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imported>Myeongji Park
 
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<p><strong>Lecture 3 - Genomics</strong></p>
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<p><span style="font-size:14px"><strong>Lecture 3 - Genomics</strong></span></p>
  
 
<p>* What is <u>Genomics</u>?<br />
 
<p>* What is <u>Genomics</u>?<br />
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&nbsp;&nbsp; &nbsp; &nbsp; - After assmbling genome of one species, we can use it as reference genome.<br />
 
&nbsp;&nbsp; &nbsp; &nbsp; - After assmbling genome of one species, we can use it as reference genome.<br />
 
<br />
 
<br />
&nbsp;&nbsp;&nbsp;► MRCA : most recent common ancestor -&gt; we can predict&nbsp;</p>
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&nbsp;&nbsp;&nbsp;► MRCA : most recent common ancestor -&gt; we can predict similarity between different species.</p>
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<hr />
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<p>&nbsp;</p>
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<p>&nbsp;</p>
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<p>** Summary **</p>
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<p>(1) Genomics is changing the paradigm of biology.<br />
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(2) Geno-Pheno associated mutation is the key.<br />
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(3) Close species provide exact variants for pin-pointing mutation sites.<br />
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(4) Efficient reference to resequencing data comparison will be a useful bioinformatics methodology.<br />
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<br />
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<br />
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&nbsp;</p>
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<hr />
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<p><strong><span style="font-size:14px">Presentation 1. &quot;5<sup>th</sup> generation sequencing&quot;</span></strong></p>
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<p>► Design own model of sequencing.</p>
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<p>► Idea<br />
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&nbsp;&nbsp; &nbsp;(1) different H-bond of bases -&gt; nanosensor based on DNA helicase -&gt; sort AT, GC base pairing + measure change of current based on difference of size (pyrimidine vs. purine)<br />
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&nbsp;&nbsp; &nbsp;(2) detect decresing ATP, incresing ADP, and Pi.<br />
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&nbsp;&nbsp; &nbsp;(3) using dsDNA -&gt; break bond -&gt; sequencing</p>
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<p>&nbsp;</p>
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<p>[[ 1._Lecture ]]</p>

Latest revision as of 22:18, 31 May 2017

Lecture 3 - Genomics

* What is Genomics?
   ► We should remember two things.
       - 'T' = 7 billion persons (species diversity) + 7 billion bases (variability in one person)
          
   ► Every life or species have genome, and variation of each genome is different.

 

* GEP/T graph.
   ► Geno + Enviro -> Pheno/Trait (almost cases are disease)
      
      - Prediction is conducted by experiment, bioinformatics, etc.

   ► The challenge : As life is so complicated, prediction is so hard. We have to consider environmetal complexity with genomic complexity.
      - Possible solution : using AI based on big data.

   ► Solutions
       (1) Exact large amount of data.
           - It is so important.
           - typing (cheap and efficient) : simple test, approximation (not 100% prediction).
           - sequencing (ultimate) : almost 100% prediction, digital device, it can have error (we don't know reason of error), ex) hardware.
       (2) Need principle, law, and algorithms.
           - We need to know related principle when we face to some facts.
       (3) Big computer.
   

* Genome sequencing.
   ► 2nd generation : multiple molecule -> approximation
   ► 3rd generation : single molecule
   ► 4th generation : nanopore + membrane

   ► Base calling : computer notifies types of bases.
   ► NSG Data analysis : mapping based on reference gene.


* Close species comparative genomics.
   ► If we sequencing genome of new species, we have to find and get right right samples.
       - we should pick sample which has interesting phenotype.
       - And then, set up experimental design.

   ► Gene assembly : assemble gene fragments after putting the known gene between the intereted gene fragments.
       - expensive
       - After assmbling genome of one species, we can use it as reference genome.

   ► MRCA : most recent common ancestor -> we can predict similarity between different species.


 

 

** Summary **

(1) Genomics is changing the paradigm of biology.
(2) Geno-Pheno associated mutation is the key.
(3) Close species provide exact variants for pin-pointing mutation sites.
(4) Efficient reference to resequencing data comparison will be a useful bioinformatics methodology.


 


Presentation 1. "5th generation sequencing"

► Design own model of sequencing.

► Idea
    (1) different H-bond of bases -> nanosensor based on DNA helicase -> sort AT, GC base pairing + measure change of current based on difference of size (pyrimidine vs. purine)
    (2) detect decresing ATP, incresing ADP, and Pi.
    (3) using dsDNA -> break bond -> sequencing

 

1._Lecture