Team:CBNU-Korea/Project/GD/Overview

From 2012.igem.org

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different genus (For example, like Mycoplasma, Salmonella, that
different genus (For example, like Mycoplasma, Salmonella, that
the essential gene is already identified experimentally), and
the essential gene is already identified experimentally), and
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secure the reliability of our analysis method. Secondly, we infer
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secure the reliability of our analysis method. Secondly, we
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the accurate sequence of the essential genes that we analyzed.<br>
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presume specific genes which reflect the characteristic of genome.
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~~<br> We believe that if this analysis becomes perfect, our
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We think that there are genes that the function of it can
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analysis method will secure reliability and give you the accurate
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represent each genome or each level. In this year we only analyzed
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outcome. Also hoping that you will use our program more actively,
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every genome in Streptococcus, so we cannot provide information of
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we are planning to provide information you will need(For example,
+
specific genes. But we expect that the specific genes that we
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restriction enzyme sites, Gene map, the culture conditions of
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analyzed in this year not only make our software more wealthy but
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different species). We hope our program (Program name) will
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also make accurate result. Thirdly, we presume accurate
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provide the fundamental information for your experiment in the
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arrangement of essential gene that we analyzed. Because we mostly
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near future.
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concentrated on the analysis of strand pattern, it isn’t enough to
 +
provide accurate arrangement. However we know that we need the
 +
information of the order of genes to make complete design
 +
software. Thus we are going to analyze this and improve the
 +
completeness of our Designer.<br> We believe that if this
 +
analysis becomes perfect, our analysis method will secure
 +
reliability and give you the accurate outcome. Also hoping that
 +
you will use our program more actively, we are planning to provide
 +
information you will need(For example, restriction enzyme sites,
 +
Gene map, the culture conditions of different species). We hope
 +
our program Minimal Genome Designer will provide the fundamental
 +
information for your experiment in the near future.
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</p>
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Revision as of 18:59, 26 September 2012

Minimal Genome Designer

- Overview

1. Overview

1-1. Predicting Essential Genes

1) Need of the Analysis of Essential Genes

It is thought that today, Synthetic Biology has reached a plateau. Since the success of the experiment that re-synthesizes the genome and insert it into the cell, it seems that Synthetic Biology is not developing. But if somebody can design a genome and synthesize it, synthetic biology can take off again. Then what do we need to design a genome? First, we need information about essential genes. An essential gene is a gene that is critical for survival. If you have the information about the essential gene, you are in a superior state in making human artificial cell in a true sense. Because it means that you already have the ability to make the brick. All you have to do is make a brick with our program developed for you according to the sequence of the essential genes, and conduct experiments.

2) The Present of the Analysis of Essential Genes

Essential genes are being analyzed in many places, such as in DEG or PATRIC.

3) The Problem of the Analysis of Essential Genes

Essential genes known today are mostly discovered with in vitro experiments. As seen in the chart above, the result of the experiment can vary according to conditions and methods. We bring forth a problem about this. We believe that to give meaning to a result, it has to be accurate. Also the analysis method of essential genes used today takes a lot of time and labor. To address this we use a bio-informatics way and find essential genes.

1-2. Analysis of Essential Genes

1) Definition of Essential Genes

As we are using the computer to find essential genes, we can't use the existing method to analogize essential genes with experiments. We assume that if essential genes are critical to living, every organism must have it. So we approached the problem with the assumption that an essential gene is a gene that every living thing will has.

2) Significance of the Analysis of Essential Genes

We are proud of our analysis methods. You will see that our analysis result is not that different from that proved with experiments. Our analysis results do more than finding essential genes. With this, you can understand the metabolic process and furthermore have a good chance to synthesize an artificial cell.

1-3. Developing of the Minimal Genome Designer

1) The Purpose of Minimal Genome Designer

The purpose of our program is fundamentally to understand the structure and the principle of the genome. However, we will not stop at understanding the information about genome, but hope that you can go on to build your own genome by using the brick in your experiment.

2) Advantages of Minimal Genome Designer

Minimal Genome Designer will make you easily understand the genome, by showing you the structure. Providing various information about the gene and the genome, our program will shorten your time to design the experiment. This also means that you can save money as well. We have tried and verified so that Minimal Genome Designer can procure reliability. The results made by Minimal Genome Designer can be used as a new background information for your experiment.

2. Function

2-1. Viewer

1) The program is installed and run in a local computer. The local database isn't included in the program, and to see the database you should have access to the server that we constructed.

2) The program consists of the circular viewer on the upper left, and the linear viewer below, and a Genome list on the right.

3) First, select a gene in the Genome List on the right. You may select it on the Tree View, or by searching the gene that you want. After selection, the information of the gene will be shown in graphic. You can see more information about the relevant gene and the genome on the Genome Information in the middle.

4) If you move the reading glass image of the circular viewer, you can see the relevant location in linear graphic. By using the linear scroll bar, you can change the linear location. If you click the relevant square image in the linear viewer, you can see more information about the gene(Like sequences, length, location, Synb_id, function, product and more).

5) With the check box on the lower right-hand corner of the circular viewer, you can check the gene of your choice.

6) By checking the By COG check box, you can see each of the COG functions of each gene. Choose the COG function in the scroll box that appears after you check, then you can see the genes including that function.

7) If you check the DEG Only check box, you can see the informations that DEG has found in vitro in visual.

8) If you check the EG Only check box, you can see the information on essential genes that we gain through analysis in visual.

9) Select 'History' in the Genome List menu, then you can see all the genes that have seen all along easily.

2-2. Unique Genome Designer

1) Shows the information of essential genes that can exist in each section.(Function, Product, COG number etc.)

2) Shows the frequency of the essential genes in each section that are analyzed using 82 different species.

3) Shows the frequency of the COG of each section that is analyzed using 82 different species.

4) By choosing each section of 20 in the screen, the essential genes that can be inserted in the relevant area will be listed.

5) The user can put the wanted essential gene In each section and see the processing situation. When the whole 478 essential genes are put in all sections, the design is completed.

7) The user can save and import the designing situation as a XML form at their convenience.

8) When the user complete the design, the designed minimal genome can be saved as a XML form and it could be viewed at Viewer.

3. Future Work

Our ultimate objective is to make a program that can build a complete minimum genome. Well do we know the information that we need to realize our goal. First, we analogize essential genes that every species is supposed to have. And we are aware of the fact that to achieve this goal, our analysis method needs higher reliability. Therefore, we are going to use the same method on a different genus (For example, like Mycoplasma, Salmonella, that the essential gene is already identified experimentally), and secure the reliability of our analysis method. Secondly, we presume specific genes which reflect the characteristic of genome. We think that there are genes that the function of it can represent each genome or each level. In this year we only analyzed every genome in Streptococcus, so we cannot provide information of specific genes. But we expect that the specific genes that we analyzed in this year not only make our software more wealthy but also make accurate result. Thirdly, we presume accurate arrangement of essential gene that we analyzed. Because we mostly concentrated on the analysis of strand pattern, it isn’t enough to provide accurate arrangement. However we know that we need the information of the order of genes to make complete design software. Thus we are going to analyze this and improve the completeness of our Designer.
We believe that if this analysis becomes perfect, our analysis method will secure reliability and give you the accurate outcome. Also hoping that you will use our program more actively, we are planning to provide information you will need(For example, restriction enzyme sites, Gene map, the culture conditions of different species). We hope our program Minimal Genome Designer will provide the fundamental information for your experiment in the near future.