This process is used to determine the order of nucleotide bases.

For example, among humans, about 1 in every 1,200 nucleotide bases differ.

Underlying this utility are the bioprogrammable interactions between complementary nucleotide bases.

The genome consists of a single open reading frame that is 9600 nucleotide bases long.

The idea was to see if binary digit pairs might match nucleotide bases.

To this backbone are attached the four nucleotide bases.

Hundreds of groups worked together to produce the sequencing of the three billion nucleotide bases in the human genome.

Mutations can result in the addition or deletion of one or more nucleotide bases.

This is a genetic mutation at the level of nucleotide bases.

Release 194, produced in February 2013, contained over 150 billion nucleotide bases in more than 162 million sequences.