Ex Parte Friddle et al - Page 15


                Appeal No. 2005-0731                                                                       Page 15                             
                Application No. 09/974,712                                                                                                     

                specification at or about page 3, line 10; page 11, line 26 and page 19, line 9).”  The                                        
                sentences including those lines read as follows:                                                                               
                         • “The sequences of the present invention are also useful as additional DNA                                           
                             markers for restriction fragment length polymorphism (RFLP) analysis, and in                                      
                             forensic biology.”  Page 3, lines 8-10;                                                                           
                         •   “In addition, the sequences of the present invention can be used to provide                                       
                             polynucleotide reagents, e.g., PCR primers, targeted to specific loci in the                                      
                             human genome, which can enhance the reliability of DNA-based forensic                                             
                             identifications by, for example, providing another ‘identification marker’ (i.e.,                                 
                             another DNA sequence that is unique to a particular individual).”  Page 11,                                       
                             lines 23-28; and                                                                                                  
                         •  “These uses include but are not limited to the generation of antibodies, as                                        
                             reagents in diagnostic assays, the identification of other cellular gene                                          
                             products related to NHP, as reagents in assays for screening for compounds                                        
                             that can be used as pharmaceutical reagents useful in the therapeutic                                             
                             treatment of mental, biological, or medical disorders and diseases.”  Page 19,                                    
                             lines 7-13.                                                                                                       
                         We do not find those passages to support the asserted utility.  In each of the                                        
                cited passages, the specification is discussing uses for the claimed DNA itself or the                                         
                protein encoded by the claimed DNA.  Appellants have pointed to nothing in the                                                 
                specification that discloses that the polymorphisms in the DNA are useful in, e.g.,                                            
                forensic analysis.                                                                                                             
                         In addition, even assuming that those skilled in the art would have understood                                        
                the cited passages to refer to the use of the polymorphisms in forensic analysis,                                              
                Appellants have not shown that the skilled worker would have found the specific                                                
                polymorphisms present in SEQ ID NO:1 – without analysis of their degree of variability                                         
                in the human population and without associating them with any other genetic marker –                                           
                to be useful as argued.  Thus, the polymorphism-based utility asserted in the Appeal                                           
                Brief lacks evidentiary support and cannot be relied on to overcome the rejection.                                             






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