Difference between revisions of "Team:Mingdao/Model"

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<p>In our project, we want to calculate the bacteria concentration in the testers.  
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<p>In our project, we want to calculate the bacteria concentration in the testing devices.  
 
<p>
 
<p>
 
<p>
 
<p>
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<p>
 
<p>
 
<p>
 
<p>
What’s more, with the view to making sure our system works successfully, we need to make sure that testers can detect GFP in our devices. Since the GFP in mosquitoes take some time to be synthesized, we can detect the green fluorescence only few hours after the mosquitoes take in the tester’s blood. To prevent from the misleading of our devices and system, we should calculate the very beginning time that the testers can detect the green fluorescence in the devices.
+
What’s more, with the view to making sure our system works successfully, we need to make sure that GFP can be detected in our testing devices. Since the GFP in mosquitoes take some time to be synthesized, we can detect the green fluorescence only few hours after the mosquitoes take in the tester’s blood. To prevent from the misleading of our devices and system, we should calculate the very beginning time that the green fluorescence can be detected in the testing devices.  
 
</p>
 
</p>
 
<p>
 
<p>
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<p>
 
<p>
  
                 <p>Since our devices can only detect the GFP intensity, we can only utilize GFP intensity to calculate E.coli concentration. After obtaining E.coli concentration, we will utilize it to calculate the very beginning time that testers can detect GFP. Finally, the two parameters will be demonstrated on our devices for the testers to take as reference.  
+
                 <p>Since our devices can only detect the GFP intensity, we can only utilize GFP intensity to calculate E.coli concentration. After obtaining E.coli concentration, we will utilize it to calculate the very beginning time that GFP can be detected in the testing devices. Finally, the two parameters will be demonstrated on our devices for the testing devices to take as reference.
</p>
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<p>
 
<p>
 
<p>
 
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<p>
 
<p>
 
<p>
 
<p>
<p>To find the mathematical relationship between GFP and E.coli concentration, we measure the GFP growing curve with different MOI value every two hours. Then, perform a series of calculation and finally arrive at the mathematical relationship between GFP and E.coli concentration.</p>
+
<p>To find the mathematical relationship between GFP and E.coli concentration, we measure the GFP intensities with different MOI value every two hours. Then, perform a series of calculations and finally obtain the mathematical relationship between GFP intensity and E.coli concentration.</p>
 
<p>
 
<p>
 
<br />
 
<br />
 
<h3>Obtaining the Mathematical Relationship</h3>
 
<h3>Obtaining the Mathematical Relationship</h3>
 
<p>
 
<p>
<p>Table 1.0 shows the corresponding Fluorescence intensity with different MOI value. However, the units of E.coli we want should be transformed into another form.</p>
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<p>Table 1.0 shows the corresponding Fluorescence intensity with different MOI values. First of all, we transformed the MOI to E. coli density.</p>
 
<p>
 
<p>
 
<img class="center" src="https://static.igem.org/mediawiki/2018/f/fb/T--Mingdao--Modeling019.jpg"alt=" " style="width:35%" >
 
<img class="center" src="https://static.igem.org/mediawiki/2018/f/fb/T--Mingdao--Modeling019.jpg"alt=" " style="width:35%" >
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<img class="center" src="https://static.igem.org/mediawiki/2018/a/ac/T--Mingdao--Modeling03.jpg"alt=" " style="width:70%" >
 
<img class="center" src="https://static.igem.org/mediawiki/2018/a/ac/T--Mingdao--Modeling03.jpg"alt=" " style="width:70%" >
 
<p>
 
<p>
<p>Then, we will turn the MOI in Table 1.0 into E.coli density to form Table 1.1. Next, we will use Table 1.1 to keep figuring out the mathematical relationship between E.coli concentration and GFP intensity.</p>
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<pFinally, we turned the MOIs into E.coli density to form Table 1.1. In the following, we used Table 1.1 to calculate the mathematical relationship between E.coli concentration and GFP intensity.</p>
 
