The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Aug. 01, 2006
Filed:
Sep. 26, 2001
Francis Barany, New York, NY (US);
George Barany, Falcon Heights, MN (US);
Robert P. Hammer, Baton Rouge, LA (US);
Maria Kempe, Minneapolis, MN (US);
Herman Blok, Wemeldinge, NL;
Monib Zirvi, New York, NY (US);
Francis Barany, New York, NY (US);
George Barany, Falcon Heights, MN (US);
Robert P. Hammer, Baton Rouge, LA (US);
Maria Kempe, Minneapolis, MN (US);
Herman Blok, Wemeldinge, NL;
Monib Zirvi, New York, NY (US);
Cornell Research Foundation, Inc., Ithaca, NY (US);
Board of Supervisors of Louisiana State University and Agricultural and Mechanical College, Baton Rouge, LA (US);
Regents of the University of Minnesota, Minneapolis, MN (US);
Abstract
The present invention describes a method for identifying one or more of a plurality of sequences differing by one or more single base changes, insertions, deletions, or translocations in a plurality of target nucleotide sequences. The method includes a ligation phase, a capture phase, and a detection phase. The ligation phase utilizes a ligation detection reaction between one oligonucleotide probe, which has a target sequence-specific portion and an addressable array-specific portion, and a second oligonucleotide probe, having a target sequence-specific portion and a detectable label. After the ligation phase, the capture phase is carried out by hybridizing the ligated oligonucleotide probes to a solid support with an array of immobilized capture oligonucleotides at least some of which are complementary to the addressable array-specific portion. Following completion of the capture phase, a detection phase is carried out to detect the labels of ligated oligonucleotide probes hybridized to the solid support. The ligation phase can be preceded by an amplification process. The present invention also relates to a kit for practicing this method, a method of forming arrays on solid supports, and the supports themselves.