Detection of nucleic acid sequence differences by comparative genomic hybridization

• US 7,534,567 B2
• Filed: 02/16/2005
• Issued: 05/19/2009
• Est. Priority Date: 03/04/1992
• Status: Expired due to Term

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Waldman, Frederic, Pinkel, Daniel, Gray, Joe W., Kallioniemi, Anne, Fridyland, Jane, Huey, Bing, Albertson, Donna G., Snijders, Antoine, Kallioniemi, Olli-Pekka
• Primary Examiner(s): Horlick; Kenneth R.
• Assistant Examiner(s): Thomas; David C
• Application Number:
  US11/060,644
• Publication Number:
  US 20060063168A1
• Time in Patent Office: 1,553 Days
• Field of Search: None
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6841 In situ hybridisation
• CPC Class Codes: C12Q 2565/601 being a microscope, e.g. atomic force microscopy [AFM]
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers

Abstract

The present invention provides a method of detecting nucleotide sequence differences between two nucleic acid samples. The method employs a comparative genomic hybridization (CGH) technique to analyze the sequence differences between the samples. This method permits the identification of small sequence differences (e.g., sequence divergence of 1% or less) in nucleic acid samples of high complexity (e.g., an entire genome).

Claims

1. A method of detecting one or more nucleotide sequence differences in nucleic acid sequences in a first sample relative to nucleic acid sequences in a second sample, said method comprising:

(a) labeling nucleic acids from each sample with a different label;

(b) contacting the labeled nucleic acids from each sample with target nucleic acids, wherein either the labeled nucleic acids or the target nucleic acids, or both, have had repetitive sequences, if initially present, blocked and/or removed; and

(c) comparing the intensities of the signals from labeled nucleic acids hybridized to the target nucleic acids to detect one or more nucleotide sequence differences between the samples.

2. The method of claim 1, wherein the labeled nucleic acids from each sample are contacted with the target nucleic acids simultaneously.

3. The method of claim 1, wherein said comparing comprises determining the ratio of signal intensity of the labeled nucleic acids from said first and second samples hybridized to each target nucleic acid.

4. The method of claim 3, wherein said comparing additionally comprises comparing the ratio for one target nucleic acid with the ratio for another target nucleic acid.

5. The method of claim 1, wherein the target nucleic acids comprise DNA molecules.

6. The method of claim 5, wherein the target nucleic acids comprise genomic DNA molecules.

7. The method of claim 1, wherein the samples are derived from different species.

8. The method of claim 1, wherein the samples are derived from the same species.

9. The method of claim 1, wherein the labeled nucleic acids from at least one sample comprise the genome of an organism.

10. The method of claim 1, wherein the one or more nucleotide sequence differences detected comprise loss of heterozygosity at one or more loci in the first sample relative to the second sample.

11. The method of claim 10, wherein the samples are derived from the same species.