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To use DNA to identify a specific person accurately, you want to compare genetic markers that are unlikely to be shared with any other person.

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When comparing the DNA fingerprints of a parent and child the parent's DNA fingerprint must have?

DNA bands that match those in the child's fingerprint and that aren't from the other parent.


What is the term for genetic markers that turn DNA segments on and off?

The term for genetic markers that turn DNA segments on and off is "epigenetic markers." These markers do not alter the DNA sequence but control gene expression by regulating access to specific regions of DNA.


How many markers are used to make a dna profile?

In forensic DNA analysis, a DNA profile is typically created using 20 genetic markers. These markers are specific regions of the genome that vary between individuals and are used to establish a unique genetic fingerprint for identification purposes.


What conclusion cannot be made from two DNA fingerprints that show identical patterns?

If two DNA fingerprints show identical patterns, we cannot conclude that the individuals from whom the samples were taken are the same person. This is because identical DNA patterns can occur in identical twins, or the samples may come from different individuals with coincidentally similar genetic markers. Additionally, identical patterns do not indicate the specific relationship between the individuals, such as whether they are related or unrelated.


How many markers are in a DNA profile?

A DNA profile typically consists of 13 to 20 specific markers, known as short tandem repeats (STRs), which are analyzed for forensic and identification purposes. These markers are chosen for their variability among individuals, making them useful for distinguishing between different DNA profiles. The exact number of markers can vary depending on the protocols used by different labs or for specific applications.

Related Questions

When comparing the DNA fingerprints of a parent and child the parent's DNA fingerprint must have?

DNA bands that match those in the child's fingerprint and that aren't from the other parent.


What is a genetic makers?

Genetic markers are specific sequences of DNA that can be associated with particular traits or diseases. They serve as biological signposts, helping researchers identify genetic variations linked to certain conditions or characteristics. These markers can be used in various applications, including genetic mapping, disease diagnosis, and personalized medicine. By analyzing genetic markers, scientists can gain insights into inheritance patterns and genetic predispositions.


What if you sent human saliva to the dog breed DNA test?

The results would be voided because the genetic markers for the "breed" genetic or parental markers would not be present.


What is the term for genetic markers that turn DNA segments on and off?

The term for genetic markers that turn DNA segments on and off is "epigenetic markers." These markers do not alter the DNA sequence but control gene expression by regulating access to specific regions of DNA.


Why do humans have unique DNA fingerprints?

All humans are made up of the same DNA. Thymine always pairs with adenine and guanine always pairs with cytosine. However the reason we all have different finger prints is because there are numerous combinations that a sequence could be. I could be ATTACG while you could be CAGTTAT. They are made of the same genetic material but they are different because of their sequence. DNA can also be different lengths, so unless there is a clone it is impossible for a sequence to reoccur in humans. Some areas of the sequence may be the same but never the whole thing. Hope this helps! :)


How can one create a linkage map for genetic analysis?

To create a linkage map for genetic analysis, one must first identify genetic markers that are inherited along with the gene of interest. These markers are then used to track the inheritance patterns of the gene through generations. By analyzing the frequency of recombination events between the gene and the markers, the relative positions of the gene and markers on a chromosome can be determined, creating a linkage map.


What are genetics markers?

Genetic markers are areas on the chromosome which are in linkage disequilibrium with a known trait, ie they are inherited along with the trait. The markers do not have to cause the condition or trait to be observed, but they will always be inherited alongside the trait and therefore cna be described as a marker for that particular trait.


What is codominant and dominant markers?

Dominant markers are high efficiency markers that allow the analysis of many loci per experiment without requiring previous information about their sequence. Co-dominant markers are allows the analysis of only a single locus per experiment, so they are more informative because the allelic variation for that locus can be distinguished.


How many markers are used to make a dna profile?

In forensic DNA analysis, a DNA profile is typically created using 20 genetic markers. These markers are specific regions of the genome that vary between individuals and are used to establish a unique genetic fingerprint for identification purposes.


What is the Difference between physical marker and genetic marker?

Physical markers are easily observable traits like eye color, while genetic markers are specific sequences in the DNA that are associated with a particular trait or disease. Physical markers can be seen directly, while genetic markers require testing to identify.


How are genetic markers related to transformation?

Genetic markers make it possible for researchers to mix recombinant plasmids with a group of bacteria. Add enough DNA to transform one cell into a million and still be able to "find" that cell.


How to interpret sibling DNA test results and understand the genetic relationship between siblings?

Interpreting sibling DNA test results involves comparing the genetic markers shared between siblings to determine their genetic relationship. The more markers they share, the closer their genetic relationship. Understanding the genetic relationship between siblings can help identify common ancestry and potential health risks.