Patient genetic profilesYour nameInstructorCourseDatePatient genetic profilesPatient genetic profile is the study of specific genes and the variations and expression ofthose genes on a particular tissue or an individual. It is used to diagnose a disease and understandthe treatment to undergo by the use of drugs or radiations ("2020 Topics and Objectives ObjectivesAZ | Healthy People 2020", 2018).This is a study of understanding the genetic formation from theparents to the offspring. In this paper I will differentiate current tools used tools available topublic to conduct and manage family genome profile, importance of family genomic completion,ethical and political implications surrounding family genomic profiles and tools used in myworkplace.There are many tools which are used to determine the family genomic profiles. Theyinclude newborn screening, the diagnostic testing, the carrier testing, the prenatal testing, the preimplantation testing, the predictive and presympptomatic testing, and the forensic testing(Reference, 2018).In newborn screening a test is carried out after birth so as the baby can betested for disorders. The main disorders that are tested are phenylketonuria and congenitalhypothyroidism. In diagonistic testing one is tested for chrosomal formation. This test can bedone before birth or even during persons life so as to test for any disorder. Carrier testing isdone so as to identify whether a person has carried one cop ...

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