<br />
 
<br />
 
<h3>Forming the mathematical expression</h3>
 
<h3>Forming the mathematical expression</h3>
 
<p>
 
<p>
 
<p>
 
<p>
<p>Before we keep working on our calculation, it’s worth noticed that the GFP intensity has already existed while there is no E.coli . Thus, the intensity of GFP with no E.coli should be eliminated as discussing the relationship between E.coli concentration and GFP intensity, which means [GFP] should minus the [〖GFP〗_0] with no E.coli, and add it back in our final result.
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<p>The GFP intensity has background level in the existence of E.coli. Thus, the background intensity of GFP should be eliminated for the relationship between E.coli concentration and GFP intensity, which means [GFP] should minus the [〖GFP〗_0] in the presence of E.coli before DNA transfection (Table 1.2).
<p>
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With that in mind, we form the Table 1.2
 
With that in mind, we form the Table 1.2
 
<p>
 
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<p>
 
<p>
 
<p>
 
<p>
<p>With the formula, we can now build a calculator to calculate the [E.coli] by GFP Intensity, and apply the formula to our devices to from a well-designed prototype. The devices will calculate the [E.coli] automatically based on the GFP intensity they detect. As a result, the testers will be able to know the [E.coli] in their blood through our devices.</p>
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<p>With the formula, we can calculate the [E.coli] based on GFP Intensity, and apply the formula to our prototype design. </p>
<br />
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<h3>Limitation</h3>
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<p>
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<p>
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<p>However, there are some limitations to our Model 1. Not knowing when all the E.coli cells bind to the GAM 1 promoter, we can’t make sure when we can utilize the formula to conduct calculation.
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<p>
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Consequently, we will conduct Model 2 to figure out the limitation.</p>
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<p>
 
<p>
  
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<br />
 
<br />
<h2 id="d-model2">Model 2: Number of E.coli Cells Binding to The GAM 1 Promoter Increase With Time</h2>
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<h2 id="d-model2">Model 2: The GAM 1 Promoter in Response to Number of E. coli Cells Increase With Time</h2>
 
<br />
 
<br />
 
<h3>Method</h3>
 
<h3>Method</h3>
 
<p>
 
<p>
 
<p>
 
<p>
<p>To know when all the E.coli cells bind to GAM 1 promoter, we measure the GFP growing curves with different MOI value every two hours, and differentiate the growing curves to find the time that the instant GFP transcription rate reaches the maximum, which is the time all the E.coli cells bind to GAM 1 promoter.
+
<p>To know when GAM 1 promoter could be induced by E. coli concentration, we measure the GFP intensity with different MOI value every two hours, and differentiate the curves to find the time that the instant GFP expression level reaches the maximum, which is the time all the E.coli cells activate GAM 1 promoter.
<p>
+
After the differentiation, we will be able to obtain the graphic expression between the binding time and the [E.coli]. By analyzing the graphic expression, the very beginning time that the testers can detect GFP can be calculated.
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<p>
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In addition, the limitation mentioned in Model 1 can also be quantified via the graphic expression we obtained in Model 2.
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<p>
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</p>
 
</p>
 
<br />
 
<br />
<h3>Standardization of GFP Growing Curve</h3>
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<h3>Relative fluorescence units of GFP intensity in different MOIs of E. coli</h3>
 
<p>
 
<p>
 
<p>
 
<p>
<p>Since we need to differentiate the GFP growing curve, the standardization is essential. Thus, we will digitize the GFP growing curve so that we can conduct the differentiation successfully. </p>
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<p>The RFU of GFP intensities of GAM 1 promoter activities induced by different E.coli concentrations were shown in Table 2. </p>
<br />
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<h3>Raw Data</h3>
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<p>
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<p>
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<p>
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We perform two experiments respectively with different purposes.
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<p>
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The first one is to made for the blank so there is no DNA inside the well and no inducement of GAM 1 promoter, since the cells itself contribute to some absorbance, too.
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<p>
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The second one consists of E.coli with induced GAM 1 promoter. Both of the experiments are measured by our plate reader every two hours.
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<p>
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The Table 2.0 and Table 2.1 are shown below</p>
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<p>
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<img class="center" src="https://static.igem.org/mediawiki/2018/b/b2/T--Mingdao--Modeling11.jpg" alt=" " style="width:100%">
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<p>
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<img class="center" src="https://static.igem.org/mediawiki/2018/3/37/T--Mingdao--Modeling12.jpg" alt=" " style="width:100%">
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<br />
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<h3>Absorbance of green fluorescence protein</h3>
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<p>
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<p>
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<p>The actual absorbance of GFP is the absorbance of the E.coli cells with induced GAM 1 promoter minus the absorbance of E.coli cells without DNA and no inducement of GAM 1 promoter. After the calculation, the result are shown as Table 2.2</p>
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<p>
 
