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What has been the human goal of the human genome projects?
to identify every human gene
What is the human genome project an attempt to do?
The Human Genome Project was the effort to identify the 20,000-25,000 genes in human DNA. Once they had been identified they sequenced the 3 billion chemical base pairs that are present in human DNA, and stored this information in databases. This was a 13-year project that was completed in 2003. The Human Genome Project allowed scientists to better pinpoint genetic diseases and will help to find cures for these disorders.
Does every prime number appear in the Euclid-Mullin sequence?
This is an unsolved problem in mathematics. However, as of 2012, the prime 41 had not been known to appear in the Euclid-Mullin sequence.
Did Harry Potter turn into a human at the end?
Harry Potter has always been a human, he just had powers that not every human had.
Do angels protect humans?
Many christian denominations believe that every human (or at least every christian human) has been assigned a guardian angel to protect them.
Why the bones in the human ear have been given their names?
Every bone has a name
Where were traces human life found?
Traces of human life has been found on every corner of the globe. Including in the poles.
Did Cherokee have pets?
Yes Pets have been part of every human culture from the beginning of human existence.
Have thai girl ever cheat thai guy's heart?
There has been cheating in every culture at every time in human history.
What goal of the human genome has been achieved?
To map & sequence all of the DNA base pairs of the human chromosomes.
What bacterium undergoes mutation caused by an antibiotic. Specifically the gene with the sequence AUGCCCACCCGA undergoes a frameshift mutation. Which of these sequences represents the mutated gene?
A frameshift mutation occurs when nucleotides are inserted or deleted from a DNA sequence, shifting the reading frame of the gene. Given the original sequence AUGCCCACCCGA, a potential mutated sequence could be AUGCCCA---CCGA, where a nucleotide has been deleted, resulting in a shift. Without specific options to choose from, it's essential to identify a sequence that deviates from the original by an insertion or deletion that disrupts the reading frame.
How do you identify component defects that have been removed?
how to identify component defects
