Scientists study mutations to learn about genetic differences in a few ways:
DNA Sequencing: This is a method that allows scientists to read the DNA code. It helps them find mutations, which are changes in the DNA.
Molecular Markers: These are tools that help researchers track specific gene changes linked to traits. They estimate that about 1 in every 1,000 DNA building blocks varies from person to person.
Population Studies: Scientists look at genetic samples from different groups of people. They found that roughly 85% of genetic differences don’t affect how we live. About 10% can be harmful, while 5% can actually be helpful.
These methods help scientists understand the different mutations in our genes.
Scientists study mutations to learn about genetic differences in a few ways:
DNA Sequencing: This is a method that allows scientists to read the DNA code. It helps them find mutations, which are changes in the DNA.
Molecular Markers: These are tools that help researchers track specific gene changes linked to traits. They estimate that about 1 in every 1,000 DNA building blocks varies from person to person.
Population Studies: Scientists look at genetic samples from different groups of people. They found that roughly 85% of genetic differences don’t affect how we live. About 10% can be harmful, while 5% can actually be helpful.
These methods help scientists understand the different mutations in our genes.