<p>
 
<img class="center" src="https://static.igem.org/mediawiki/2018/2/22/T--Mingdao--Modeling13.jpg" alt=" " style="width:100%">
 
<img class="center" src="https://static.igem.org/mediawiki/2018/2/22/T--Mingdao--Modeling13.jpg" alt=" " style="width:100%">
<br />
 
<h3>Standardization</h3>
 
<p>
 
<p>
 
<p>Then, we will illustrate the growing curves and find the formula of each growing curve so that we can differentiate them. It’s noticed that we don’t adopt the GFP growing curve without E.coli, since its GAM 1 promoter isn’t induced.
 
 
<p>
 
<p>
After analyzing, we find that cubic equation perfectly fits to our experiment data. Those cubic equations are shown as Figure 3.0 to Figure 3.4</p>
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<p>The RFU curves in the function of time were illustrated by different MOIs of E. coli, as shown from Figure 3.0 to Figure 3.4
 +
/p>
 
<p>
 
<p>
 
<img class="center" src="https://static.igem.org/mediawiki/2018/c/cb/T--Mingdao--Modeling002.jpg" alt=" " style="width:70%">
 
<img class="center" src="https://static.igem.org/mediawiki/2018/c/cb/T--Mingdao--Modeling002.jpg" alt=" " style="width:70%">
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<p>
 
<p>
 
<p>
 
<p>
<p>Also, the mathematical expressions of these cubic equations are shown as Table 3.0 and the graphic expressions are shown as Figure 4.0</p>
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<p>Also, the mathematical expressions of these cubic equations were shown as Table 3.0 and the graphic expressions were shown as Figure 4.0</p>
 
<p>
 
<p>
 
<p>
 
<p>
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<img class="center" src="https://static.igem.org/mediawiki/2018/4/46/T--Mingdao--Modeling008.jpg" alt=" " style="width:70%">
 
<img class="center" src="https://static.igem.org/mediawiki/2018/4/46/T--Mingdao--Modeling008.jpg" alt=" " style="width:70%">
 
<br />
 
<br />
<h3><strong>Number of E.coli Cells Binding to GAM 1 Promoter</strong></h3>
 
 
<br />
 
<br />
<h3>Derivative of the green fluorescence growing curve<h3>
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<h3>Derivative of the GFP Intensity Curve<h3>
<p>
+
 
<p>
 
<p>
<p>When all the E.coli cells bind to GAM 1 promoter, the instant GFP transcription rate will reach the maximum value. As a consequence, what we need to do is to differentiate the GFP growing curves at different MOI value, and find the maximum of the differentiated formulas as well as the corresponding time.
 
 
<p>
 
<p>
With that in mind, we conduct the derivative of the mathematical expressions in Table 3.0 and form Table 3.1
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<p>We conducted the derivative of the mathematical formula in Table 3.0 and form Table 3.1
 
</p>
 
</p>
 
<p>
 
<p>
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<img class="center" src="https://static.igem.org/mediawiki/2018/9/99/T--Mingdao--Modeling009.jpg" alt=" " style="width:70%">
 
<img class="center" src="https://static.igem.org/mediawiki/2018/9/99/T--Mingdao--Modeling009.jpg" alt=" " style="width:70%">
 
<br />
 
<br />
<h3>Obtaining The Maximum and The Corresponding Time</h3>
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<h3>The Responding Time to The Maximum of The Formula</h3>
 
