Methods, kits and compositions pertaining to the suppression of the detectable probe binding to randomly distributed repeat sequences in genomic nucleic acid

1. A method for suppressing the binding of one or more detectable nucleic acid probes to one or more undesired sequences in an assay for determining target genomic nucleic acid of a sample; said method comprising:

a) contacting the sample with a mixture of two or more different non-nucleotide probes wherein each probe is 16 to 50 nucleobases in length and each probe comprises a nucleobase sequence identical to one of the nucleobase sequences of the group consisting of: Seq. Id. No. 3, Seq. Id. No. 4, Seq. Id. No. 5, Seq. Id. No. 6, Seq. Id. No. 7, Seq. Id. No. 8, Seq. Id. No. 9, Seq. Id. No. 10, Seq. Id. No. 11, Seq. Id. No. 12, Seq. Id. No. 13, and the complement thereof, wherein the mixture of non-nucleotide probes further comprises at least one probe comprising a nucleobase sequence selected from TT(k)TTTTT(k)TTTLysOLysOTTT(k)TTTTT(k)TT and AA(k)AAAAA(k)AAALysOLysOAAA(k)AAAAA(k)AA, wherein (k) is a D-lysine, Lys is L-lysine, and O is 8-amino-3,6-dioxaoctanoic acid;

b) contacting the sample with the one or more detectable nucleic acid probes, wherein said one or more detectable nucleic acid probes is 100 bp or greater, is derived from a genomic nucleic acid, and contains one or more segments of randomly distributed repeat sequence selected from the group consisting of SINEs and LINEs; and

c) determining the target genomic nucleic acid of the sample by determining the hybridization of the one or more detectable nucleic acid probes to the target genomic nucleic acid of the sample.

2. The method of claim 1 , wherein the two or more non-nucleotide probes are peptide nucleic acid (PNA) oligomers.

3. The method of claim 2 , wherein the PNA subunits of the individual PNA oligomers have the formula:

wherein,

each J is the same or different and is selected from the group consisting of: H, R 1 , OR 1 , SR 1 , NHR 1 , NR 1 2 , F, Cl, Br and I;

each K is the same or different and is selected from the group consisting of: O, S, NH and NR 1 ;

each R 1 is the same or different and is an alkyl group having one to five carbon atoms which may optionally contain a heteroatom or a substituted or unsubstituted aryl group;

each A is selected from the group consisting of a single bond, a group of the formula: —(CJ 2 ) s - and a group of the formula; —(CJ 2 ) s C(O)— wherein, J is defined above and each s is an integer from one to five;

each t is 1 or 2;

each u is 1 or 2; and

each L is the same or different and is independently selected from the group consisting of J, dabcyl, fluorescein, adenine, cytosine, guanine, thymine, uracil, 5-propynyl-uracil, 2-thio-5-propynyl-uracil, 5-methylcytosine, 2-aminopurine, 2-amino-6-chloropurine, 2,6-diaminopurine, hypoxanthine, pseudoisocytosine, 2-thiouracil, 2-thiothymidine, N9-(2-amino-6-chloropurine), N9-(2,6-diaminopurine), N9-(7-deaza-guanine), N9-(7-deaza-8-aza-guanine) and N8-(7-deaza-8-aza-adenine), other naturally occurring nucleobase analogs, other non-naturally occurring nucleobases and substituted and unsubstituted aromatic moieties.

4. The method of claim 3 , wherein the PNA subunits of the individual PNA probes consist of a naturally or non-naturally occurring nucleobase attached to an aza nitrogen of an N-[2-(aminoethyl)]glycine backbone through a methylene carbonyl linkage.

5. The method of claim 1 , wherein the mixture comprises 5 to about 50 different non-nucleotide probes.

6. The method of claim 5 , wherein the mixture comprises about 10 to about 25 different probes.

7. The method of claim 1 , wherein the one or more detectable nucleic acid probes(s) is labeled with a fluorophore.