High Throughput Sequencing

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===== Step 1  =====
 
===== Step 1  =====
  
Double stranded DNA (dsDNA) is randomly fragmented to blund ended pieces. Attach adapters to either end of the fragmented [[DsDNA|dsDNA]]&nbsp;via blunt end ligation. Two adapters are added separately so both ends of the [[DNA|dsDNA]] have an adapter present.<br>  
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Double stranded DNA (dsDNA) is randomly fragmented to blund ended pieces. Attach adapters to either end of the fragmented [[DsDNA|dsDNA]]&nbsp;via blunt end ligation. Two adapters are added separately so both ends of the [[DNA|dsDNA]] have an adapter present. These adapters are complementary to the oligonucleotides present on the flow cell.<br>
  
 
===== Step 2<br>  =====
 
===== Step 2<br>  =====

Revision as of 11:32, 12 October 2014

High Throughput Sequencing (also known as Illumina Solexa DNA sequencing) is a technique used to sequence DNA or cDNA via fragmenting the genetic information randomly. RNA can also be sequenced but involves additional steps to those shown below. Firstly mRNA is hydrolysed by magnesium catalysed reaction to give fragments and then the sequences are randomly primed by reverse transcription [1].

The Process:

Contents

Step 1

Double stranded DNA (dsDNA) is randomly fragmented to blund ended pieces. Attach adapters to either end of the fragmented dsDNA via blunt end ligation. Two adapters are added separately so both ends of the dsDNA have an adapter present. These adapters are complementary to the oligonucleotides present on the flow cell.

Step 2

Denature the dsDNA to ssDNA and wash over flow cell channels. The adapters will enable binding to the dense lawn of primers on the flow cell.

Step 3

Bridge Amplification- The free end of the fragment bends and hybridises to a separate complimentary primer on the flow cell forming a 'bridge'. Unlabelled nucleotides and enzymes are then added to the flow cell to initiate amplification of the second strand of DNA.

Step 4

Denature DNA back into single stranded fragments and the process is repeated to produce clusters of identical DNA around the original sequence.

Step 5

First Chemistry Cycle- Add four reversible terminators, primers and DNA polymerase to the flow cell. Each cluster will show up as spot after laser excitation due to the added bases fluorescence. The blocked 3' OH terminus and the flurophone from each base are then removed to allow another base to be added to the sequence. This will eventually allow the full sequence to be built up.

References

  1. Mardis ER. (2008), "Next-generation DNA sequencing methods", Annu Rev Genomics Hum Genet.,9:387-402

Mardis ER (2008) Next-generation DNA sequencing methods.Annu Rev Genomics Hum Genet. 9:387-402

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