Team:TCU Taiwan/Modeling
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<li><a href="#" style="cursor:default"><font size="5">Team</font></a> | <li><a href="#" style="cursor:default"><font size="5">Team</font></a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Team"><font size="3"> | + | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Team"><font size="3">Members</font></a></li> |
+ | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Achievements"><font size="3">Achievements</font></a></li> | ||
<li><a href="https://igem.org/Team.cgi?id=1473" target="_blank"><font size="3">Official Team Profile</font></a></li> | <li><a href="https://igem.org/Team.cgi?id=1473" target="_blank"><font size="3">Official Team Profile</font></a></li> | ||
<li><a href="https://2014.igem.org/Team:TCU_Taiwan/Contact"><font size="3">Contact</font></a></li> | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Contact"><font size="3">Contact</font></a></li> | ||
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<li><a href="#" style="cursor:default"><font size="5">Project</font></a> | <li><a href="#" style="cursor:default"><font size="5">Project</font></a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Project"><font size="3"> | + | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Project"><font size="3">Introduction</font></a></li> |
<li><a href="https://2014.igem.org/Team:TCU_Taiwan/Parts"><font size="3">Parts</font></a></li> | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/Parts"><font size="3">Parts</font></a></li> | ||
<li><a href="https://2014.igem.org/Team:TCU_Taiwan/SystemDesign"><font size="3">System Design</font></a></li> | <li><a href="https://2014.igem.org/Team:TCU_Taiwan/SystemDesign"><font size="3">System Design</font></a></li> | ||
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<legend class="qnum" align="center"><font face="Trebuchet MS" size="6" color="#0092C7">1.Introduction</font><br> | <legend class="qnum" align="center"><font face="Trebuchet MS" size="6" color="#0092C7">1.Introduction</font><br> | ||
<font size="3" face="Verdana" color="#333"></font></legend> | <font size="3" face="Verdana" color="#333"></font></legend> | ||
- | <div class="wrapper" style="background-color: white;"><font size="3" face="Verdana" color="#333"> | + | <div class="wrapper" style="background-color: white;"> |
+ | <font size="3" face="Verdana" color="#333"><p>Because our Trogene Horse use phages as vector, it is very important to know how to make the best of these phages. This means we need to get a condition under which these phages can work most efficiently. <br><br> | ||
+ | In our experiment, the phage display can be descripted as:<br> | ||
+ | Prepare <em>E.coli</em> JM101 with phagemid→ Add M13KO7 to infect JM101 → Add kanamycin for selection → Incubate for phagemid-carrying phage releasing → Use phagemid-carrying phage infect blank JM101.<br><br> | ||
+ | Thus, we chose two events as characters of phage’s efficiency:<br> | ||
+ | </p> | ||
+ | <p>1. The release amount of phage after helper phage infection.<br> | ||
+ | 2. The infection rate of our phagemid-carrying phage<br> | ||
+ | </p> | ||
+ | <p>So we collected some experimental data for modeling. And here comes the result.<br> | ||
+ | We wolud like to give our appreciation to NCTU-Formosa, they taught us how to make this modeling.</p> | ||
+ | </font> | ||
+ | |||
+ | |||
+ | |||
+ | </div> | ||
<br> | <br> | ||
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<fieldset> | <fieldset> | ||
- | <legend class="qnum" align="center"><br> | + | <legend class="qnum" align="center"><font face="Trebuchet MS" size="6" color="#0092C7">3.Building the Model</font><br> |
<font size="3" face="Verdana" color="#333"></font></legend> | <font size="3" face="Verdana" color="#333"></font></legend> | ||
- | <div class="wrapper" style="background-color: white;"><font size="3" face="Verdana" color="#333"> | + | <div class="wrapper" style="background-color: white;"> |
+ | <p><font color="#333" size="3" face="Verdana">To build the model,we created, trained, and tested <strong>A</strong>daptive <strong>N</strong>etwork-based <strong>F</strong>uzzy <strong>I</strong>nference <strong>S</strong>ystem | ||
+ | (ANFIS).We performed the following tasks:</font></p> | ||
+ | <p><font color="#333" size="3" face="Verdana">1.Data <a href="http://en.wikipedia.org/wiki/Data_pre-processing" target="_blank">pre-processing</a><br> | ||
+ | 2.Loading the Data<br> | ||
+ | 3.Generating the Initial ANFIS Structure<br> | ||
+ | 4.Training the ANFIS<br> | ||
+ | 5.Validating the Trained ANFIS</font></p><font size="3" face="Verdana" color="#333"> | ||
+ | <font face="Trebuchet MS" size="5" color="#90B849"><p> </p> | ||
+ | <p>1.Data pre-processing</p> | ||
+ | </font> | ||
+ | |||
