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Therefore, the resolution of the system is at a few nucleotides.
Only a few percent of the nucleotides differ from one species to the next.
It will mark off every last nucleotide, but there are billions of them.
Usually they occur in regions where the nucleotides seem to be doing nothing.
These blocks are called nucleotides and come in four varieties.
This process is used to determine the order of nucleotide bases.
A difference of two or more nucleotides is generally considered to be an exclusion.
The longest sequence also increased from 780 to 2,353 nucleotides.
To do this, the first nucleotide in the sequence must be detected.
Their minimum size is 246, but they can produce forms from 287 to 301 nucleotides.
Among our 3 billion nucleotides, an estimated 10 million are locations of common variations.
These occur at specific individual nucleotide positions within a gene.
The stars indicate nucleotides that are identical in all three species.
"A test of neutral molecular evolution based on nucleotide data".
A nucleotide substitution is a base change between two populations.
The simplest case of an overhang is a single nucleotide.
Its length is 15,179 nucleotides and it contains 13 genes.
A series of three nucleotide bases that form Genetic code.
I don't want to get too heavily into the details of the individual nucleotides.
A similar illustration is provided using a sample nucleotide sequence.
However, at the nucleotide level they are only 86% identical.
The genome has been sequenced and is only 73 nucleotides long.
Each of these smaller molecules is called a nucleotide.
Thus it is possible to change up to about a third of the nucleotides in an open reading frame and still produce the same protein.
In this case, information about single nucleotide variants will be of limited utility.