Image:Photo_on_11-14-12_at_9.37_PM.jpg\|120px\|thumb\|Name: Nathaniel Bennett<br>Role(s): PCR Technician/Research and Development Specialist]]
	\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]		\| [[Image:BME103student.jpg\|100px\|thumb\|Name: Brian Hedden<br>Roles: ImageJ Software Processor/Data Compiler & Analyzer]]
-	\| [[Image:BME103_Group 14.JPG\|~~25px~~\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]	+	\| [[Image:BME103_Group 14.JPG\|100px\|thumb\|Name: Hanna Rahman<br>Role: Protocol ]]
	\| [[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)]]