Method For Detecting at Least One Designated Genetic Sequence

1 . A method for detecting at least one designated genetic sequence in a biological sample comprising:

a) treating said biological sample to obtain a lysate containing cellular debris including a genomic nucleic acid, wherein genomic said nucleic acid includes at least a portion of an intact nucleic acid;

b) separating a standard concentration of genomic nucleic acid using magnetic particles; and

c) screening said standard concentration of genomic nucleic acid to detect said designated genetic sequence.

2 . The method of claim 1 , wherein the step of separating a standard concentration of genomic nucleic acid includes the step of treating said lysate to saturate said magnetic particles with genomic nucleic acid.

3 . The method of claim 2 wherein the step of separating a standard concentration of genomic nucleic acid includes the step of:

(a) separating said genomic nucleic acid from said cellular debris using magnetic particles, and

(b) adding an elution solution to disassociate a standard concentration of genomic nucleic acid from said magnetic particles.

4 . The method of claim 2 wherein the step of treating said lysate to saturate said magnetic particles includes adding a sufficient amount of chaotropic salt to bind said genomic nucleic acid to said magnetic particles.

5 . The method of claim 1 further comprising the step of processing said genomic nucleic acid to be single stranded.

6 . The method of claim 2 wherein the elution solution is nuclease free water.

7 . The method of claim 1 wherein said biological sample is tissue biopsy.

8 . The method of claim 1 wherein said biological sample is fecal matter.

9 . The method of claim 1 wherein said biological sample is embryonic tissue.

10 . The method of claim 1 wherein said biological sample is bone marrow.

11 . The method of claim 1 wherein said biological sample is embryonic stem cells.

12 . The method of claim 1 wherein said biological sample is from a human.

13 . The method of claim 1 wherein the step of treating said biological sample to obtain a lysate includes treating said biological sample with a sufficient amount of lysis reagent.

14 . The method of claim 1 wherein the step of treating said biological sample to obtain a lysate includes treating said biological sample with a sufficient amount of proteinase K.

15 . The method of claim 1 wherein said biological sample contains a virus.

16 . The method of claim 1 wherein said standard concentration of said genomic nucleic acid is about 0.2 O.D. units in a 50 μl path length.

17 . A method for detecting at least one designated genetic sequence in a biological sample comprising:

a) treating said biological sample to obtain a lysate containing cellular debris including a genomic nucleic acid, wherein said genomic nucleic acid includes at least a portion of intact nucleic acid;

b) separating said genomic nucleic acid using magnetic particles;

c) adding at least one probe and primer set corresponding to one of said at least one designated genetic sequence to said biological sample in said at least one well of a microwell container;

d) adding at least one probe and primer set corresponding to a reference sequence to said biological sample in said at least one well of a microwell container;

e) screening said biological sample in said at least one well of a microwell container to obtain screening results, wherein one of said screening results is probe values; and

f) comparing the probe values for said probe corresponding to said designated genetic sequence with said probe value corresponding to said reference sequence to detect said at least one designated genetic sequence.

18 . The method of claim 17 wherein said biological sample is blood.

19 . The method of claim 17 wherein the probe corresponding to said reference sequence probe is SEQ ID NO. 21.