The ability to equalize the DNA binding stability of comprehensive set
s of oligonucleotides is imperative for the application of sequencing
by hybridization technology. By substitution of ribonucleotides into a
n oligonucleotide composed of deoxyribonucleotides, and vice versa, th
e duplex stability of the oligonucleotide is changed linearly with the
number of serial alternations of sugar configurations within the mole
cule. Since this effect occurs independently of the actual base sequen
ce, any set of oligonucleotides could be adjusted to a defined level o
f binding stability.