They use DNA sequencing to identify species via genetic differences.
The four chemical "bases" that make up the DNA molecule must be identified in the correct order in order to sequence DNA. The sequence provides information to scientists about the type of genetic data that is contained in a certain DNA segment.
For instance, scientists can utilize sequence data to identify the DNA segments that contain genes and the segments that carry regulatory instructions that switch genes on and off. Furthermore, and this is crucial, sequencing data might point out variations in a gene that might be harmful.
Large DNA lengths, 1 million bases or more, from various individuals can now be compared swiftly and affordably by researchers. Such comparisons can reveal a wealth of information regarding how inheritance affects illness susceptibility and how the body reacts to environmental factors. The potential for diagnostics and treatments is also greatly increased by the faster and more affordable genome sequencing.
The biology of development and evolution can also be better understood by comparing the genomic sequences of other animals and species, like yeast and chimpanzees.
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