How can DNA Sequencing be used to identify other classes of Pathogens?

How can DNA Sequencing be used to identify other classes of Pathogens?

What is DNA Sequencing?

DNA sequence means to determine the order of four chemical components of the DNA molecule-known as “bases.” The sequence shows the genetic information in a specific segment of DNA to researchers. In order for researchers, for example, to identify which sections of DNA contain genes, which extend carry regulatory instructions or turn genes on or off, sequential data can be used. Moreover, sequence data can highlight modifications to a gene that can cause disease.

The four chemical bases are always tied together in the DNA double helix and are made into “base pairs.” Adenine(A) always matches thymine (T); cytosine(C) always matches guanine (G). This pairing serves to copy DNA molecules when the cells are separated, and pairing is the basis for the methods used to perform most experiments in a DNA sequence. The human genome contains about 3 billion base pairs that describe how to make and preserve a person.

How can DNA Sequencing be used to identify other classes of Pathogens?

How does DNA Sequencing Identification work?

Once the DNA is sequenced the data can be directly compared to understand the similarity thats what the sequence is for.

They compared data then gives out the closest family they below and it becomes easier to identify the organism be it Bacteria or other.

Researchers are now in a position to easily and cheaply compare vast parts of DNA from various people-1 million or more bases. Such comparisons may provide tremendous information on the role of the heritage in disease susceptibility and environmental effects. Moreover, the ability to more quickly and efficiently sequence the genome provides tremendous potential for diagnostics and treatments.

Although the standard DNA sequencing is still long in the doctor’s office, a sequence has been used in a number of major medical centres to diagnose and treat such diseases.

You are simply able to submit them into the databases in the process that will then identify them for you just like the normal search query.

How can disease sequencing be used to identify genetic risk for certain diseases and disorders?

By being able to sequence DNA, you are able to see genetic disorders that could not only affect the future of the patient but also the risk for future offspring. A disease that is heritable could be seen and save future lineages from suffering. You could also use it to find out species that the DNA came from to identify and organize.

Explain why antibodies allow scientists to target and identify specific disease agents.

Since antibodies are used to attack specific invaders, by knowing the antibody you are able to figure out the antigen it attacks. This could then lead to knowing what disease these antigens come from since you know the antibodies it triggers.

How can scientists identify specific bacteria when they are amplifying and studying the same region of DNA in each species?

They are able to use new technology which has mapped out all the parts of DNA. They are then able to locate the specific bacteria by just using a computer by searching for the bacteria’s own tags and sequences.

How can DNA Sequencing be used to identify other classes of Pathogens?

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