+ | <p>We generated 70 data from our experiment and then picked $1\over 5$ of them randomly as Training Data. The other $4\over 5$ is treated as Testing Data.</p> | ||
+ | |||
+ | <p>Because our results are too large (at least 10<sup>8</sup>), we divided them by 1 x 10<sup>6</sup>. This can help us analyzed these results more quickly.</p><font size="3" face="Verdana" color="#333"><font face="Trebuchet MS" size="5" color="#90B849"> | ||
+ | <p>2.Loading the Data</p> | ||
+ | </font> | ||
+ | </font> | ||
+ | <p>To train the ANFIS, we must begin by loading a Training data set that contains the desired input/output data of the system to be modeled. Any data set we load must be an array with the data arranged as column vectors, and the output data in the last column.We also loaded Testing data.</p> | ||
+ | <p> </p> | ||
+ | <p><font face="Trebuchet MS" size="5" color="#90B849">3.Generating the Initial ANFIS Structure</font></p> | ||
+ | </font> | ||
+ | <p><font color="#333" size="3" face="Verdana">Before we start the ANFIS training, we specify an initial ANFIS model structure as below:</font></p> | ||
+ | <p> </p> | ||
+ | <table width="70%" border="0" cellspacing="0" cellpadding="0" align="center"> | ||
+ | <tr> | ||
+ | <td align="center"><img src="https://static.igem.org/mediawiki/2014/8/8c/TCU_MD_Structure.png" width="100%"></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td align="center"><font size="3" face="Verdana"><strong>Fig3.1 Initial ANFIS Model Structure</strong></font></td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <font color="#333" size="3" face="Verdana"> | ||
+ | <p>The branches in this graph are color coded. Color coding of branches characterize the rules and indicate whether or not<em> and</em>, <em>not</em>, or <em>or</em> are used in the rules. The input is represented by the left-most node and the output by the right-most node. The node represents a normalization factor for the rules. </p></font> | ||
+ | <p> </p> | ||
+ | <p><font face="Trebuchet MS" size="5" color="#90B849">4.Training the ANFIS</font></p> | ||
+ | <p><font color="#333" size="3" face="Verdana">After loading the training data and generating the initial ANFIS structure, we started training the ANFIS. The number of training Epochs(Epochs means number of iterations) is over 2500.</font></p> | ||
+ | <p><font color="#333" size="3" face="Verdana">During training we can see how Training error develops as below:</font><br><br> | ||
+ | <p> | ||
+ | <table width="85%" border="0" cellspacing="0" cellpadding="0" align="center"> | ||
+ | <tr> | ||
+ | <td align="center"><img src="https://static.igem.org/mediawiki/2014/d/dd/TCU_MD_Training_error.png" width="100%"></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td align="center"><font size="3" face="Verdana"><strong>Fig3.2 Training Error</strong></font></td> | ||
+ | </tr> | ||
+ | </table></p> | ||
+ | <p> </p> | ||
+ | <p><font face="Trebuchet MS" size="5" color="#90B849">5.Validating the Trained ANFIS</font></p> | ||
+ | <p><font color="#333" size="3" face="Verdana">Finally,we had to test our data against the trained ANFIS.After the ANFIS is trained, validate the model using a Testing data that differs from the one we used to train the ANFIS. </font></p> | ||
+ | <p><font color="#333" size="3" face="Verdana">When we test the testing data against the ANFIS, it looks satisfactory.</font></p> | ||
+ | <p> </p> | ||
+ | <table width="85%" border="0" cellspacing="0" cellpadding="0" align="center"> | ||
+ | <tr> | ||
+ | <td align="center"><img src="https://static.igem.org/mediawiki/2014/e/e1/TCU_MD_Test.png" width="100%"></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td align="center"><font size="3" face="Verdana"><strong>Fig3.3 Testing our data against the trained ANFIS</strong></font></td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
+ | |||
+ | |||
+ | </font> | ||
+ | </div> | ||
<br> | <br> | ||
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<legend class="qnum" align="center"><font face="Trebuchet MS" size="6" color="#0092C7">4.</font><font face="Trebuchet MS" size="6" color="#0092C7">Results</font><br> | <legend class="qnum" align="center"><font face="Trebuchet MS" size="6" color="#0092C7">4.</font><font face="Trebuchet MS" size="6" color="#0092C7">Results</font><br> | ||
<font size="3" face="Verdana" color="#333"></font></legend> | <font size="3" face="Verdana" color="#333"></font></legend> | ||
- | <div class="wrapper" style="background-color: white;"> | + | <div class="wrapper" style="background-color: white;"><br> |
