DNA sequencing is the process of determining the order of nucleotides in a DNA fragment. The first DNA sequencing method, called Sanger sequencing, was developed in 1975 and involves copying DNA fragments and labeling the fragments to determine the sequence. DNA sequencing is useful for scientists as it allows study of what DNA codes for through comparative and functional genomics. While it improves healthcare and agriculture, a disadvantage is the risk of providing an incorrect DNA sequence.
2. What is DNA Sequencing?
DNA Sequencing is finding the order of nucleotides in a fragment of DNA
These 4 bases are cytosine, guanine, adenine, or thymine.
3. History of DNA Sequencing
This method was founded in 1975 by Frederick Sanger
This method was named after him and called Sanger Sequencing
4. How the Sanger Method Works
Is similar to the process of DNA replication
Sanger method uses non-real radioactively-labeled bases that help stop
DNA replication
These fake nucleotides are colored corresponding to the nucleotides so
that scientists know how to read them
5. The First Step
First, many copies of the DNA fragment are needed to be made.
To do this, scientist use the Polymerase Chain Reaction that heats and
cools DNA to make quick copies of the fragment
6. The Next Step
Fragments are heated again to be unwound in to single-stranded DNA
Then a primer is added which binds to the DNA
ddNTPs are added
7. The Final Step
The DNA strand is run through Gel Electrophoresis which sorts the
fragments by size
8. How DNA Sequencing is helpful to
Scientists
Used in field of functional genomics which is the study of what certain
DNA fragments codes for and what DNA fragments code proteins
Also used in field of comparative genomics which compares organisms DNA to
other organisms to find out more about the organisms history.
9. The Advantages of DNA Sequencing
Improve health care
Helping plants and animals to be able to resist certain diseases
Helps in forensic science for identifying criminals
10. The Disadvantage
The risk that the DNA sequencing may not work right and provide the
wrong DNA sequence of that fragment