<p>
 
<p>
 
<p>
 
<p>
<p>To calculate the maximum of the derivative of the green fluorescence growing curve, we need to conduct the second derivative and find the maximum and corresponding time. The result is shown as Table 3.2</p>
+
<p>To calculate the maximum of the derivative of the GFP intensity curve, we conducted the second derivative and found the maximum and responding time. The results were shown in Table 3.2</p>
 
<p>
 
<p>
 
<p>
 
<p>
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<p>
 
<p>
 
<p>
 
<p>
<p>Then, we will turn the MOI value into E.coli density to form Table 3.3
+
<p>The graphic expression of the relationship between time and E.coli density was shown in Table 3.3 and Figure 5.0</p>
Also, the graphic expression of the relationship between time and E.coli density is shown as Figure 5.0</p>
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<p>
 
<p>
 
<p>
 
<p>
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<p>
 
<p>
 
<p>
 
<p>
<p>With the formula, we can utilize the [E.coli] calculated in Model 1 to calculate how long the testers should wait to detect green fluorescence in our devices and demonstrate it on our devices to inform the testers. Then, the formula will also be applied to our calculator as well.</p>
+
<p>With the formula, we can use the [E.coli] to calculate the responding time. Then, the formula will also be applied to our calculator and prototype, too.</p>
 
<p>
 
<p>
 
<p>
 
<p>
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  <h2 id="d-conclusion">Conclusion</h2>
 
  <h2 id="d-conclusion">Conclusion</h2>
 
  <br />
 
  <br />
<p>Our model not only help to build the formulaic system which applied to our devices, but also make us better understand our project. Because our devices can only detect the GFP intensity, our model is required to build a well-designed devices and system.
+
<p>Our model not only help to build the mathematical system which applied to our devices, but also make us better understand our project. Because our devices can only detect the GFP intensity, our model is required to build a well-designed devices and system. In our model 1, we obtain the formula which allows us to calculate [E.coli] from GFP intensity. While in model 2, we obtain the formula which allows us to calculate how long the testing devices should wait to get the result of the test based on the [E.coli] calculated in mode 1. For [E.coli] and the time interval, they will be demonstrated on our devices to show them to the testing devices. To sum up, Our model act as a bridge between our devices and the testing devices, and quantifies the significant parameters in our project, which allow the masses to simply get the result of the test without complex calculations.</p>
In our model 1, we obtain the formula which allows us to calculate [E.coli] from GFP intensity. While in model 2, we obtain the formula which allows us to calculate how long the testers should wait to get the result of the test based on the [E.coli] calculated in mode 1. For [E.coli] and the time interval, they will be demonstrated on our devices to show them to the testers.  
+
To sum up, Our model act as a bridge between our devices and the testers, and quantifies the significant parameters in our project, which allow the masses to simply get the result of the test without complex calculations.</p>
+
  
  

Revision as of 06:53, 9 October 2018

Description

Modeling


Introduction


In our project, we want to calculate the bacteria concentration in the testing devices.

However, our devices can only detect GFP intensity, so we can only utilize GFP intensity to calculate bacteria concentration.

What’s more, with the view to making sure our system works successfully, we need to make sure that GFP can be detected in our testing devices. Since the GFP in mosquitoes take some time to be synthesized, we can detect the green fluorescence only few hours after the mosquitoes take in the tester’s blood. To prevent from the misleading of our devices and system, we should calculate the very beginning time that the green fluorescence can be detected in the testing devices.


Guiding Questions

1. How many bacteria can be tested in our model ? (Model 1)

2. How long do our devices take to send out signal ? (Model 2)


Focus on Our Model

Since our devices can only detect the GFP intensity, we can only utilize GFP intensity to calculate E.coli concentration. After obtaining E.coli concentration, we will utilize it to calculate the very beginning time that GFP can be detected in the testing devices. Finally, the two parameters will be demonstrated on our devices for the testing devices to take as reference.