- | <p><font size="3" face="Verdana" color="#333">We chose two variables to find the best release amount of phage after helper phage infecting. The first variable is the time after we input helper phages M13KO7 into <em>E. | + | <p><font face="Trebuchet MS" size="5" color="#90B849">Model 1 : Release</font> </p><p><font size="3" face="Verdana" color="#333">We chose two variables to find the best release amount of phage after helper phage infecting. The first variable is the time after we input helper phages M13KO7 into <em>E.coli </em>(JM101) with phagemid pBluescript II SK(-).(We have put<a href="http://parts.igem.org/Part:BBa_I13521" target="_blank"> BBa_I13521</a> inside as an reporter gene.)This is the time for helper phages to infect bacterium.<br><br> |
After the infection, we added kanamycin into these JM101 for selection becauseJM101 can get kanamycin resistance only when they are infected by M13KO7. Then we incubated these JM101 so they can have time to release phagemid-carrying phage, and the incubating time is the second variable in our test.<br><br> | After the infection, we added kanamycin into these JM101 for selection becauseJM101 can get kanamycin resistance only when they are infected by M13KO7. Then we incubated these JM101 so they can have time to release phagemid-carrying phage, and the incubating time is the second variable in our test.<br><br> | ||
- | As we can see in this figure, the most amount of phage being released is at the time when we add kanamycin after 30 minutes of infection and then incubate them for 14 hours. Under this condition, the best releasing amount of phage is 4×10 | + | As we can see in this figure, the most amount of phage being released is at the time when we add kanamycin after 30 minutes of infection and then incubate them for 14 hours. Under this condition, the best releasing amount of phage is 4×10<sup>10</sup> pfu/ml.</font></p> |
- | <table width="80%" border=" | + | <font size="3" face="Verdana" color="#333"><p>This modleing is been helper by NCTU-Formosa. They analyzed our data and made this modeling.</p></font> |
- | + | <font size="3" face="Verdana" color="#333"><p>Thanks NCTU-Formosa!!! You are our best friend!<br> | |
+ | <br> | ||
+ | </p></font> | ||
+ | <table width="80%" border="0" cellspacing="0" cellpadding="0" align="center"> | ||
+ | <tr> | ||
<td align="center"><img src="https://static.igem.org/mediawiki/2014/d/d8/TCU_MD_Surface1.jpg" width="837" height="421"></td> | <td align="center"><img src="https://static.igem.org/mediawiki/2014/d/d8/TCU_MD_Surface1.jpg" width="837" height="421"></td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td align="center"><font size="3" face="Verdana"><strong> | + | <td align="center"><font size="3" face="Verdana"><strong>Fig4.1 Model1</strong></font></td> |
</tr> | </tr> | ||
- | + | </table> | |
<p> </p> | <p> </p> | ||
- | <br><br><br> | + | <p> </p> |
+ | <br><br> | ||
+ | <font face="Trebuchet MS" size="5" color="#90B849">Model 2 : Infection Rate</font><br> | ||
<font size="3" face="Verdana" color="#333"><p>Then we came up with another question: Under which condition will we get the best infection rate of our phagemid-carrying phage? We believe this is influenced by the MOI between phages and bacterium. MOI means multiplicity of infection, it is the ratio of agents (phage-carrying phage) to infection targets (<em>E.coli</em> JM101). So we choose MOI as the variable, and incubate bacterium for 1 hour after infecting.<br> | <font size="3" face="Verdana" color="#333"><p>Then we came up with another question: Under which condition will we get the best infection rate of our phagemid-carrying phage? We believe this is influenced by the MOI between phages and bacterium. MOI means multiplicity of infection, it is the ratio of agents (phage-carrying phage) to infection targets (<em>E.coli</em> JM101). So we choose MOI as the variable, and incubate bacterium for 1 hour after infecting.<br> | ||
- | In our test, we found that as long as the MOI is higher than 6 pfu/cfu, the infection rate can access 100%. This is an exciting result!!</p></font | + | In our test, we found that as long as the MOI is higher than 6 pfu/cfu, the infection rate can access 100%. This is an exciting result!!</p></font><br><br> |
- | <table width="70%" border=" | + | <table width="70%" border="0" cellspacing="0" cellpadding="0" align="center"> |
<tr> | <tr> | ||
- | <td align=" | + | <td align="right">Tip: Clicking on the points indicates information about the value.</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td align="center">< | + | <td align="center"><iframe width="600" height="371" seamless frameborder="0" scrolling="no" src="https://docs.google.com/spreadsheets/d/1vw-DQQy8I5AZZXzox8GUeXIDSOYhLwpElEbce8H6Y90/pubchart?oid=134888037&format=interactive" align="middle"></iframe><br></td> |
</tr> | </tr> | ||
- | + | <tr> | |
+ | <td align="center"><font size="3" face="Verdana"><strong>Fig4.2 Model2</strong></font></td> | ||
+ | </tr> | ||
+ | |||
+ | </table> | ||
</div> | </div> | ||
<br> | <br> |
Latest revision as of 17:02, 17 October 2014
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