Mapping of genomic interactions

1. A method, comprising;

a) contacting deoxyribonucleic acid with a cross-linking agent under conditions such that interacting chromatin segments are cross-linked;

b) digesting said cross-linked chromatin segments to generate digested chromatin segments;

c) ligating said digested chromatin segments to generate a first genomic interaction library comprising a plurality of ligation products;

d) contacting said plurality of ligation products with a plurality of unique primers under conditions such that ligation mediated amplification generates a second genomic interaction library that is a copy of a part of said first genomic interaction library; and

e) amplifying said second genomic library with a single pair of PCR primers.

2. The method of claim 1 , wherein said plurality of unique primer pairs comprises at least 10 unique primer pairs.

3. The method of claim 1 , wherein said plurality of unique primer pairs comprises at least 100 unique primer pairs.

4. The method of claim 1 , wherein said plurality of unique primer pairs comprises at least 500 unique primer pairs.

5. The method of claim 1 , wherein said plurality of unique primers pairs comprises at least 1000 unique primer pairs.

6. The method of claim 1 , wherein said plurality of unique primers pairs comprises at least 10,000 unique primer pairs.

7. The method of claim 1 , wherein said plurality of unique primers pairs comprises at least 100,000 unique primer pairs.

8. The method of claim 1 , wherein said genomic interaction library comprises ligated deoxyribonucleic acids approximately 100 bps in length.

9. The method of claim 1 , wherein said second interaction library is representative of long-range genomic interactions.

10. The method of claim 9 , wherein said long-range genomic interactions comprise interaction of activators or repressors of gene expression with a gene.

11. The method of claim 9 , wherein said long-range genomic interactions comprise interaction of chromatin on different chromosomes.

12. The method of claim 1 , wherein said deoxyribonucleic acid is derived from at least one cell.

13. The method of claim 12 , wherein said at least one cell is selected from the group consisting of an animal cell, a bacterial cell and a plant cell.

14. The method of claim 9 , further comprising the step of calculating interaction frequencies for said long range genomic interactions.

15. The method of claim 1 , wherein said genomic interaction library has one or more variant genes selected from at least one of the group consisting of polymorphisms, genomic deletions, genomic fusions, genomic translocations, and genomic inversions.

16. The method of claim 1 , wherein said single pair of PCR primers is a single pair of universal primers.

17. The method of claim 1 , further comprising step (f) analyzing said amplified second genomic library with a high-throughput application.

18. The method of claim 17 , wherein said high throughput application comprises sequencing.

19. The method of claim 17 , wherein said high throughput application is performed using a microarray.