Respuesta :
Knowing which genes—when they are dysfunctional—cause which diseases will make it easier to diagnose patients and give information on the functional traits of the mutation.
With the development of modern high-throughput sequencing methods and the knowledge gained from the expanding area of genomics, illness genes are being identified more quickly, enabling researchers to find more complex mutations. Techniques for identifying disease genes frequently use the same general process. First, DNA is taken from a number of patients who are thought to share a hereditary condition. Their DNA samples are then examined and screened to identify likely areas where the mutation may exist. The following list includes these methods. The mutant gene should be located in the region that overlaps when these likely locations are lined up next to one another. Candidate genes are looked for in a region of the genome where sufficient sequence information is available. These genes' coding areas are then sequenced up until a mutation is found or another patient is identified, at which point the research can be repeated, potentially focusing on a smaller region of interest.
To learn more about map disease genes, refer: https://brainly.com/question/13776652
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