Detection system for PCR assay

1. A homogeneous assay detection system for a PCR process using FRET which comprises at least one unlabelled tailed primer, a first single-labelled Oligonucleotide sequence, the first single-labelled Oligonucleotide sequence being a primer from which DNA synthesis may be initiated, the unlabelled tailed primer having a tail region comprising an Oligonucleotide sequence identical to a portion of the first single-labelled Oligonucleotide sequence, and at least a second single-labelled Oligonucleotide sequence, the first and second Oligonucleotide sequences being of differing Tm, in which the first and second Oligonucleotide sequences hybridize to one another in free solution to form a fluorescent quenched pair, that upon introduction of a complementary sequence to one or both sequences at least one of the single-labelled Oligonucleotides hybridizes to a complementary sequence and initiates DNA synthesis, the said at least one single-labelled Oligonucleotide no longer being able to hybridize to the other single-labelled Oligonucleotide, whereby one or both sequences generates a measurable signal, one of the sequences being of a Tm that is below the Ta of the PCR process.

2. A detection system as claimed in claim 1 , incorporated in a PCR system to detect a specific sequence, wherein said first single-labelled Oligonucleotide sequence and second single-labelled Oligonucleotide sequence differ by more than 10 bases in length.

3. A detection system as claimed in claim 1 , wherein the introduction of a complementary sequence is by the production of DNA sequences via PCR.

4. A detection system as claimed in claim 1 , wherein the PCR process is monitored in real time at each cycle or after a number of cycles whereat the reaction has otherwise not yet generated enough product to create a measurable signal by lowering the temperature of the reaction to allow hybridization to occur.

5. A detection system as claimed in claim 1 , wherein said first sequence has a Tm that is above the Ta of the PCR process.

6. A detection system as claimed in claim 1 , wherein said second sequence has the quencher label of the fluorescent quenched pair.

7. A detection system as claimed in claim 1 , wherein the PCR process is allele specific PCR based SNP Genotyping.

8. A detection system as claimed in claim 2 , wherein the PCR process is monitored via the use hybridization only.

9. A detection system as claimed in claim 8 , wherein the PCR process is monitored via the use hybridization only post PCR.

10. A detection system as claimed in claim 1 , wherein the fluorescent quench oligo pairs range from 6 bp to 100 bp.

11. A detection system as claimed in claim 10 , wherein the fluorescent quench oligo pairs range from 6 bp to 100 bp but are not matched in length.

12. A detection system as claimed in claim 1 , wherein the fluorescent quench oligo pairs are labelled both with fluorophores.

13. A detection system as claimed in claim 1 , wherein the fluorescent quench oligo pairs are labelled one of the pair with a fluorophore and the other with a non fluorescent quenching molecule.

14. A detection system as claimed in claim 1 , wherein the fluorescent quench oligo pairs are modified to be resistant to nuclease degradation.

15. A detection system as claimed in any preceding claim, wherein the fluorescent quench oligo pairs are labelled with molecules that are distant sensitive.

16. A detection system as claimed in claim 15 , wherein the PCR process is monitored via the use of hybridization only.

17. A detection system as claimed in claim 1 , wherein the fluorescent quench oligo pairs contain modified nucleotide bases.

18. The detection system as claimed in claim 1 , in which the first single-labelled Oligonucleotide primer sequence has an unmodified 3′ base from which DNA synthesis is initiated.

19. A detection system as claimed in claim 1 , further comprising at least one unlabelled tailed primer, the tail comprising a DNA sequence identical to a portion of the first single-labelled Oligo sequence.