Model 1: Calculating E.coli Concentration by GFP Intensity


Method

To find the mathematical relationship between GFP and E.coli concentration, we measure the GFP intensities with different MOI value every two hours. Then, perform a series of calculations and finally obtain the mathematical relationship between GFP intensity and E.coli concentration.


Obtaining the Mathematical Relationship

Table 1.0 shows the corresponding Fluorescence intensity with different MOI values. First of all, we transformed the MOI to E. coli density.


Conversion of MOI to E.coli density

The equation of E.coli density is shown below:

Since the MOI value refers to the ratio of E.coli cells to mosquito cells, we can use the density of mosquito cells to calculate the E.coli density. Plus, the mosquito cells are seeded at the density of 1.8×〖10〗^5 cells/well, and the volume of each well is 100μL.

Thus, the equation become


Forming the mathematical expression

The GFP intensity has background level in the existence of E.coli. Thus, the background intensity of GFP should be eliminated for the relationship between E.coli concentration and GFP intensity, which means [GFP] should minus the [〖GFP〗_0] in the presence of E.coli before DNA transfection (Table 1.2). With that in mind, we form the Table 1.2

Now we can begin with our data analyzing.


Data Analyzing

Figure 2.0 shows the graphic expression between the [E.coli] and GFP intensity, the Exponential Function is shown below:

Next, we will bring in that [〖GFP〗_0 ]=813 to the Exponential Function and obtain the final graphic expression and function.

Combining the constants, we arrive at


Conclusion


Application

With the formula, we can calculate the [E.coli] based on GFP Intensity, and apply the formula to our prototype design.


Model 2: The GAM 1 Promoter in Response to Number of E. coli Cells Increase With Time


Method

To know when GAM 1 promoter could be induced by E. coli concentration, we measure the GFP intensity with different MOI value every two hours, and differentiate the curves to find the time that the instant GFP expression level reaches the maximum, which is the time all the E.coli cells activate GAM 1 promoter.


Relative fluorescence units of GFP intensity in different MOIs of E. coli

The RFU of GFP intensities of GAM 1 promoter activities induced by different E.coli concentrations were shown in Table 2.

The RFU curves in the function of time were illustrated by different MOIs of E. coli, as shown from Figure 3.0 to Figure 3.4 /p>

Also, the mathematical expressions of these cubic equations were shown as Table 3.0 and the graphic expressions were shown as Figure 4.0



Derivative of the GFP Intensity Curve

We conducted the derivative of the mathematical formula in Table 3.0 and form Table 3.1


The Responding Time to The Maximum of The Formula

To calculate the maximum of the derivative of the GFP intensity curve, we conducted the second derivative and found the maximum and responding time. The results were shown in Table 3.2

The graphic expression of the relationship between time and E.coli density was shown in Table 3.3 and Figure 5.0

We also arrive at the equation between time and E.coli concentration


Conclusion


Application

With the formula, we can use the [E.coli] to calculate the responding time. Then, the formula will also be applied to our calculator and prototype, too.


CALCULATOR

E.coli Concentration Calculator

Type in the value:
The calculator can calculate E.coli density based on the GFP intensity.


Calculation Result
Variable Value Source
GFP Intensity     RFU
E.coli Concentration     Number of Cells Per uL Model 1

Responding Time Calculator

Enter value:
The calculator can calculate responding time based on the E.coli concentration.


Calculation Results
Variable Value Source
E.coli Density     Number of Cells Per uL
Responding Time       Hr Model 2

Conclusion


Our model not only help to build the mathematical system which applied to our devices, but also make us better understand our project. Because our devices can only detect the GFP intensity, our model is required to build a well-designed devices and system. In our model 1, we obtain the formula which allows us to calculate [E.coli] from GFP intensity. While in model 2, we obtain the formula which allows us to calculate how long the testing devices should wait to get the result of the test based on the [E.coli] calculated in mode 1. For [E.coli] and the time interval, they will be demonstrated on our devices to show them to the testing devices. To sum up, Our model act as a bridge between our devices and the testing devices, and quantifies the significant parameters in our project, which allow the masses to simply get the result of the test without complex calculations.

Introduction

Model 1

Model 2

Conclusion