Back to results
US 2003/0198977 A1Published application
Early leukemia diagnostics using microsphere arrays
AssigneeThe Regents of the University of California
InventorsJohn P. Nolan, Feng Zhou
Life of this patent
Estimating the term…
Abstract
The present invention provides methods and kits for detecting chromosome translocations. The present invention further provides methods for diagnosing cancer.
Claims52
A method of detecting a chromosome translocation, the method comprising:
- (a) amplifying a target nucleic acid sequence from a biological sample;
- (b) hybridizing a first oligonucleotide specific for a first region of the translocation to the amplified target under conditions in which the first oligonucleotide specifically hybridizes to the first region of the translocation,
- wherein the first oligonucleotide comprises a first capture tag;
- (c) hybridizing a second oligonucleotide specific for a second region of the translocation to the amplified target under conditions in which the second oligonucleotide specifically hybridizes to the second region of the translocation,
- wherein the second oligonucleotide comprises a second capture tag;
- (d) extending the first and second hybridized oligonucleotide sequences to produce a first and a second labeled extended oligonucleotide;
- (e) hybridizing the first and second oligonucleotides to a first and a second address tag on a solid support under conditions in which the first and second address tags specifically hybridize to the first and second capture tags;
- and
- (f) detecting the presence of the first and second labeled extended oligonucleotides on the solid support, thereby detecting the presence of the chromosome translocation.
6 more elements
A kit for detecting a chromosome translocation, the kit comprising:
- a first oligonucleotide specific for a first region of the translocation and a second oligonucleotide specific for a second region of the translocation, wherein each oligonucleotide comprises a capture tag comprising a polynucleotide sequence.
A method for diagnosing cancer by detecting a chromosome translocation pattern, the method comprising:
- (a) amplifying a target nucleic acid from a biological sample;
- (b) hybridizing a first oligonucleotide specific for a first region of the translocation to the amplified target under conditions in which the first oligonucleotide specifically hybridizes to the first region of the translocation,
- wherein the first oligonucleotide comprises a first capture tag;
- (c) hybridizing a second oligonucleotide specific for a second region of the translocation to the amplified target under conditions in which the second oligonucleotide specifically hybridizes to the second region of the translocation,
- wherein the second oligonucleotide comprises second a capture tag;
- (d) hybridizing a third oligonucleotide specific for a junction region within the translocation to the amplified target under conditions in which the third oligonucleotide specifically hybridizes to the junction region,
- wherein the third oligonucleotide comprises a third capture tag;
- (e) extending the first, second, and third hybridized oligonucleotide sequences to produce a first, second, and third labeled extended oligonucleotide;
- (f) hybridizing the first, second, and third oligonucleotides to a first, a second, and a third address tag on a solid support under conditions in which the first, second, and third labeled extended oligonucleotides specifically hybridize to the first, second, and third address tag;
- and
- (g) detecting the presence of the first, second, and third labeled extended oligonucleotides on the solid support, thereby detecting the presence of the chromosome translocation.
8 more elements
A method of detecting a chromosome translocation, the method comprising:
- (a) amplifying a target nucleic acid sequence from a biological sample;
- (b) hybridizing a first oligonucleotide specific for a first region of the translocation to the amplified target under conditions in which the first oligonucleotide specifically hybridizes to the first region of the translocation,
- wherein the first oligonucleotide comprises a label;
- (c) hybridizing a second oligonucleotide specific for a second region of the translocation to the amplified target under conditions in which the second oligonucleotide specifically hybridizes to the second region of the translocation,
- wherein the second oligonucleotide comprises a capture tag;
- (d) ligating the first and second oligonucleotide to each other;
- (e) hybridizing the first and second oligonucleotides to an address tag on a solid support under conditions in which the address tag specifically hybridizes to the capture tag;
- and
- (f) detecting the presence of the ligated first and second oligonucleotides on the solid support, thereby detecting the presence of the chromosome translocation.
6 more elements
An isolated nucleic acid comprising any one of the sequences set forth in SEQ ID NOS:
- 1-103.
Dependencies are inferred from the claim text.