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| Application No. | Application Title | Issue Date |
| 20110130296 | MULTI-GENE CLASSIFIERS AND PROGNOSTIC INDICATORS FOR CANCERS The present invention relates to the identification of marker genes useful in the diagnosis and prognosis of clinically problematic subsets of primary breast cancers. More specifically, the invention relates to the identification of two sets of marker genes that are dif... | 06/02/2011 |
| 20100279876 | DETECTION OF NUCLEIC ACID SEQUENCE DIFFERENCES BY COMPARATIVE GENOMIC HYBRIDIZATION 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... | 11/04/2010 |
| 20060292608 | Comparative genomic hybridization Disclosed are new methods comprising the use of in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed a... | 12/28/2006 |
| 20060257895 | Detection of chromosomal abnormalities associated with breast cancer Disclosed are new methods comprising the use of in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed a... | 11/16/2006 |
| 20060063168 | Detection of nucleic acid sequence differences by comparative genomic hybridization 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... | 03/23/2006 |
| 20050118634 | Comparative genomic hybridization Disclosed are new methods comprising the use of in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed a... | 06/02/2005 |
