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DNA sequencing using the Maxam Gilbert method is now the less common of the two most known DNA sequencing methods. It is accurate, but very slow. It was first discovered some time in the mid 1900s.

The Maxam Gilbert method relies on cutting billions of different DNA strands at various cites to produce different strands of discrete (each different) lengths. Imagine this: 5 - AATCGGTAGGCTACGTAGTCGACTGCATCGACTACG - 3.

Now there are many As, Ts, Gs, Cs in this strand. However, the goal is to cut the strand starting at the 5' end into successive nucleotide sequences.

You keep on doing this until you get these sequences:

A

AA

AAT

AATC

AATCG - now remember so many cuts are going on (billions) that it actually works this out perfectly.

These different DNA strands are then run through a DNA electrophoresis gel. There are millions of strands of equal lengths; millions of As AAs AATs and so on. These millions all migrate to the same place in the gel to create a very distinct band.

Certain nucleotides (let's say on the G of AATCG) actually contain radioactive tags. This is how you tell the different nucleotides apart. This produces distinct bands on an x-ray film where the bands of DNA are (because the DNA contains a radioactive substance).

You'll end up with a gel that looks like this: Take a ruler, go to each line and read what letter it is. Doing it this way, you'll get the genome (normally to around 500-800 base pairs). It takes a while, and that's why we all love the way computers do it all for us today.

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