Quantitative multiplexed identification of nucleic acid targets

1. A method for detecting in a sample at least one of a plurality of target nucleic acid molecules, the method comprising the steps of:

identifying a first amplification region of each of said plurality of target nucleic acid molecules, wherein the first amplification region is conserved among said plurality of target nucleic acid molecules;

identifying a second amplification region of each of said plurality of target nucleic acid molecules, wherein the second amplification region is not conserved among said plurality of target nucleic acid molecules, and further wherein for each one of the plurality of target nucleic acid molecules, the first amplification region and the second amplification region are in different locations of the nucleic acid molecule;

generating an amplification reaction mixture, the mixture comprising at least two different target nucleic acid molecules, a first primer pair designed to amplify said first amplification region, a second primer pair designed to amplify said second amplification region, and a first nucleic acid probe designed to hybridize to said first amplification region;

producing, simultaneously in an amplification reaction comprising the reaction mixture, a first amplification product of the first amplification region of each target nucleic acid molecule present in said sample and a second amplification product of the second amplification region of each target nucleic acid molecule present in said sample, wherein the first and second amplification products are separate products;

detecting the production of said first amplification product in real time, wherein said first nucleic acid probe hybridizes to said first amplification region; and

detecting said second amplification product to indicate the presence of each target nucleic acid molecule present in said sample.

2. The method of claim 1 , wherein the step of detecting said first amplification product further comprises the step of quantifying the amount of target nucleic acid molecules present in said sample.

3. The method of claim 1 , wherein the step of detecting said second amplification product comprises hybridizing said second amplification product to a complementary probe.

4. The method of claim 3 , wherein said complementary probe is fixed to a substrate.

5. The method of claim 4 , wherein said substrate is a microarray.

6. The method of claim 1 , further comprising the steps of:

identifying a third amplification region of a second plurality of target nucleic acid molecules, wherein the third amplification region is conserved among said second plurality of target nucleic acid molecules;

producing a third amplification product of the third amplification region of each of said second plurality of target nucleic acid molecules present in said sample; and

detecting the production of said third amplification product in real time.

7. The method of claim 6 , wherein said first amplification product and said third amplification product are produced in the same reaction.

8. The method of claim 2 , further comprising the step of:

performing quantitative multiplexed detection of each of said plurality of target nucleic acid molecules present in said sample by analyzing both the quantified amount of target nucleic acid molecules present in said sample and the detected presence of each target nucleic acid molecule present in said sample.

9. The method of claim 1 , wherein the presence of one or more target nucleic acid molecules present in said sample indicates the presence of a pathogen in said sample.

10. The method of claim 1 , wherein the method is capable of detecting at least two pathogens in said sample.

11. The method of claim 1 , wherein the presence of one or more target nucleic acid molecules present in said sample indicates the presence of a specific nucleic acid sequence in said sample.

12. The method of claim 1 , further comprising the step of purifying nucleic acid from said sample.

13. The method of claim 1 , wherein the step of identifying a first amplification region of each of said plurality of target nucleic acid molecules comprises the steps of:

performing a sequence alignment of at least a segment of the nucleic acid sequence of each of said plurality of target nucleic acid molecules;

identifying said first amplification region based on said sequence alignment;

designing the first primer pair, the second primer pair configured to configured to amplify said first amplification region during the amplification; and

designing a probe that will hybridize to said first amplification region during the amplification of said region.

14. The method of claim 13 , wherein said probe is designed to have a melting temperature that is at least 6° C. higher than the melting temperature of said first primer and the melting temperature of said second primer.

15. The method of claim 1 , wherein the step of identifying said second amplification region of each of said plurality of target nucleic acid molecules comprises the steps of:

performing a sequence alignment of at least a segment of the nucleic acid sequence of each of said plurality of target nucleic acid molecules;

identifying said second amplification region based on said sequence alignment; and

designing the second primer pair, the second primer pair configured to amplify said second amplification region during the amplification.

16. The method of claim 15 , further comprising the step of designing a complementary probe that will hybridize to the second amplification region of each of said plurality of target nucleic acid molecules.

17. The method of claim 1 , wherein said first amplification product and said second amplification product are produced simultaneously.

18. The method of claim 1 , wherein said first amplification product and said second amplification product are produced sequentially.

19. The method of claim 1 , wherein each amplification product is produced by Polymerase Chain Reaction (“PCR”) amplification.