DNA Testing in Humans - Project
DNA Testing in Humans - Project
Polymerase Chain Reaction (PCR): Amplifies small DNA samples for further analysis.
DNA Sequencing: Determines the exact sequence of DNA bases, revealing genetic
variations.
Gel Electrophoresis: Separates DNA fragments based on size for comparison.
Microarray Analysis: Identifies genetic markers related to health conditions and
ancestry.
Medical Insights: Helps detect genetic predispositions to diseases like cancer and
Alzheimer's.
Ancestry & Heritage: Provides information about ethnic backgrounds and ancestral
origins.
Forensic Applications: Assists in criminal investigations and identification of remains.
Personalized Medicine: Enables tailored treatments based on genetic profiles.
Family Planning: Identifies hereditary conditions that may be passed to offspring.
DNA testing has revolutionized healthcare, forensics, and genealogy but poses ethical
and financial challenges.
Ongoing advancements in biotechnology will continue to enhance accuracy and
accessibility.
References:
o National Human Genome Research Institute (NHGRI)
o Centers for Disease Control and Prevention (CDC)
o Scientific journals on genetic testing